LRRK2 - leucine rich repeat kinase 2 Gene

Also Known as PARK8; RIPK7; ROCO2; AURA17; DARDARIN

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 120892

About LRRK2

Cytogenetic location: 12q12 Genomic coordinates (GRCh38): 12:40,224,997-40,369,285 (from NCBI)

This gene has 21 transcripts (splice variants), 191 orthologues, 23 paralogues and is associated with 3 phenotypes. Broad expression in lung (RPKM 31.3), appendix (RPKM 7.6) and 15 other tissues.

Summary

This gene is a member of the leucine-rich repeat kinase family and encodes a protein with an ankryin repeat region, a leucine-rich repeat (LRR) domain, a kinase domain, a DFG-like motif, a Ras domain, a GTPase domain, a MLK-like domain, and a WD40 domain. The protein is present largely in the cytoplasm but also associates with the mitochondrial outer membrane. Mutations in this gene have been associated with Parkinson disease-8. [provided by RefSeq, Jul 2008]

LRRK2 Products (12)

mRNA Protein Name
XR_007063041.1
NM_198578.4 NP_940980.4 leucine-rich repeat serine/threonine-protein kinase 2
XM_024448833.2 XP_024304601.1 leucine-rich repeat serine/threonine-protein kinase 2 isoform X5
XM_011537877.4 XP_011536179.1 leucine-rich repeat serine/threonine-protein kinase 2 isoform X2
XM_047428278.1 XP_047284234.1 leucine-rich repeat serine/threonine-protein kinase 2 isoform X4
XM_047428277.1 XP_047284233.1 leucine-rich repeat serine/threonine-protein kinase 2 isoform X3
XM_017018787.2 XP_016874276.1 leucine-rich repeat serine/threonine-protein kinase 2 isoform X9
XM_017018786.3 XP_016874275.1 leucine-rich repeat serine/threonine-protein kinase 2 isoform X8
XM_011537881.4 XP_011536183.1 leucine-rich repeat serine/threonine-protein kinase 2 isoform X7
XM_005268629.5 XP_005268686.1 leucine-rich repeat serine/threonine-protein kinase 2 isoform X1
XM_011537882.4 XP_011536184.1 leucine-rich repeat serine/threonine-protein kinase 2 isoform X10
XM_047428279.1 XP_047284235.1 leucine-rich repeat serine/threonine-protein kinase 2 isoform X6
Molecular Function GO Annotation Evidence References Source
enables GTP binding IDA
IDA: Inferred from direct assay
16980962 GOA
enables GTP-dependent protein kinase activity IDA
IDA: Inferred from direct assay
17260967 GOA
enables GTP-dependent protein kinase activity IMP
IMP: Inferred from mutant phenotype
17200152 GOA
enables GTPase activator activity IDA
IDA: Inferred from direct assay
17442267 GOA
enables GTPase activity IDA
IDA: Inferred from direct assay
21048939 GOA
enables JUN kinase kinase kinase activity IDA
IDA: Inferred from direct assay
19302196 GOA
enables MAP kinase kinase kinase activity IDA
IDA: Inferred from direct assay
19302196 GOA
enables SNARE binding IPI
IPI: Inferred from physical interaction
21307259 GOA
enables actin binding IPI
IPI: Inferred from physical interaction
21307259 GOA
enables clathrin binding IPI
IPI: Inferred from physical interaction
21307259 GOA
enables identical protein binding IPI
IPI: Inferred from physical interaction
16321986 GOA
enables kinase activity IDA
IDA: Inferred from direct assay
17114044 GOA
enables kinase activity IMP
IMP: Inferred from mutant phenotype
23916833 GOA
enables magnesium ion binding IMP
IMP: Inferred from mutant phenotype
28720718 GOA
enables peroxidase inhibitor activity IDA
IDA: Inferred from direct assay
21850687 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
16321986 GOA
enables protein homodimerization activity IPI
IPI: Inferred from physical interaction
16321986 GOA
enables protein kinase A binding IPI
IPI: Inferred from physical interaction
24464040 GOA
enables protein kinase activity IDA
IDA: Inferred from direct assay
16269541 GOA
enables protein serine/threonine kinase activity EXP
EXP: Inferred from Experiment
26751287 GOA
enables protein serine/threonine kinase activity IDA
IDA: Inferred from direct assay
17200152 GOA
enables protein serine/threonine kinase activity IMP
IMP: Inferred from mutant phenotype
28720718 GOA
enables signaling receptor complex adaptor activity IDA
IDA: Inferred from direct assay
22899650 GOA
enables small GTPase binding IPI
IPI: Inferred from physical interaction
21048939 GOA
enables syntaxin-1 binding IPI
IPI: Inferred from physical interaction
21307259 GOA
enables transmembrane transporter binding IPI
IPI: Inferred from physical interaction
21370995 GOA
enables tubulin binding IDA
IDA: Inferred from direct assay
21159966 GOA
Biological Process GO Annotation Evidence References Source
involved in GTP metabolic process IDA
IDA: Inferred from direct assay
21048939 GOA
involved in Golgi organization IMP
IMP: Inferred from mutant phenotype
24510904 GOA
involved in JNK cascade IDA
IDA: Inferred from direct assay
19302196 GOA
involved in MAPK cascade IDA
IDA: Inferred from direct assay
17200152 GOA
involved in Rho protein signal transduction IDA
IDA: Inferred from direct assay
25500533 GOA
involved in Wnt signalosome assembly IPI
IPI: Inferred from physical interaction
22899650 GOA
involved in calcium-mediated signaling IMP
IMP: Inferred from mutant phenotype
25416817 GOA
involved in cellular response to dopamine IMP
IMP: Inferred from mutant phenotype
23628791 GOA
involved in cellular response to manganese ion IMP
IMP: Inferred from mutant phenotype
23628791 GOA
involved in cellular response to oxidative stress IMP
IMP: Inferred from mutant phenotype
21362567 GOA
involved in cellular response to reactive oxygen species IMP
IMP: Inferred from mutant phenotype
24576675 GOA
involved in cellular response to starvation IMP
IMP: Inferred from mutant phenotype
24211199 GOA
involved in determination of adult lifespan IMP
IMP: Inferred from mutant phenotype
19692353 GOA
involved in endocytosis IGI
IGI: Inferred from genetic interaction
24576675 GOA
involved in endocytosis IMP
IMP: Inferred from mutant phenotype
24576675 GOA
involved in endoplasmic reticulum organization IMP
IMP: Inferred from mutant phenotype
25201882 GOA
involved in exploration behavior IMP
IMP: Inferred from mutant phenotype
20659558 GOA
involved in intracellular distribution of mitochondria IMP
IMP: Inferred from mutant phenotype
21159966 GOA
involved in lysosome organization IMP
IMP: Inferred from mutant phenotype
25416817 GOA
involved in mitochondrion localization IMP
IMP: Inferred from mutant phenotype
22764206 GOA
involved in mitochondrion organization IMP
IMP: Inferred from mutant phenotype
22764206 GOA
acts upstream of or within negative regulation of GTPase activity IDA
IDA: Inferred from direct assay
22423108 GOA
involved in negative regulation of autophagosome assembly IMP
IMP: Inferred from mutant phenotype
23916833 GOA
involved in negative regulation of endoplasmic reticulum stress-induced intrinsic apoptotic signaling pathway IMP
IMP: Inferred from mutant phenotype
21857923 GOA
involved in negative regulation of macroautophagy IMP
IMP: Inferred from mutant phenotype
19640926 GOA
involved in negative regulation of protein binding IMP
IMP: Inferred from mutant phenotype
23949442 GOA
involved in negative regulation of protein processing IDA
IDA: Inferred from direct assay
21370995 GOA
involved in negative regulation of protein targeting to mitochondrion IDA
IDA: Inferred from direct assay
21370995 GOA
involved in negative regulation of thioredoxin peroxidase activity by peptidyl-threonine phosphorylation IDA
IDA: Inferred from direct assay
21850687 GOA
involved in neuromuscular junction development IMP
IMP: Inferred from mutant phenotype
21159966 GOA
involved in neuron projection morphogenesis IMP
IMP: Inferred from mutant phenotype
17114044 GOA
involved in olfactory bulb development IMP
IMP: Inferred from mutant phenotype
21168496 GOA
involved in peptidyl-serine phosphorylation IDA
IDA: Inferred from direct assay
19576176 GOA
involved in peptidyl-threonine phosphorylation IDA
IDA: Inferred from direct assay
21048939 GOA
involved in peptidyl-threonine phosphorylation IMP
IMP: Inferred from mutant phenotype
23949442 GOA
involved in phosphorylation IMP
IMP: Inferred from mutant phenotype
23916833 GOA
involved in positive regulation of MAP kinase activity IMP
IMP: Inferred from mutant phenotype
21857923 GOA
involved in positive regulation of autophagy IMP
IMP: Inferred from mutant phenotype
22012985 GOA
involved in positive regulation of canonical Wnt signaling pathway IGI
IGI: Inferred from genetic interaction
22899650 GOA
involved in positive regulation of dopamine receptor signaling pathway IMP
IMP: Inferred from mutant phenotype
20659558 GOA
involved in positive regulation of programmed cell death IDA
IDA: Inferred from direct assay
17200152 GOA
involved in positive regulation of protein autoubiquitination IDA
IDA: Inferred from direct assay
16352719 GOA
involved in positive regulation of protein binding IDA
IDA: Inferred from direct assay
21370995 GOA
involved in positive regulation of protein kinase activity IDA
IDA: Inferred from direct assay
19302196 GOA
involved in positive regulation of protein phosphorylation IDA
IDA: Inferred from direct assay
22012985 GOA
involved in positive regulation of protein phosphorylation IMP
IMP: Inferred from mutant phenotype
20659558 GOA
involved in positive regulation of protein ubiquitination IDA
IDA: Inferred from direct assay
16352719 GOA
involved in protein autophosphorylation IDA
IDA: Inferred from direct assay
16269541 GOA
involved in protein autophosphorylation IMP
IMP: Inferred from mutant phenotype
16980962 GOA
involved in protein localization to endoplasmic reticulum exit site IMP
IMP: Inferred from mutant phenotype
25201882 GOA
involved in protein phosphorylation IMP
IMP: Inferred from mutant phenotype
23628791 GOA
involved in regulation of CAMKK-AMPK signaling cascade IMP
IMP: Inferred from mutant phenotype
22012985 GOA
involved in regulation of autophagy IMP
IMP: Inferred from mutant phenotype
24211199 GOA
involved in regulation of branching morphogenesis of a nerve IMP
IMP: Inferred from mutant phenotype
21168496 GOA
involved in regulation of dendritic spine morphogenesis IMP
IMP: Inferred from mutant phenotype
21168496 GOA
involved in regulation of locomotion IMP
IMP: Inferred from mutant phenotype
19692353 GOA
involved in regulation of lysosomal lumen pH IMP
IMP: Inferred from mutant phenotype
22012985 GOA
involved in regulation of membrane potential IMP
IMP: Inferred from mutant phenotype
21159966 GOA
involved in regulation of mitochondrial depolarization IMP
IMP: Inferred from mutant phenotype
22736029 GOA
involved in regulation of neuroblast proliferation IMP
IMP: Inferred from mutant phenotype
21168496 GOA
involved in regulation of neuron maturation IMP
IMP: Inferred from mutant phenotype
21168496 GOA
involved in regulation of protein stability IMP
IMP: Inferred from mutant phenotype
26014385 GOA
involved in regulation of reactive oxygen species metabolic process IMP
IMP: Inferred from mutant phenotype
24576675 GOA
involved in regulation of retrograde transport, endosome to Golgi IGI
IGI: Inferred from genetic interaction
23395371 GOA
involved in regulation of synaptic vesicle exocytosis IMP
IMP: Inferred from mutant phenotype
23949442 GOA
involved in response to oxidative stress IMP
IMP: Inferred from mutant phenotype
19692353 GOA
involved in tangential migration from the subventricular zone to the olfactory bulb IMP
IMP: Inferred from mutant phenotype
21168496 GOA
Cellular Component GO Annotation Evidence References Source
located in Golgi apparatus IDA
IDA: Inferred from direct assay
23395371 GOA
located in Golgi-associated vesicle IDA
IDA: Inferred from direct assay
24510904 GOA
part of Wnt signalosome IDA
IDA: Inferred from direct assay
22899650 GOA
located in amphisome IDA
IDA: Inferred from direct assay
19640926 GOA
located in autolysosome IDA
IDA: Inferred from direct assay
19640926 GOA
located in axon IDA
IDA: Inferred from direct assay
17120249 GOA
located in caveola neck IDA
IDA: Inferred from direct assay
19640926 GOA
located in cytoplasm IDA
IDA: Inferred from direct assay
16321986 GOA
located in cytoplasm IMP
IMP: Inferred from mutant phenotype
26014385 GOA
located in cytoplasmic side of mitochondrial outer membrane IDA
IDA: Inferred from direct assay
16269541 GOA
located in cytosol IDA
IDA: Inferred from direct assay
21850687 GOA
located in dendrite IDA
IDA: Inferred from direct assay
17120249 GOA
located in dendrite cytoplasm IDA
IDA: Inferred from direct assay
21696411 GOA
located in endoplasmic reticulum IDA
IDA: Inferred from direct assay
19640926 GOA
located in endoplasmic reticulum exit site IDA
IDA: Inferred from direct assay
25201882 GOA
located in growth cone IDA
IDA: Inferred from direct assay
19625296 GOA
located in microvillus IDA
IDA: Inferred from direct assay
19640926 GOA
located in mitochondrial membrane IDA
IDA: Inferred from direct assay
22736029 GOA
located in mitochondrion IDA
IDA: Inferred from direct assay
21850687 GOA
located in multivesicular body, internal vesicle IDA
IDA: Inferred from direct assay
19640926 GOA
located in neuron projection IDA
IDA: Inferred from direct assay
19625296 GOA
located in neuronal cell body IDA
IDA: Inferred from direct assay
21048939 GOA
located in perikaryon IDA
IDA: Inferred from direct assay
17120249 GOA
located in plasma membrane IDA
IDA: Inferred from direct assay
22899650 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

LRRK2 Protein Structure

LRR_8

LRR_8: Leucine rich repeat (984 - 1047)

LRR_1

LRR_1: Leucine Rich Repeat (1131 - 1151)

LRR_4

LRR_4: Leucine Rich repeats (2 copies) (1247 - 1281)

Roc

Roc: Ras of Complex, Roc, domain of DAPkinase (1336 - 1455)

Pkinase

Pkinase: Protein kinase domain (1885 - 2129)

  • 0
  • 400
  • 800
  • 1200
  • 1600
  • 2000
  • 2400
  • 2527 a.a.
Protein Preferred Names Protein Names

leucine-rich repeat serine/threonine-protein kinase 2

  • augmented in rheumatoid arthritis 17

LRRK2 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
LRRK2 Q5S007 CSNK1A1 Homo sapiens P48729-1 25500533
Intra
LRRK2 Q5S007 AP3B1 Homo sapiens O00203 27424887
Intra
LRRK2 Q5S007 AP3B1 Homo sapiens O00203
TAP
24725412
Intra
LRRK2 Q5S007 USP39 Homo sapiens Q53GS9 31046837
Intra
LRRK2 Q5S007 RAB1B Homo sapiens Q9H0U4 31046837
Intra
LRRK2 Q5S007 RAB1B Homo sapiens Q9H0U4 26824392
Intra
LRRK2 Q5S007 RAB1B Homo sapiens Q9H0U4 32227113
Intra
LRRK2 Q5S007 CFAP20 Homo sapiens Q9Y6A4 31046837
Intra
LRRK2 Q5S007 RPS11 Homo sapiens P62280
TAP
24725412
Intra
LRRK2 Q5S007 RPS11 Homo sapiens P62280 31046837
Intra
LRRK2 Q5S007 RPS11 Homo sapiens P62280 24725412
Intra
LRRK2 Q5S007 PPP2R2A Homo sapiens P63151 31046837
Intra
LRRK2 Q5S007 PPP2R2A Homo sapiens P63151 26894577
Intra
LRRK2 Q5S007 PPP2R2A Homo sapiens P63151 26894577
Intra
LRRK2 Q5S007 LRRK1 Homo sapiens Q38SD2 20144646
Intra
LRRK2 Q5S007 ZRANB2 Homo sapiens O95218 23075850
Intra
LRRK2 Q5S007 RPL34 Homo sapiens P49207 31046837
Intra
LRRK2 Q5S007 PAK6 Homo sapiens Q9NQU5 24510904
Intra
LRRK2 Q5S007 OPA1 Homo sapiens O60313 31046837
Intra
LRRK2 Q5S007 OPA1 Homo sapiens O60313 24282027
Intra
LRRK2 Q5S007 TTC27 Homo sapiens Q6P3X3 31046837
Intra
LRRK2 Q5S007 WSB1 Homo sapiens Q9Y6I7 27273569
Intra
LRRK2 Q5S007 WSB1 Homo sapiens Q9Y6I7
Y2H
27273569
Intra
LRRK2 Q5S007 MRPL19 Homo sapiens P49406 31046837
Intra
LRRK2 Q5S007 AHCYL1 Homo sapiens O43865 31046837
Intra
LRRK2 Q5S007 LARP7 Homo sapiens Q4G0J3 31046837
Intra
LRRK2 Q5S007 NDUFAF7 Homo sapiens Q7L592 24510904
Intra
LRRK2 Q5S007 LARP4 Homo sapiens Q71RC2 31046837
Intra
LRRK2 Q5S007 CDC37 Homo sapiens Q16543 23075850
Intra
LRRK2 Q5S007 CDC37 Homo sapiens Q16543 16321986
Intra
LRRK2 Q5S007 CDC37 Homo sapiens Q16543 31046837
Intra
LRRK2 Q5S007 CDC37 Homo sapiens Q16543 20642453
Intra
LRRK2 Q5S007 CDC37 Homo sapiens Q16543 22612223
Intra
LRRK2 Q5S007 NUP133 Homo sapiens Q8WUM0
TAP
24725412
Intra
LRRK2 Q5S007 NUP133 Homo sapiens Q8WUM0 31046837
Intra
LRRK2 Q5S007 AKT1 Homo sapiens P31749 21658387
Intra
LRRK2 Q5S007 AKT1 Homo sapiens P31749 21658387
Intra
LRRK2 Q5S007 SNAPIN Homo sapiens O95295 23949442
Intra
LRRK2 Q5S007 SNAPIN Homo sapiens O95295 23949442
Intra
LRRK2 Q5S007 YWHAH Homo sapiens Q04917 29541021
Intra
LRRK2 Q5S007 YWHAH Homo sapiens Q04917 20642453
Intra
LRRK2 Q5S007 YWHAH Homo sapiens Q04917 23075850
Intra
LRRK2 Q5S007 YWHAH Homo sapiens Q04917 20642453
Intra
LRRK2 Q5S007 YWHAH Homo sapiens Q04917 31046837
Intra
LRRK2 Q5S007 SQSTM1 Homo sapiens Q13501 29519959
Intra
LRRK2 Q5S007 SQSTM1 Homo sapiens Q13501 29519959
Intra
LRRK2 Q5S007 SQSTM1 Homo sapiens Q13501
IF
29519959
Intra
LRRK2 Q5S007 SQSTM1 Homo sapiens Q13501 29519959
Intra
LRRK2 Q5S007 SQSTM1 Homo sapiens Q13501
PLA
29519959
Intra
LRRK2 Q5S007 SQSTM1 Homo sapiens Q13501 29519959
Intra
LRRK2 Q5S007 MFN2 Homo sapiens O95140 24282027
Intra
LRRK2 Q5S007 YWHAZ Homo sapiens P63104 20642453
Intra
LRRK2 Q5S007 YWHAZ Homo sapiens P63104 20642453
Intra
LRRK2 Q5S007 YWHAZ Homo sapiens P63104 23075850
Intra
LRRK2 Q5S007 YWHAZ Homo sapiens P63104 24510904
Intra
LRRK2 Q5S007 YWHAZ Homo sapiens P63104 31046837
Intra
LRRK2 Q5S007 TUBB Homo sapiens P07437 24947832
Intra
LRRK2 Q5S007 TUBB Homo sapiens P07437
Y2H
24275654
Intra
LRRK2 Q5S007 TUBB Homo sapiens P07437 24275654
Intra
LRRK2 Q5S007 TUBB Homo sapiens P07437 31046837
Intra
LRRK2 Q5S007 RPS3 Homo sapiens P23396 24725412
Intra
LRRK2 Q5S007 RPS3 Homo sapiens P23396 31046837
Intra
LRRK2 Q5S007 RPS3 Homo sapiens P23396
TAP
24725412
Intra
LRRK2 Q5S007 TUBB4B Homo sapiens P68371 31046837
Intra
LRRK2 Q5S007 TUBB4B Homo sapiens P68371
Y2H
24275654
Intra
LRRK2 Q5S007 CORO1C Homo sapiens Q9ULV4 33938021
Intra
LRRK2 Q5S007 RPS13 Homo sapiens P62277 31046837
Intra
LRRK2 Q5S007 RPS13 Homo sapiens P62277 24725412
Intra
LRRK2 Q5S007 HSPA8 Homo sapiens P11142 17400507
Intra
LRRK2 Q5S007 HSPA8 Homo sapiens P11142 29519959
Intra
LRRK2 Q5S007 HSPA8 Homo sapiens P11142 24510904
Intra
LRRK2 Q5S007 HSPA8 Homo sapiens P11142 24947832
Intra
LRRK2 Q5S007 RPS18 Homo sapiens P62269 31046837
Intra
LRRK2 Q5S007 RPS16 Homo sapiens P62249
TAP
24725412
Intra
LRRK2 Q5S007 RPS16 Homo sapiens P62249 31046837
Intra
LRRK2 Q5S007 RPS23 Homo sapiens P62266 24725412
Intra
LRRK2 Q5S007 RPS23 Homo sapiens P62266
TAP
24725412
Intra
LRRK2 Q5S007 RPS20 Homo sapiens P60866 31046837
Intra
LRRK2 Q5S007 RPS20 Homo sapiens P60866
TAP
24725412
Intra
LRRK2 Q5S007 RPL30 Homo sapiens P62888 31046837
Intra
LRRK2 Q5S007 RPL23A Homo sapiens P62750 24725412
Intra
LRRK2 Q5S007 RPL23A Homo sapiens P62750
TAP
24725412
Intra
LRRK2 Q5S007 VDAC1 Homo sapiens P21796 31046837
Intra
LRRK2 Q5S007 EEF1A2 Homo sapiens Q05639 19559761
Intra
LRRK2 Q5S007 EEF1A2 Homo sapiens Q05639 31046837
Intra
LRRK2 Q5S007 TUBB4A Homo sapiens P04350 31046837
Intra
LRRK2 Q5S007 TUBB4A Homo sapiens P04350
Y2H
24275654
Intra
LRRK2 Q5S007 TUBB4A Homo sapiens P04350 24275654
Intra
LRRK2 Q5S007 SLC25A5 Homo sapiens P05141
TAP
24725412
Intra
LRRK2 Q5S007 BAG2 Homo sapiens O95816 24510904
Intra
LRRK2 Q5S007 SLC25A6 Homo sapiens P12236 21370995
Intra
LRRK2 Q5S007 SLC25A6 Homo sapiens P12236
TAP
24725412
Intra
LRRK2 Q5S007 RPS27 Homo sapiens P42677 31046837
Intra
LRRK2 Q5S007 RPS27 Homo sapiens P42677
TAP
24725412
Intra
LRRK2 Q5S007 RPS27 Homo sapiens P42677 24725412
Intra
LRRK2 Q5S007 YWHAE Homo sapiens P62258 24947832
Intra
LRRK2 Q5S007 YWHAE Homo sapiens P62258 23075850
Intra
LRRK2 Q5S007 YWHAE Homo sapiens P62258 31046837
Intra
LRRK2 Q5S007 YWHAE Homo sapiens P62258
TAP
24725412
Intra
LRRK2 Q5S007 YWHAE Homo sapiens P62258 20642453
Intra
LRRK2 Q5S007 BAG5 Homo sapiens Q9UL15 24510904
Intra
LRRK2 Q5S007 BAG5 Homo sapiens Q9UL15 24510904
Intra
LRRK2 Q5S007 BAG5 Homo sapiens Q9UL15 24947832
Intra
LRRK2 Q5S007 TUBB6 Homo sapiens Q9BUF5 31046837
Intra
LRRK2 Q5S007 RPL14 Homo sapiens P50914
TAP
24725412
Intra
LRRK2 Q5S007 RPL14 Homo sapiens P50914 24725412
Intra
LRRK2 Q5S007 RPL13 Homo sapiens P26373
TAP
24725412
Intra
LRRK2 Q5S007 RPL13 Homo sapiens P26373 31046837
Intra
LRRK2 Q5S007 RPL13 Homo sapiens P26373 24725412
Intra
LRRK2 Q5S007 RPL10A Homo sapiens P62906 31046837
Intra
LRRK2 Q5S007 RPL10A Homo sapiens P62906 24725412
Intra
LRRK2 Q5S007 RPL10A Homo sapiens P62906
TAP
24725412
Intra
LRRK2 Q5S007 STUB1 Homo sapiens Q9UNE7 24510904
Intra
LRRK2 Q5S007 STUB1 Homo sapiens Q9UNE7 31046837
Intra
LRRK2 Q5S007 PPP1CA Homo sapiens P62136 23937259
Intra
LRRK2 Q5S007 PPP1CA Homo sapiens P62136 23937259
Intra
LRRK2 Q5S007 PPP1CA Homo sapiens P62136 23937259
Intra
LRRK2 Q5S007 SEC16A Homo sapiens O15027 25201882
Intra
LRRK2 Q5S007 SEC16A Homo sapiens O15027 25201882
Intra
LRRK2 Q5S007 SEC16A Homo sapiens O15027 31046837
Intra
LRRK2 Q5S007 LDHB Homo sapiens P07195
TAP
24725412
Intra
LRRK2 Q5S007 LDHB Homo sapiens P07195 24725412
Intra
LRRK2 Q5S007 SLC25A4 Homo sapiens P12235
TAP
24725412
Intra
LRRK2 Q5S007 YWHAB Homo sapiens P31946 20642453
Intra
LRRK2 Q5S007 YWHAB Homo sapiens P31946 20642453
Intra
LRRK2 Q5S007 YWHAB Homo sapiens P31946 24510904
Intra
LRRK2 Q5S007 YWHAG Homo sapiens P61981 23075850
Intra
LRRK2 Q5S007 YWHAG Homo sapiens P61981
ITC
28202711
Intra
LRRK2 Q5S007 YWHAG Homo sapiens P61981 20642453
Intra
LRRK2 Q5S007 YWHAG Homo sapiens P61981
FPS
28202711
Intra
LRRK2 Q5S007 YWHAG Homo sapiens P61981 20642453
Intra
LRRK2 Q5S007 YWHAG Homo sapiens P61981 24947832
Intra
LRRK2 Q5S007 YWHAQ Homo sapiens P27348 24947832
Intra
LRRK2 Q5S007 YWHAQ Homo sapiens P27348 23075850
Intra
LRRK2 Q5S007 YWHAQ Homo sapiens P27348 31046837
Intra
LRRK2 Q5S007 YWHAQ Homo sapiens P27348 20642453
Intra
LRRK2 Q5S007 YWHAQ Homo sapiens P27348 20642453
Intra
LRRK2 Q5S007 YWHAQ Homo sapiens P27348
SPR
24351927
Intra
LRRK2 Q5S007 MAPT Homo sapiens P10636-8 24113872
Intra
LRRK2 Q5S007 MAPT Homo sapiens P10636-8 22303461
Intra
LRRK2 Q5S007 MAPT Homo sapiens P10636-8 22303461
Intra
LRRK2 Q5S007 RPP25 Homo sapiens Q9BUL9 32814053
Intra
LRRK2 Q5S007 RPP25 Homo sapiens Q9BUL9 32814053
Intra
LRRK2 Q5S007 RPP25 Homo sapiens Q9BUL9 32814053
Intra
LRRK2 Q5S007 RAB29 Homo sapiens O14966
IF
24510904
Intra
LRRK2 Q5S007 RAB29 Homo sapiens O14966 24510904
Intra
LRRK2 Q5S007 RAB29 Homo sapiens O14966 24510904
Intra
LRRK2 Q5S007 RPS15 Homo sapiens P62841 26824392
Intra
LRRK2 Q5S007 RPS15 Homo sapiens P62841 24725412
Intra
LRRK2 Q5S007 RPS15 Homo sapiens P62841 24725412
Intra
LRRK2 Q5S007 RPS15 Homo sapiens P62841 24725412
Intra
LRRK2 Q5S007 RPS15 Homo sapiens P62841 24947832
Intra
LRRK2 Q5S007 GSK3B Homo sapiens P49841 24165324
Intra
LRRK2 Q5S007 GSK3B Homo sapiens P49841 24165324
Intra
LRRK2 Q5S007 NEK1 Homo sapiens Q96PY6 24510904
Cross
LRRK2 Q5S007 Dnm1 Mus musculus P39053 21307259
Cross
LRRK2 Q5S007 Dnm1 Mus musculus P39053 24687852
Intra
LRRK2 Q5S007 RAB5B Homo sapiens P61020 25605758
Intra
LRRK2 Q5S007 RAB5B Homo sapiens P61020 18445495
Intra
LRRK2 Q5S007 RAB5B Homo sapiens P61020 27314038
Intra
LRRK2 Q5S007 RAB5B Homo sapiens P61020
Y2H
18445495
Intra
LRRK2 Q5S007 RAC1 Homo sapiens P63000 21454543
Intra
LRRK2 Q5S007 BCL2 Homo sapiens P10415-1 25446991
Intra
LRRK2 Q5S007 RPS2 Homo sapiens P15880 24725412
Intra
LRRK2 Q5S007 RPS2 Homo sapiens P15880 31046837
Intra
LRRK2 Q5S007 RPS2 Homo sapiens P15880
TAP
24725412
Intra
LRRK2 Q5S007 MAP2K6 Homo sapiens P52564 20067578
Intra
LRRK2 Q5S007 SFN Homo sapiens P31947 31046837
Intra
LRRK2 Q5S007 SFN Homo sapiens P31947 28202711
Intra
LRRK2 Q5S007 SFN Homo sapiens P31947 24510904
Intra
LRRK2 Q5S007 PRKACA Homo sapiens P17612 24351927
Intra
LRRK2 Q5S007 MAP2K7 Homo sapiens O14733 20067578
Intra
LRRK2 Q5S007 FADD Homo sapiens Q13158 19176810
Intra
LRRK2 Q5S007 AGO2 Homo sapiens Q9UKV8 20671708
Intra
LRRK2 Q5S007 AGO2 Homo sapiens Q9UKV8 17400507
Intra
LRRK2 Q5S007 MSN Homo sapiens P26038 22363216
Intra
LRRK2 Q5S007 MSN Homo sapiens P26038 22952686
Intra
LRRK2 Q5S007 MSN Homo sapiens P26038 31046837
Intra
LRRK2 Q5S007 MSN Homo sapiens P26038 25009464
Intra
LRRK2 Q5S007 MSN Homo sapiens P26038 24695735
Intra
LRRK2 Q5S007 MSN Homo sapiens P26038 20642453
Intra
LRRK2 Q5S007 MSN Homo sapiens P26038 26824392
Intra
LRRK2 Q5S007 MSN Homo sapiens P26038 24904275
Intra
LRRK2 Q5S007 MSN Homo sapiens P26038 27357661
Intra
LRRK2 Q5S007 CUEDC1 Homo sapiens Q9NWM3 24510904
Intra
LRRK2 Q5S007 MAP2K3 Homo sapiens P46734 20067578
Intra
LRRK2 Q5S007 MAP2K3 Homo sapiens P46734 20173330
Intra
LRRK2 Q5S007 ARFGAP1 Homo sapiens Q8N6T3-2 22363216
Intra
LRRK2 Q5S007 ARFGAP1 Homo sapiens Q8N6T3-2 22363216
Intra
LRRK2 Q5S007 DVL1 Homo sapiens O14640-2 19625296
Intra
LRRK2 Q5S007 DVL1 Homo sapiens O14640-2 19625296
Intra
LRRK2 Q5S007 DVL1 Homo sapiens O14640-2
Y2H
19625296
Cross
LRRK2 Q5S007 Spag9 Mus musculus Q58A65 20173330
Intra
LRRK2 Q5S007 RAB38 Homo sapiens P57729 31552791
Intra
LRRK2 Q5S007 SH3GL1 Homo sapiens Q99961 31046837
Intra
LRRK2 Q5S007 SH3GL1 Homo sapiens Q99961 22998870
Intra
LRRK2 Q5S007 SPATA22 Homo sapiens Q8NHS9 32814053
Intra
LRRK2 Q5S007 SPATA22 Homo sapiens Q8NHS9 32814053
Intra
LRRK2 Q5S007 SPATA22 Homo sapiens Q8NHS9 32814053
Intra
LRRK2 Q5S007 TUBB2A Homo sapiens Q13885
Y2H
24275654
Intra
LRRK2 Q5S007 TUBB2A Homo sapiens Q13885 31046837
Intra
LRRK2 Q5S007 RGS2 Homo sapiens P41220 24794857
Intra
LRRK2 Q5S007 RGS2 Homo sapiens P41220 24794857
Intra
LRRK2 Q5S007 RGS2 Homo sapiens P41220 24794857
Intra
LRRK2 Q5S007 CHGB Homo sapiens P05060 24510904
Intra
LRRK2 Q5S007 DNM1 Homo sapiens Q05193 24282027
Intra
LRRK2 Q5S007 DNM1 Homo sapiens Q05193
Y2H
24282027
Intra
LRRK2 Q5S007 DNM1 Homo sapiens Q05193 24282027
Intra
LRRK2 Q5S007 GAK Homo sapiens O14976
IF
24510904
Intra
LRRK2 Q5S007 GAK Homo sapiens O14976 24510904
Intra
LRRK2 Q5S007 GAK Homo sapiens O14976 24510904
Intra
LRRK2 Q5S007 NFATC2 Homo sapiens Q13469 21983832
Intra
LRRK2 Q5S007 PPP1R8 Homo sapiens Q12972 31046837
Intra
LRRK2 Q5S007 PPP1R8 Homo sapiens Q12972 24510904
Intra
LRRK2 Q5S007 ARHGEF7 Homo sapiens Q14155 25500533
Intra
LRRK2 Q5S007 ARHGEF7 Homo sapiens Q14155 21048939
Intra
LRRK2 Q5S007 ARHGEF7 Homo sapiens Q14155 21048939
Intra
LRRK2 Q5S007 ECHS1 Homo sapiens P30084 24510904
Intra
LRRK2 Q5S007 ECHS1 Homo sapiens P30084 31046837
Intra
LRRK2 Q5S007 RAB8A Homo sapiens P61006 31046837
Intra
LRRK2 Q5S007 RAB8A Homo sapiens P61006 26824392
Intra
LRRK2 Q5S007 RAB8A Homo sapiens P61006 26824392
Intra
LRRK2 Q5S007 RAB8A Homo sapiens P61006 32227113
Intra
LRRK2 Q5S007 DNM1L Homo sapiens O00429 22228096
Intra
LRRK2 Q5S007 DNM1L Homo sapiens O00429 31046837
Intra
LRRK2 Q5S007 DNM1L Homo sapiens O00429 29541021
Intra
LRRK2 Q5S007 DNM1L Homo sapiens O00429 29541021
Intra
LRRK2 Q5S007 DNM1L Homo sapiens O00429 22639965
Intra
LRRK2 Q5S007 RAB10 Homo sapiens P61026 31046837
Intra
LRRK2 Q5S007 RAB10 Homo sapiens P61026 26824392
Intra
LRRK2 Q5S007 DVL3 Homo sapiens Q92997 19625296
Intra
LRRK2 Q5S007 DVL3 Homo sapiens Q92997 19625296
Intra
LRRK2 Q5S007 DVL2 Homo sapiens O14641 31046837
Intra
LRRK2 Q5S007 DVL2 Homo sapiens O14641
Y2H
19625296
Intra
LRRK2 Q5S007 TCF25 Homo sapiens Q9BQ70 31046837
Intra
LRRK2 Q5S007 BAG3 Homo sapiens O95817 24510904
Intra
LRRK2 Q5S007 PRDX3 Homo sapiens P30048 24459295
Intra
LRRK2 Q5S007 PRDX3 Homo sapiens P30048 31046837
Intra
LRRK2 Q5S007 PRDX3 Homo sapiens P30048 21850687
Intra
LRRK2 Q5S007 PRDX3 Homo sapiens P30048 21850687
Intra
LRRK2 Q5S007 PRDX3 Homo sapiens P30048 21850687
Intra
LRRK2 Q5S007 PRDX3 Homo sapiens P30048
Y2H
21850687
Intra
LRRK2 Q5S007 PRDX3 Homo sapiens P30048 21850687
Intra
LRRK2 Q5S007 MATK Homo sapiens P42679 24510904
Cross
LRRK2 Q5S007 Atp2a2 Mus musculus O55143 31046837
Cross
LRRK2 Q5S007 Stub1 Mus musculus Q9WUD1 19196961
Cross
LRRK2 Q5S007 Ckmt1 Mus musculus P30275 21370995
Cross
LRRK2 Q5S007 Ckmt1 Mus musculus P30275 21370995
Intra
LRRK2 Q5S007 SH3GL2 Homo sapiens Q99962 22998870
Intra
LRRK2 Q5S007 SH3GL2 Homo sapiens Q99962 25501810
Intra
LRRK2 Q5S007 MAPT Homo sapiens P10636-2 24113872
Intra
LRRK2 Q5S007 CDC42 Homo sapiens P60953 21048939
Intra
LRRK2 Q5S007 CDC42 Homo sapiens P60953 21048939
Cross
LRRK2 Q5S007 Rab5b Mus musculus P61021 18445495
Cross
LRRK2 Q5S007 Mfn1 Mus musculus Q811U4 24282027
Intra
LRRK2 Q5S007 LRP6 Homo sapiens O75581 22899650
Intra
LRRK2 Q5S007 LRP6 Homo sapiens O75581
Y2H
22899650
Intra
LRRK2 Q5S007 LRP6 Homo sapiens O75581
Y2H
27013965
Intra
LRRK2 Q5S007 P46821-PRO_0000018605 Homo sapiens P46821-PRO_0000018605 24754922
Intra
LRRK2 Q5S007 P46821-PRO_0000018605 Homo sapiens P46821-PRO_0000018605 24754922
Intra
LRRK2 Q5S007 RAB32 Homo sapiens Q13637 25360523
Intra
LRRK2 Q5S007 RAB32 Homo sapiens Q13637
IF
25360523
Intra
LRRK2 Q5S007 SNCA Homo sapiens P37840 23183827
Intra
LRRK2 Q5S007 SNCA Homo sapiens P37840 23183827
Intra
LRRK2 Q5S007 SNCA Homo sapiens P37840 23183827
Cross
LRRK2 Q5S007 Ywhag Rattus norvegicus P61983 24351927
Cross
LRRK2 Q5S007 Ywhag Rattus norvegicus P61983
FPS
24351927
Cross
LRRK2 Q5S007 Ywhag Rattus norvegicus P61983
SPR
24351927
Cross
LRRK2 Q5S007 Arfgap1 Rattus norvegicus Q62848 22363216
Cross
LRRK2 Q5S007 Arfgap1 Rattus norvegicus Q62848 22363216
Cross
LRRK2 Q5S007 Arfgap1 Rattus norvegicus Q62848 22363216
Cross
LRRK2 Q5S007 Arfgap1 Rattus norvegicus Q62848 22363216
Cross
LRRK2 Q5S007 phoA Escherichia coli P00634 23937259
Cross
LRRK2 Q5S007 Prkar2b Rattus norvegicus P12369 24464040
Cross
LRRK2 Q5S007 Rab29 Rattus norvegicus Q63481 23395371
Cross
LRRK2 Q5S007 MBP Bos taurus P02687 21658387
Cross: Cross-species interaction Intra: Intraspecies interaction

LRRK2 Antibodies

Cat. No. Product Name Application Reactivity
HY-P810542 Phospho-LRRK2 (Ser935) Antibody (YA9811) WB, ICC/IF, FC Human, Mouse
HY-P83076 LRRK2 Antibody (YA2821) WB, IHC-P, ICC/IF Human, Mouse
HY-P83076A Phospho-LRRK2(Ser935) Antibody (YA3424) WB, ICC/IF Human, Mouse
HY-P84632 LRRK2 Antibody (YA4329) ICC/IF, FC, ELISA Human
HY-P84632A LRRK2 Antibody (YA4329)(PBS only) ICC/IF, FC, ELISA Human
HY-P84633 LRRK2 Antibody (YA4330) IHC-P, FC, ELISA Human
HY-P84633A LRRK2 Antibody (YA4330)(PBS only) IHC-P, FC, ELISA Human

Related Diseases

Diseases Alias
Postencephalitic Parkinson Disease
  • Postencephalitic Parkinsonism

  • Parkinson Disease, Postencephalitic

Machado-Joseph Disease
  • SCA3

  • MJD

  • Spinocerebellar Ataxia 3

  • Azorean Disease

  • Spinocerebellar Ataxia Type 3

  • Azorean Neurologic Disease

  • Spinopontine Atrophy

  • Nigrospinodentatal Degeneration

  • Spinocerebellar Atrophy

  • Spinocerebellar Atrophy Iii

  • Spinocerebellar Atrophy Type 3

  • Azorean Ataxia

  • Azorean Disease Of The Nervous System

  • Machado Disease

  • Nigro-Spino-Dentatal Degeneration With Nuclear Ophthalmoplegia

  • Disease, Machado-Joseph

  • Ataxia, Spinocerebellar

Athetosis
Charcot-Marie-Tooth Disease
  • Cmt

  • Hmsn

  • Hereditary Motor And Sensory Neuropathy

  • Pma

  • Cmt - Charcot-Marie-Tooth Disease

  • Charcot Marie Tooth Disease

  • Charcot-Marie-Tooth Hereditary Neuropathy

  • Charcot-Marie-Tooth Syndrome

  • Peroneal Muscular Atrophy

  • Hereditary Motor And Sensory Neuropathies

Peripheral Nervous System Disease
  • Peripheral Neuropathy

  • Peripheral Nerve Disease

  • Peripheral Nerve Disorders

  • Neuropathy, Peripheral

  • Peripheral Neuropathy Due To Vitamin Pyridoxine Hyperalimentation

Aphasia
Dementia
  • Dementias

  • Presenile Dementia

  • Alzheimer Type Dementia

  • Alzheimer Sclerosis

  • Alzheimer Disease Dementia

  • Alzheimer Dementia

  • Primary Degenerative Alzheimer Type Dementia

  • End Stage Alzheimer'S Dementia

  • Alzheimer'S Type Atypical Dementia

  • Alzheimer Type Presenile Dementia

  • Early Onset Alzheimer Dementia

  • Dementia In Alzheimer Disease Type 2

  • Dementia In Alzheimer Disease With Early Onset

  • Early Onset Alzheimer Type Dementia, Uncomplicated

  • Primary Degenerative Alzheimer Type Dementia, Early Onset

  • Primary Degenerative Alzheimer Type Dementia, Presenile Onset, Uncomplicated

  • Alzheimer Disease Dementia With Early Onset

  • Presenile Sclerosis

  • Presenile Brain Sclerosis

  • Presenile Alzheimer Brain Sclerosis

  • Late Onset Alzheimer Dementia

  • Dementia In Alzheimer Disease Type 1

  • Dementia In Alzheimer Disease With Late Onset

  • Primary Degenerative Alzheimer Type Dementia, Late Onset

  • Sdat - [Senile Dementia, Alzheimer Type]

  • Alzheimer Disease Dementia With Late Onset

  • Late Onset Alzheimer Brain Sclerosis

  • Senile Alzheimer Brain Disease

  • Senile Alzheimer Brain Sclerosis

  • Senile Primary Degenerative Alzheimer Type Dementia

  • Senile Dementia Of The Alzheimer Type

  • Arteriosclerotic Dementia

  • Strategic-Infarct Dementia

  • Post Stroke Dementia

  • Vascular Cognitive Impairment

  • Vascular Dementia

  • Dementia Of The Lewy Body Type

  • Dementia With Lewy Bodies

  • Sdlt - [Senile Dementia Of The Lewy Body Type]

  • Senile Dementia Of The Lewy Body Type

  • Alcohol-Related Dementia

  • Alcoholic Dementia Nos

  • Alcohol-Induced Dementia

  • Alcoholic Brain Syndrome

  • Chronic Alcoholic Brain Syndrome

  • Alcohol Dementia

  • Late Onset Alcoholic Psychosis

  • Residual And Late-Onset Alcohol-Induced Psychotic Disorder

  • Mental And Behavioural Disorders Due To Use Of Sedatives Or Hypnotics, Residual And Late-Onset Psychotic Disorder

  • Late-Onset Psychoactive Substance-Induced Psychotic Disorder

  • Inhalant Dementia

  • Volatile Solvents Dementia

  • Dementia In Paralysis Agitans

  • Pdd - [Parkinson Disease Dementia]

  • Dementia Syndrome Of Parkinson Disease

  • Dementia In Parkinson Disease

  • Parkinson Related Dementia

  • Dementia In Huntington Chorea

  • Hiv - [Human Immunodeficiency Virus] Dementia

  • Hiv- [Human Immunodeficiency Virus] Associated Cognitive Motor Complex

  • Hiv- [Human Immunodeficiency Virus] Associated Dementia Complex

  • Aids - [Acquired Immunodeficiency Syndrome] Dementia Complex

  • Aids Related Dementia

  • Dementia Due To Niacin Deficiency

Rem Sleep Behavior Disorder
  • Rem Sleep Behaviour Disorder

  • Rapid Eye Movement Sleep Behavior Disorder

  • Rapid Eye Movement Sleep Behaviour Disorder

  • Rem - [Rapid Eye Movement] Behaviour Disorder

Frontotemporal Dementia
  • Pallidopontonigral Degeneration

  • Frontotemporal Lobar Degeneration

  • Semantic Dementia

  • FTD

  • Frontotemporal Lobe Dementia

  • Multiple System Tauopathy With Presenile Dementia

  • Dementia, Frontotemporal

  • Frontotemporal Dementia With Parkinsonism

  • Mstd

  • Frontotemporal Lobar Degeneration With Tau Inclusions

  • Ftld With Tau Inclusions

  • Dementia, Frontotemporal, With Parkinsonism

  • Fldem

  • Ftdp17

  • Disinhibition-Dementia-Parkinsonism-Amyotrophy Complex

  • Ddpac

  • Wilhelmsen-Lynch Disease

  • Wld

  • Ppnd

  • Dementia, Frontotemporal, With Or Without Parkinsonism

  • Semantic Primary Progressive Aphasia

  • Semantic Variant Ppa

  • Wilhemsen-Lynch Disease

  • Frontotemporal Dementia-Amyotrophic Lateral Sclerosis

  • Frontotemporal Dementia And Parkinsonism Linked To Chromosome 17

  • Ftd-Als

  • Ftld

  • Pick Complex

  • Pick Disease Of The Brain

  • Frontotemporal Dementia With Parkinsonism-17

  • Grn-Related Frontotemporal Dementia

  • Frontotemporal Dementia With Motor Neuron Disease

  • Dementia In Fronto-Temporal Lobar Degeneration

  • Ftd - [Frontotemporal Dementia]

  • Temple Dementia

  • Frontal Lobe Dementia

Nervous System Disease
  • Abnormality Of The Nervous System

  • Nervous System Diseases

  • Nervous System Disorder

Alzheimer Disease, Familial, 1
  • Alzheimer Disease

  • Alzheimer'S Disease

  • Presenile And Senile Dementia

  • AD1

  • Alzheimer Disease, Susceptibility To

  • Alzheimer Disease, Late-Onset, Susceptibility To

  • Alzheimer Disease 1, Familial

  • AD

  • Familial Alzheimer Disease

  • Alzheimer Disease, Late-Onset

  • Alzheimers Dementia

  • Alzheimer Dementia

  • Alzheimer Sclerosis

  • Alzheimer Syndrome

  • Alzheimer-Type Dementia

  • Dat

  • Primary Senile Degenerative Dementia

  • Sdat

  • Alzheimer Disease 1

  • Autosomal Dominant Alzheimer Disease

  • Early-Onset Alzheimer Disease With Cerebral Amyloid Angiopathy

  • Late Onset Alzheimer Disease

  • Alzheimers Disease

  • Alzheimer Disease, Early-Onset, With Cerebral Amyloid Angiopathy

  • Late-Onset Alzheimers Disease

  • Alzheimer'S Disease Pathway Kegg

  • Dementia Due To Alzheimer'S Disease

  • Alzheimer Disease Type 1

  • Alzheimers

Neuronal Ceroid Lipofuscinosis
  • Hereditary Ceroid Lipofuscinosis

  • Batten Disease

  • Ncl

  • Neuronal Ceroid-Lipofuscinoses

  • Lipofuscinosis, Ceroid, Neuronal

  • Juvenile Neuronal Ceroid Lipofuscinosis

  • Cerebromacular Dystrophy

  • Cerebromacular Degeneration

  • Ceroid-Lipofuscinosis

  • Ncl - [Neuronal Ceroid Lipofuscinosis]

  • Amaurotic Familial Idiocy

  • Amaurotic Idiocy

  • Amaurotic Idiot

  • Neuronal Lipofuscinosis

  • Pigmentary Retinal Lipoid Neuronal Heredodegeneration

Constipation
Kufor-Rakeb Syndrome
  • Park9

  • Krppd

  • KRS

  • Pallidopyramidal Degeneration With Supranuclear Upgaze Paresis And Dementia

  • Autosomal Recessive Parkinson Disease 9

  • Parkinson Disease 9

  • Parkinson Disease 9, Autosomal Recessive, Juvenile-Onset

  • Autosomal Recessive Juvenile Onset Parkinson Disease 9

  • Parkinson Disease Type 9

  • Pallidopyramidal Degeneration With Supranuclear Upgaze Paresis, And Dementia

  • Park 9

  • Atp13a2-Related Juvenile Neuronal Ceroid Lipofuscinosis

  • Cln12 Disease

  • Juvenile Parkinsonism-Neuronal Ceroid Lipofuscinosis

  • Parkinson Disease Autosomal Recessive 9

Klippel-Feil Syndrome 1, Autosomal Dominant
  • KFS1

  • Cervical Vertebral Fusion Autosomal Dominant

  • Kfs

  • Cervical Vertebral Fusion, Autosomal Dominant

  • Cervical Vertebral Fusion Congenital

  • Congenital Klippel-Feil Segment

  • Fused Cervical Segments Congenital

  • Isolated Klippel-Feil Syndrome

  • Klippel-Feil Malformation

  • Klippel-Feil Sequence

  • Klippel-Feil Syndrome, Type 1, Autosomal Dominant

  • Klippel-Feil Syndrome, Autosomal Dominant

Sleep Disorder
  • Sleep Disorders

  • Non-Organic Sleep Disorder

Meier-Gorlin Syndrome 3
  • MGORS3

  • Meier-Gorlin Syndrome, Type 3

Hereditary Late-Onset Parkinson Disease
  • Autosomal Dominant Late-Onset Parkinson Disease

  • Lopd

  • Hereditary Late Onset Parkinson Disease

Parkinson Disease 15, Autosomal Recessive Early-Onset
  • Parkinsonian-Pyramidal Syndrome

  • Pallidopyramidal Syndrome

  • Parkinson Disease 15, Autosomal Recessive

  • PARK15

  • Pkps

  • Pallido-Pyramidal Syndrome

  • Parkinson'S Disease 15

  • Autosomal Recessive Early-Onset Parkinson Disease 15

  • Autosomal Recessive Early-Onset Parkinson'S Disease 15

  • Pallido-Pyramidal Disease

  • Parkinson Disease 15

  • Parkinson Disease 15 Autosomal Recessive

  • Pps

  • Parkinson Disease, Type 15

Intellectual Developmental Disorder, Autosomal Dominant 55, With Seizures
  • MRD55

  • Mental Retardation, Autosomal Dominant 55, With Seizures

  • Autosomal Dominant Mental Retardation 55

  • Autosomal Dominant Intellectual Developmental Disorder 55

  • Autosomal Dominant Intellectual Developmental Disorder-55 With Seizures

  • Mental Retardation, Autosomal Dominant, Type 55, With Seizures

Hereditary Spastic Paraplegia
  • Familial Spastic Paraplegia

  • Hereditary Spastic Paraparesis

  • Strumpell-Lorrain Disease

  • Hsp

  • Spg

  • Strümpell-Lorrain Disease

  • Spastic Paraplegia, Hereditary

  • French Settlement Disease

  • Strumpell-Lorrain Syndrome

  • Fsp

  • Familial Spastic Paraparesis

  • Spastic Paraplegia, Familial

  • Spastic Paraplegia Hereditary

  • Spastic Paraplegia 3, Autosomal Dominant

  • Spastic Paraparesis

  • Hereditary Spastic Paralysis

  • Familial Spastic Paralysis

  • Hereditary Spastic Ataxia

Rheumatoid Arthritis
  • RA

  • Arthritis, Rheumatoid

  • Rheumatoid Arthritis, Susceptibility To

  • Arthritis Or Polyarthritis, Rheumatic

  • Atrophic Arthritis

  • Rheumatism Arthritis

  • Rheumatoid Polyarthritis

Multiple System Atrophy 1
  • Multiple System Atrophy

  • Shy-Drager Syndrome

  • Msa

  • MSA1

  • Multiple System Atrophy 1, Susceptibility To

  • Sporadic Olivopontocerebellar Atrophy

  • Multisystem Atrophy

  • Msa1, Susceptibility To

  • Multiple System Atrophy, Susceptibility To

  • Opca

  • Progressive Autonomic Failure With Multiple System Atrophy

  • Sds

Parkinson Disease 1, Autosomal Dominant
  • Autosomal Dominant Parkinson Disease 1

  • PARK1

  • Parkinson Disease 1

  • Parkinson'S Disease 1

  • Atypical Parkinson Disease

  • Parkinson Disease 1, Autosomal Dominant Lewy Body

  • Autosomal Dominant Parkinson'S Disease 1

  • Lewy Body Parkinsonism

  • Parkinson Disease Autosomal Dominant 1

  • Parkinson Disease Familial Type 1

  • Parkinson Disease, Type 1

  • Parkinson Disease, Familial, Type 1

Ciliary Dyskinesia, Primary, 43
  • CILD43

  • Primary Ciliary Dyskinesia 43

  • Ciliary Dyskinesia, Primary, 43, With Or Without Situs Inversus

  • Primary Ciliary Dyskinesia 43 With Or Without Situs Inversus

  • Ciliary Dyskinesia, Primary, 43 With Or Without Situs Inversus

Movement Disease
  • Movement Disorders

  • Movement Disorder

Early-Onset Parkinson'S Disease
  • Early-Onset Parkinson Disease

Parkinson Disease 2, Autosomal Recessive Juvenile
  • Young-Onset Parkinson Disease

  • PARK2

  • Pdj

  • Autosomal Recessive Juvenile Parkinson Disease 2

  • Epdf

  • Parkinson Disease, Juvenile, Type 2

  • Parkinson'S Disease 2

  • Autosomal Recessive Juvenile Parkinson Disease

  • Early-Onset Parkinson Disease

  • Parkinson Disease 2

  • Parkinson Disease, Juvenile, Autosomal Recessive

  • Parkinsonism, Early-Onset, With Diurnal Fluctuation

  • Autosomal Recessive Juvenile Parkinson'S Disease 2

  • Jp

  • Juvenile Parkinsonism

  • Parkinson Disease Autosomal Recessive, Early Onset

  • Parkinsonism, Early Onset, With Diurnal Fluctuation

  • Yopd

  • Autosomal Recessive Early-Onset Parkinson Disease Type 2

  • Chromosome 6-Linked Autosomal Recessive Parkinsonism

  • Early-Onset Parkinsonism With Diurnal Fluctuation

  • Parkinsonism Young Adult Onset

  • Parkinson Disease, Type 2

  • Parkinsonism, Juvenile

Vascular Parkinsonism
Dementia, Lewy Body
  • Lewy Body Dementia

  • Lewy Body Disease

  • Diffuse Lewy Body Disease

  • Dementia With Lewy Bodies

  • DLB

  • Autosomal Dominant Diffuse Lewy Body Disease

  • Cortical Lewy Body Disease

  • Dementia, Lewy Body, Susceptibility To

  • Lewy Body Dementia, Susceptibility To

  • Senile Dementia Of The Lewy Body Type

  • Dementia Of The Lewy Body Type

  • Lbd

  • Diffuse Lewy Body Disease With Gaze Palsy

  • Dysphasic Dementia Hereditary

  • Lewy Body Type Senile Dementia

  • Lewy Body Variant Of Alzheimer Disease

  • Lewy Bodies

  • Lewy Body

  • Dlbd - [Diffuse Lewy Body Disease]

  • Clbd - [Cortical Lewy Body Disease]

3-Methylglutaconic Aciduria, Type Iii
  • Optic Atrophy

  • 3-Methylglutaconic Aciduria Type 3

  • Costeff Syndrome

  • Mga3

  • Costeff Optic Atrophy Syndrome

  • Optic Atrophy Plus Syndrome

  • Infantile Optic Atrophy With Chorea And Spastic Paraplegia

  • 3-Methylglutaconic Aciduria Type Iii

  • Autosomal Recessive Optic Atrophy Plus Syndrome

  • Autosomal Recessive Optic Atrophy Type 3

  • Opa3 Defect

  • MGCA3

  • Mga, Type Iii

  • Iraqi Jewish Optic Atrophy Plus

  • Mga Type Iii

  • Optic Atrophy, Infantile, With Chorea And Spastic Paraplegia

  • Iraqi-Jewish 'Optic Atrophy Plus'

  • Optic Atrophy 3, Autosomal Recessive

  • Opa3, Autosomal Recessive

  • Opa3-Related 3-Methylglutaconic Aciduria

  • Iraqi-Jewish Optic Atrophy Plus

  • Atrophy Of Optic Disc

  • 3-Alpha Methylglutaconic Aciduria Type Iii

  • Optic Atrophy 3

  • Optic Atrophy Infantile With Chorea And Spastic Paraplegia

  • Autosomal Recessive Opa3

  • Autosomal Recessive Optic Atrophy 3

  • 3-Methylglutaconic Aciduria 3

  • 3-Alpha-Methylglutaconic Aciduria Type 3

  • Optic Atrophy 3 Autosomal Recessive

  • Atrophy, Optic

  • Atrophy, Optic, Plus Syndrome

  • Optic Nerve Atrophy

  • Primary Optic Atrophy

  • Oa - [Optic Atrophy]

  • Second Cranial Nerve Atrophy

  • Second Cranium Nerve Atrophy

Parkinson Disease, Late-Onset
  • Parkinson Disease

  • Parkinson'S Disease

  • PD

  • PARK

  • Parkinson Disease, Susceptibility To

  • Late Onset Parkinson'S Disease

  • Late Onset Parkinson Disease

  • Paralysis Agitans

  • Primary Parkinsonism

  • Idiopathic Parkinson Disease

  • Parkinson'S

  • Parkinson Disease, Late-Onset, Susceptibility To

  • Parkinson Disease, Age Of Onset, Modifier

  • Lewy Body Parkinson Disease

  • Idiopathic Parkinson'S Disease

  • Pd - [Parkinson Disease]

  • Parkinson Disease Nos

  • Parkinson, Nos

  • Primary Parkinson Disease

Parkinson Disease 3, Autosomal Dominant
  • Parkinson Disease 3

  • PARK3

  • Parkinson Disease 3, Autosomal Dominant Lewy Body

  • Parkinson'S Disease 3

  • Autosomal Dominant Lewy Body Parkinson Disease 3

  • Autosomal Dominant Parkinson Disease 3

  • Parkinson Disease Type 3

  • Autosomal Dominant Parkinson Disease

  • Parkinson Disease, Autosomal Dominant

  • Parkinson Disease, Familial, Type 1

Choreatic Disease
  • Chorea

  • Hereditary Chorea

Amyotrophic Lateral Sclerosis-Parkinsonism/Dementia Complex 1
  • Guam Disease

  • Amyotrophic Lateral Sclerosis-Parkinsonism/Dementia Complex Of Guam

  • Als-Pdc

  • Lytico-Bodig Disease

  • Amyotrophic Lateral Sclerosis-Parkinsonism-Dementia Complex

  • Amyotrophic Lateral Sclerosis-Parkinsonism/Dementia Complex 1, Susceptibility To

  • Amyotrophic Lateral Sclerosis-Parkinsonism/Dementia Complex, Susceptibility To

  • Amyotrophic Lateral Sclerosis-Parkinsonism/Dementia Complex

  • Amyotrophic Lateral Sclerosis-Parkinsonism-Dementia Of Guam Syndrome

  • Parkinsonism-Dementia-Als Complex

  • Pdals

  • Amyotrophic Lateral Sclerosis, Parkinsonism/Dementia Complex Of Guam

  • Parkinson-Dementia Complex Of Guam

  • G-Pdc

  • Guam Parkinsonism-Dementia Complex

  • ALS-PDC1

  • Als/Pdc Of Guam

  • Amyotrophic Lateral Sclerosis

  • Sclerosis, Lateral, Amyotrophic/Parkinsonism/Dementia Complex 1

  • Amyotrophic Lateral Sclerosis, Guam Form

  • Parkinsonian Disorders

Parkinson Disease 8, Autosomal Dominant
  • Parkinson Disease 8

  • Autosomal Dominant Parkinson Disease 8

  • PARK8

  • Parkinson'S Disease 8

  • Autosomal Dominant Parkinson'S Disease 8

  • Parkinson Disease-8

  • Parkinson Disease, Type 8, Autosomal Dominant

Pick Disease Of Brain
  • Pick Disease

  • Pick Disease Of The Brain

  • Lobar Atrophy Of Brain

  • Dementia With Lobar Atrophy And Neuronal Cytoplasmic Inclusions

  • Pick'S Disease

  • Behavioral Variant Of Frontotemporal Dementia

  • Dementia In Pick'S Disease

  • Lobar Atrophy Of The Brain

  • Bvftd

  • Bv-Ftd

  • PIDB

  • Picks Disease

Parkinsonism
  • Parkinsonism-Plus

  • Idiopathic Parkinsonism

  • Primary Parkinsonism

  • Paralysis Agitans Syndrome

  • Parkinsonian Syndrome

  • Trembling Paralysis

  • Paralysis Agitans

  • Shaking Palsy

  • Shaking Paralysis

Cerebellar Disease
  • Cerebellar Diseases

  • Cerebellar Dysfunction

  • Cerebellar Abnormality

  • Cerebellar Disorders

Gerstmann-Straussler Disease
  • Gerstmann-Straussler-Scheinker Disease

  • Gerstmann-Straussler-Scheinker Syndrome

  • Prion Dementia

  • Cerebral Amyloid Angiopathy, Prnp-Related

  • GSD

  • Gss

  • Cerebellar Ataxia, Progressive Dementia, And Amyloid Deposits In Cns

  • Amyloidosis, Cerebral, With Spongiform Encephalopathy

  • Subacute Spongiform Encephalopathy, Gerstmann-Straussler Type

  • Encephalopathy, Subacute Spongiform, Gerstmann-Straussler Type

  • Amyloidosis Cerebral With Spongiform Encephalopathy

  • Cerebellar Ataxia, Progressive Dementia, And Amyloid Deposits In The Central Nervous System

  • Encephalopathy Subacute Spongiform Gerstmann-Straussler Type

  • Gssd

  • Gerstmann Straussler Scheinker Syndrome

  • Cerebral Amyloidosis With Spongiform Encephalopathy

  • Subacute Spongiform Encephalopathy Gerstmann-Straussler Type

  • Gluthathione Synthetase Deficiency

  • Gerstmann Straussler Syndrome

Creutzfeldt-Jakob Disease
  • Variant Creutzfeldt-Jakob Disease

  • CJD

  • Bovine Spongiform Encephalopathy

  • Vcjd

  • Inherited Creutzfeldt-Jakob Disease

  • Creutzfeldt-Jakob Disease, Familial

  • Creutzfeldt Jakob Disease

  • Creutzfeldt-Jacob Disease

  • Creutzfeldt Jacob Disease

  • Sporadic Creutzfeldt-Jakob Disease

  • Encephalopathy, Bovine Spongiform

  • Creutzfeldt-Jakob Disease, Variant, Resistance To

  • Creutzfeldt-Jakob Disease, Variant

  • Creutzfeldt Jacob Syndrome

  • Jakob-Creutzfeldt Disease

  • Subacute Spongiform Encephalopathy

  • Transmissible Virus Dementia

  • New Variant Of Cjd

  • Nv-Cjd

  • Variant Cjd

  • Variant Creutzfeldt-Jacob Disease

  • Sporadic Cjd

  • Inherited Cjd

  • Acquired Creutzfeldt-Jakob Disease

  • Variant Mcj

  • Encephalopathy Bovine Spongiform

  • Familial Creutzfeldt-Jakob Disease

  • Creutzfeldt-Jakob Syndrome

  • New Variant Creutzfeldt-Jakob Disease

  • Creutzfeldt-Jakob Disease, Sporadic

  • Acquired Cjd

  • Scjd - [Sporadic Creutzfeldt-Jakob Disease]

  • Idiopathic Creutzfeldt-Jakob Disease

  • Creutzfeld-Jakob Disease Nos

  • Vcjd - [Variant Creutzfeldt-Jakob Disease]

Gaucher'S Disease
  • Gaucher Disease

  • Kerasin Thesaurismosis

  • Glucocerebrosidase Deficiency

  • Glucosylceramidase Deficiency

  • Acid Beta-Glucosidase Deficiency

  • Glucosylceramide Beta-Glucosidase Deficiency

  • Acute Cerebral Gaucher Disease

  • Cerebroside Lipidosis Syndrome

  • Gaucher Splenomegaly

  • Glucocerebrosidosis

  • Glucosyl Cerebroside Lipidosis

  • Kerasin Lipoidosis

  • Lipoid Histiocytosis

  • Glocucerebrosidase Deficiency

  • Sphingolipidosis 1

  • Gaucher Syndrome

  • Gauchers Disease

  • Gd

  • Glucosylceramide Lipidosis

  • Kerasin Histiocytosis

  • Gaucher Disease, Type 1

  • Gaucher Disease, Type 2

Tremor
  • Medicament-Induced Tremor

  • Medication-Induced Postural Tremor

Mitochondrial Complex I Deficiency, Nuclear Type 1
  • Mitochondrial Complex I Deficiency

  • Nadh:Q(1) Oxidoreductase Deficiency

  • MC1DN1

  • Nadh-Coenzyme Q Reductase Deficiency

  • Isolated Mitochondrial Respiratory Chain Complex I Deficiency

  • Isolated Nadh-Coenzyme Q Reductase Deficiency

  • Isolated Nadh-Coq Reductase Deficiency

  • Isolated Nadh-Ubiquinone Reductase Deficiency

  • Mitochondrial Nadh Dehydrogenase Component Of Complex I, Deficiency Of

  • Nuclear Type Mitochondrial Complex I Deficiency 1

  • Isolated Complex I Deficiency

  • Complex 1 Mitochondrial Respiratory Chain Deficiency

  • Nadh Coenzyme Q Reductase Deficiency

  • Complex I Mitochondrial Respiratory Chain Deficiency

  • Deficiency Of Mitochondrial Nadh Dehydrogenase Component Of Complex I

  • Nadh:Ubiquinone Oxidoreductase Deficiency

  • Complex I, Mitochondrial Respiratory Chain, Deficiency Of

Autosomal Dominant Cerebellar Ataxia
  • Spinocerebellar Ataxia

  • Adca

  • Pierre Marie Cerebellar Ataxia

  • Ataxia, Spinocerebellar

  • Sca

  • Autosomal Dominant Spinocerebellar Ataxia

  • Spinocerebellar Ataxias

Von Economo'S Disease
  • Encephalitis Lethargica

  • Von Economo Encephalitis

  • Von Economo Disease

Supranuclear Palsy, Progressive, 1
  • Progressive Supranuclear Palsy

  • Steele-Richardson-Olszewski Syndrome

  • Supranuclear Palsy, Progressive

  • Psp

  • Progressive Supranuclear Ophthalmoplegia

  • PSNP1

  • Familial Progressive Supranuclear Palsy

  • Richardson'S Syndrome

  • Psp Syndrome

  • Progressive Supranuclear Palsy 1

  • Supranuclear Palsy Progressive

  • Ophthalmoplegia, Supranuclear, Progressive

  • Steele-Richardson-Olszewksi Syndrome

Essential Tremor
  • Benign Essential Tremor

  • Familial Tremor

  • Hereditary Essential Tremor

  • Essential Hereditary Tremor

  • Shaky Hand Syndrome

  • Benign Essential Tremor Syndrome

  • Tremor Hereditary Essential

  • Essential Tremor, Susceptibility To

  • Tremor, Hereditary Essential

Gaucher Disease, Type I
  • Glucocerebrosidase Deficiency

  • Acid Beta-Glucosidase Deficiency

  • Gba Deficiency

  • GD1

  • Gd I

  • Gaucher Disease, Noncerebral Juvenile

  • Gaucher Disease Type 1

  • Gaucher Disease Type I

  • Gaucher'S Disease Type I

  • Gaucher Disease

  • Gd 1

  • Non-Cerebral Juvenile Gaucher Disease

  • GD

  • Gaucher Disease 1

  • Adult Non-Neuronopathic Gaucher Disease

  • Noncerebral Juvenile Gaucher Disease

  • Type 1 Gaucher Disease

  • Gaucher Disease, Type 1

Amyotrophic Lateral Sclerosis 1
  • Amyotrophic Lateral Sclerosis

  • ALS

  • Lou Gehrig Disease

  • Amyotrophic Lateral Sclerosis Type 1

  • Charcot Disease

  • ALS1

  • Amyotrophic Lateral Sclerosis, Susceptibility To

  • Fals

  • Lou Gehrig'S Disease

  • Mnd

  • Motor Neuron Disease

  • Familial Amyotrophic Lateral Sclerosis

  • Amyotrophic Lateral Sclerosis 1, Familial

  • Amyotrophic Lateral Sclerosis 1, Autosomal Dominant

  • Motor Neuron Disease, Bulbar

  • Motor Neurone Disease

  • Amyotrophic Lateral Sclerosis With Dementia

  • Dementia With Amyotrophic Lateral Sclerosis

  • Motor Neuron Disease, Amyotrophic Lateral Sclerosis

  • Sclerosis, Lateral, Amyotrophic

  • Sclerosis, Lateral, Amyotrophic, Type 1

  • Amyotrophic Sclerosis

  • Als - [Amyotrophic Lateral Sclerosis]

  • Wasting Palsy

  • Amyotrophic Paralysis

  • Amyotrophy Lateral Sclerosis

  • Wasting Paralysis

  • Spinal Progressive Amyotrophy

  • Progressive Atrophic Paralysis

Striatonigral Degeneration
Toxic Encephalopathy
  • Neurotoxicity

  • Neurotoxicity Syndromes

  • Neurotoxicity Syndrome

  • Encephalopathy, Toxic

Leprosy 3
  • Leprosy

  • Leprosy, Susceptibility To, 3

  • Hansen'S Disease

  • Leprosy, Susceptibility To

  • Hansen Disease

  • Infection Due To Mycobacterium Leprae

  • LPRS3

  • Leprosy, Type 3

  • Anaesthesia Leprosy

  • Anaesthetic Leprosy

  • Maculoanaesthetic Leprosy

  • Macular Leprosy

  • Leprosy Unspecified

Sphingolipidosis
  • Sphingolipidoses

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Felis catus LRRK2 VGNC VGNC:97488
Rattus norvegicus LRRK2 RGD RGD:1561168
Bos taurus LRRK2 VGNC VGNC:31038
Mus musculus LRRK2 MGD MGI:1913975
Canis familiaris LRRK2 VGNC VGNC:42823
Macaca mulatta LRRK2 VGNC VGNC:81447
Others LRRK2 NCBI