SPG21 - SPG21 abhydrolase domain containing, maspardin Gene

Also Known as MAST; ACP33; GL010; ABHD21; BM-019

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 51324

About SPG21

Cytogenetic location: 15q22.31 Genomic coordinates (GRCh38): 15:64,963,022-64,989,914 (from NCBI)

This gene has 14 transcripts (splice variants), 222 orthologues and is associated with 2 phenotypes. Ubiquitous expression in thyroid (RPKM 30.9), placenta (RPKM 23.1) and 25 other tissues.

Summary

The protein encoded by this gene binds to the hydrophobic C-terminal Amino acids of CD4 which are involved in repression of T cell activation. The interaction with CD4 is mediated by the noncatalytic alpha/beta hydrolase fold domain of this protein. It is thus proposed that this gene product modulates the stimulatory activity of CD4. Mutations in this gene are associated with autosomal recessive spastic paraplegia 21 (SPG21), also known as mast syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2014]

SPG21 Products (3)

mRNA Protein Name
NM_001127889.5 NP_001121361.1 maspardin isoform a
NM_001127890.5 NP_001121362.1 maspardin isoform b
NM_016630.7 NP_057714.1 maspardin isoform a
Molecular Function GO Annotation Evidence References Source
enables CD4 receptor binding IPI
IPI: Inferred from physical interaction
11113139 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
16189514 GOA
Cellular Component GO Annotation Evidence References Source
located in cytosol IDA
IDA: Inferred from direct assay
11113139 GOA
located in trans-Golgi network transport vesicle IDA
IDA: Inferred from direct assay
11113139 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

SPG21 Protein Structure

Abhydrolase_6

Abhydrolase_6: Alpha/beta hydrolase family (46 - 264)

  • 0
  • 100
  • 200
  • 308 a.a.
Protein Preferred Names Protein Names

maspardin

  • SPG21, maspardin

SPG21 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
SPG21 Q9NZD8 CCDC102B Homo sapiens Q68D86 25416956
Intra
SPG21 Q9NZD8 PNMA5 Homo sapiens Q96PV4 32296183
Intra
SPG21 Q9NZD8 PNMA5 Homo sapiens Q96PV4 32296183
Intra
SPG21 Q9NZD8 MID2 Homo sapiens Q9UJV3-2 32296183
Intra
SPG21 Q9NZD8 MID2 Homo sapiens Q9UJV3-2 32296183
Intra
SPG21 Q9NZD8 MID2 Homo sapiens Q9UJV3-2 32296183
Intra
SPG21 Q9NZD8 CCHCR1 Homo sapiens Q8TD31-3 32296183
Intra
SPG21 Q9NZD8 CCHCR1 Homo sapiens Q8TD31-3 32296183
Intra
SPG21 Q9NZD8 BORCS6 Homo sapiens Q96GS4 32296183
Intra
SPG21 Q9NZD8 BORCS6 Homo sapiens Q96GS4 32296183
Intra
SPG21 Q9NZD8 RTL8B Homo sapiens Q17RB0 32296183
Intra
SPG21 Q9NZD8 RTL8B Homo sapiens Q17RB0 32296183
Intra
SPG21 Q9NZD8 TSGA10IP Homo sapiens Q3SY00 32296183
Intra
SPG21 Q9NZD8 TSGA10IP Homo sapiens Q3SY00 32296183
Intra
SPG21 Q9NZD8 LSMEM2 Homo sapiens Q8N112 32296183
Intra
SPG21 Q9NZD8 LSMEM2 Homo sapiens Q8N112 32296183
Intra
SPG21 Q9NZD8 MAB21L3 Homo sapiens Q8N8X9 32296183
Intra
SPG21 Q9NZD8 MAB21L3 Homo sapiens Q8N8X9 32296183
Intra
SPG21 Q9NZD8 SPMIP6 Homo sapiens Q8NCR6 32296183
Intra
SPG21 Q9NZD8 SPMIP6 Homo sapiens Q8NCR6 32296183
Intra
SPG21 Q9NZD8 PBX4 Homo sapiens Q9BYU1 32296183
Intra
SPG21 Q9NZD8 PBX4 Homo sapiens Q9BYU1 32296183
Intra
SPG21 Q9NZD8 TXNL4B Homo sapiens Q9NX01 32296183
Intra
SPG21 Q9NZD8 TXNL4B Homo sapiens Q9NX01 32296183
Intra
SPG21 Q9NZD8 NRDE2 Homo sapiens Q9H7Z3 32296183
Intra
SPG21 Q9NZD8 NRDE2 Homo sapiens Q9H7Z3 32296183
Intra
SPG21 Q9NZD8 GRPEL1 Homo sapiens Q9HAV7 32296183
Intra
SPG21 Q9NZD8 GRPEL1 Homo sapiens Q9HAV7 32296183
Intra
SPG21 Q9NZD8 ACOT13 Homo sapiens Q9NPJ3 32296183
Intra
SPG21 Q9NZD8 ACOT13 Homo sapiens Q9NPJ3 32296183
Intra
SPG21 Q9NZD8 CDK2AP1 Homo sapiens O14519 32296183
Intra
SPG21 Q9NZD8 CDK2AP1 Homo sapiens O14519 32296183
Intra
SPG21 Q9NZD8 GAS8 Homo sapiens O95995 32296183
Intra
SPG21 Q9NZD8 GAS8 Homo sapiens O95995 32296183
Intra
SPG21 Q9NZD8 CMTM6 Homo sapiens Q9NX76 32296183
Intra
SPG21 Q9NZD8 CMTM6 Homo sapiens Q9NX76 32296183
Intra
SPG21 Q9NZD8 REL Homo sapiens Q04864-2 32296183
Intra
SPG21 Q9NZD8 REL Homo sapiens Q04864-2 32296183
Intra
SPG21 Q9NZD8 TFIP11 Homo sapiens Q9UBB9 32296183
Intra
SPG21 Q9NZD8 TFIP11 Homo sapiens Q9UBB9 32296183
Intra
SPG21 Q9NZD8 TFIP11 Homo sapiens Q9UBB9 32296183
Intra
SPG21 Q9NZD8 SYNGR3 Homo sapiens O43761 32296183
Intra
SPG21 Q9NZD8 SYNGR3 Homo sapiens O43761 32296183
Intra
SPG21 Q9NZD8 MTUS2 Homo sapiens Q5JR59-3 32296183
Intra
SPG21 Q9NZD8 MTUS2 Homo sapiens Q5JR59-3 32296183
Intra
SPG21 Q9NZD8 AGTRAP Homo sapiens Q6RW13-2 32296183
Intra
SPG21 Q9NZD8 AGTRAP Homo sapiens Q6RW13-2 32296183
Intra
SPG21 Q9NZD8 CMTM5 Homo sapiens Q96DZ9-2 32296183
Intra
SPG21 Q9NZD8 CMTM5 Homo sapiens Q96DZ9-2 32296183
Intra
SPG21 Q9NZD8 CPSF7 Homo sapiens Q8N684-3 32296183
Intra
SPG21 Q9NZD8 CPSF7 Homo sapiens Q8N684-3 32296183
Intra
SPG21 Q9NZD8 TMEM239 Homo sapiens Q8WW34-2 32296183
Intra
SPG21 Q9NZD8 TMEM239 Homo sapiens Q8WW34-2 32296183
Intra
SPG21 Q9NZD8 FLACC1 Homo sapiens Q96Q35-2 32296183
Intra
SPG21 Q9NZD8 FLACC1 Homo sapiens Q96Q35-2 32296183
Intra
SPG21 Q9NZD8 ATPAF2 Homo sapiens Q8N5M1 32296183
Intra
SPG21 Q9NZD8 ATPAF2 Homo sapiens Q8N5M1 25416956
Intra
SPG21 Q9NZD8 ATPAF2 Homo sapiens Q8N5M1 25416956
Intra
SPG21 Q9NZD8 ATPAF2 Homo sapiens Q8N5M1 32296183
Intra
SPG21 Q9NZD8 TLE5 Homo sapiens Q08117-2 32296183
Intra
SPG21 Q9NZD8 TLE5 Homo sapiens Q08117-2 32296183
Intra
SPG21 Q9NZD8 CFAP410 Homo sapiens O43822-4 32296183
Intra
SPG21 Q9NZD8 CFAP410 Homo sapiens O43822-4 32296183
Intra
SPG21 Q9NZD8 IQCB1 Homo sapiens Q15051-2 32296183
Intra
SPG21 Q9NZD8 IQCB1 Homo sapiens Q15051-2 32296183
Intra
SPG21 Q9NZD8 DRC12 Homo sapiens Q494R4-2 32296183
Intra
SPG21 Q9NZD8 DRC12 Homo sapiens Q494R4-2 32296183
Intra
SPG21 Q9NZD8 ZMYND12 Homo sapiens Q9H0C1 32296183
Intra
SPG21 Q9NZD8 ZMYND12 Homo sapiens Q9H0C1 32296183
Intra
SPG21 Q9NZD8 UFSP1 Homo sapiens Q6NVU6 32296183
Intra
SPG21 Q9NZD8 UFSP1 Homo sapiens Q6NVU6 32296183
Intra
SPG21 Q9NZD8 TPD52 Homo sapiens P55327-2 32296183
Intra
SPG21 Q9NZD8 TPD52 Homo sapiens P55327-2 32296183
Intra
SPG21 Q9NZD8 CTIF Homo sapiens O43310-2 32296183
Intra
SPG21 Q9NZD8 CTIF Homo sapiens O43310-2 32296183
Intra
SPG21 Q9NZD8 SYNGR1 Homo sapiens O43759-2 32296183
Intra
SPG21 Q9NZD8 SYNGR1 Homo sapiens O43759-2 32296183
Intra
SPG21 Q9NZD8 APOC1 Homo sapiens P02654 32296183
Intra
SPG21 Q9NZD8 APOC1 Homo sapiens P02654 32296183
Intra
SPG21 Q9NZD8 EIF4H Homo sapiens Q15056-2 32296183
Intra
SPG21 Q9NZD8 EIF4H Homo sapiens Q15056-2 32296183
Intra
SPG21 Q9NZD8 KRT13 Homo sapiens P13646 32296183
Intra
SPG21 Q9NZD8 KRT13 Homo sapiens P13646 32296183
Intra
SPG21 Q9NZD8 ZBTB42 Homo sapiens B2RXF5 32296183
Intra
SPG21 Q9NZD8 ZBTB42 Homo sapiens B2RXF5 32296183
Intra
SPG21 Q9NZD8 CEPT1 Homo sapiens Q9Y6K0 32296183
Intra
SPG21 Q9NZD8 CEPT1 Homo sapiens Q9Y6K0 32296183
Intra
SPG21 Q9NZD8 CEPT1 Homo sapiens Q9Y6K0 32296183
Intra
SPG21 Q9NZD8 EYA2 Homo sapiens O00167-2 32296183
Intra
SPG21 Q9NZD8 EYA2 Homo sapiens O00167-2 32296183
Intra
SPG21 Q9NZD8 TOX2 Homo sapiens Q96NM4-3 32296183
Intra
SPG21 Q9NZD8 TOX2 Homo sapiens Q96NM4-3 32296183
Intra
SPG21 Q9NZD8 SPMIP5 Homo sapiens Q8WW14-2 32296183
Intra
SPG21 Q9NZD8 SPMIP5 Homo sapiens Q8WW14-2 32296183
Intra
SPG21 Q9NZD8 FAM86C1P Homo sapiens Q9NVL1-2 32296183
Intra
SPG21 Q9NZD8 FAM86C1P Homo sapiens Q9NVL1-2 32296183
Intra
SPG21 Q9NZD8 TMEM208 Homo sapiens Q9BTX3 32296183
Intra
SPG21 Q9NZD8 TMEM208 Homo sapiens Q9BTX3 32296183
Intra
SPG21 Q9NZD8 PPM1J Homo sapiens Q5JR12 32296183
Intra
SPG21 Q9NZD8 PPM1J Homo sapiens Q5JR12 32296183
Intra
SPG21 Q9NZD8 SLC35E3 Homo sapiens Q7Z769 32296183
Intra
SPG21 Q9NZD8 SLC35E3 Homo sapiens Q7Z769 32296183
Intra
SPG21 Q9NZD8 ROPN1 Homo sapiens Q9HAT0 32296183
Intra
SPG21 Q9NZD8 ROPN1 Homo sapiens Q9HAT0 32296183
Intra
SPG21 Q9NZD8 REEP6 Homo sapiens Q96HR9-2 32296183
Intra
SPG21 Q9NZD8 REEP6 Homo sapiens Q96HR9-2 32296183
Intra
SPG21 Q9NZD8 RAD51C Homo sapiens O43502-2 32296183
Intra
SPG21 Q9NZD8 RAD51C Homo sapiens O43502-2 32296183
Intra
SPG21 Q9NZD8 CMTM4 Homo sapiens Q8IZR5-2 32296183
Intra
SPG21 Q9NZD8 CMTM4 Homo sapiens Q8IZR5-2 32296183
Intra
SPG21 Q9NZD8 SRGAP2B Homo sapiens A0A286YEY3 32296183
Intra
SPG21 Q9NZD8 SRGAP2B Homo sapiens A0A286YEY3 32296183
Intra
SPG21 Q9NZD8 CLDN22 Homo sapiens Q8N7P3 32296183
Intra
SPG21 Q9NZD8 CLDN22 Homo sapiens Q8N7P3 32296183
Intra
SPG21 Q9NZD8 HSD17B13 Homo sapiens Q7Z5P4 32296183
Intra
SPG21 Q9NZD8 HSD17B13 Homo sapiens Q7Z5P4 32296183
Intra
SPG21 Q9NZD8 TRIM54 Homo sapiens Q9BYV2 32296183
Intra
SPG21 Q9NZD8 TRIM54 Homo sapiens Q9BYV2 25416956
Intra
SPG21 Q9NZD8 TRIM54 Homo sapiens Q9BYV2 32296183
Intra
SPG21 Q9NZD8 TRIM54 Homo sapiens Q9BYV2 25416956
Intra
SPG21 Q9NZD8 ATP5ME Homo sapiens P56385 32296183
Intra
SPG21 Q9NZD8 ATP5ME Homo sapiens P56385 32296183
Intra
SPG21 Q9NZD8 DTX3L Homo sapiens Q8TDB6 25416956
Intra
SPG21 Q9NZD8 DTX3L Homo sapiens Q8TDB6 25416956
Intra
SPG21 Q9NZD8 EFHC2 Homo sapiens Q5JST6 32296183
Intra
SPG21 Q9NZD8 EFHC2 Homo sapiens Q5JST6 25416956
Intra
SPG21 Q9NZD8 EFHC2 Homo sapiens Q5JST6 25416956
Intra
SPG21 Q9NZD8 EFHC2 Homo sapiens Q5JST6 32296183
Intra
SPG21 Q9NZD8 N4BP3 Homo sapiens O15049 32296183
Intra
SPG21 Q9NZD8 N4BP3 Homo sapiens O15049 32296183
Intra
SPG21 Q9NZD8 CMTM5 Homo sapiens Q96DZ9 25416956
Intra
SPG21 Q9NZD8 CMTM5 Homo sapiens Q96DZ9 25416956
Intra
SPG21 Q9NZD8 NDUFAF2 Homo sapiens Q8N183 32296183
Intra
SPG21 Q9NZD8 NDUFAF2 Homo sapiens Q8N183 32296183
Intra
SPG21 Q9NZD8 FAM114A1 Homo sapiens Q8IWE2 31515488
Intra
SPG21 Q9NZD8 FAM114A1 Homo sapiens Q8IWE2 25416956
Intra
SPG21 Q9NZD8 FAM114A1 Homo sapiens Q8IWE2 32296183
Intra
SPG21 Q9NZD8 FAM114A1 Homo sapiens Q8IWE2 25416956
Intra
SPG21 Q9NZD8 FAM114A1 Homo sapiens Q8IWE2 32296183
Intra
SPG21 Q9NZD8 VMAC Homo sapiens Q2NL98 32296183
Intra
SPG21 Q9NZD8 VMAC Homo sapiens Q2NL98 32296183
Intra
SPG21 Q9NZD8 NR1D1 Homo sapiens P20393 32296183
Intra
SPG21 Q9NZD8 NR1D1 Homo sapiens P20393 32296183
Intra
SPG21 Q9NZD8 TRIM14 Homo sapiens Q14142 32296183
Intra
SPG21 Q9NZD8 TRIM14 Homo sapiens Q14142 32296183
Intra
SPG21 Q9NZD8 SFT2D1 Homo sapiens Q8WV19 32296183
Intra
SPG21 Q9NZD8 SFT2D1 Homo sapiens Q8WV19 32296183
Intra
SPG21 Q9NZD8 HNRNPH1 Homo sapiens P31943 32296183
Intra
SPG21 Q9NZD8 HNRNPH1 Homo sapiens P31943 32296183
Intra
SPG21 Q9NZD8 TRAF2 Homo sapiens Q12933 32296183
Intra
SPG21 Q9NZD8 TRAF2 Homo sapiens Q12933 25416956
Intra
SPG21 Q9NZD8 TRAF2 Homo sapiens Q12933 32296183
Intra
SPG21 Q9NZD8 TRAF2 Homo sapiens Q12933 25416956
Intra
SPG21 Q9NZD8 GEMIN4 Homo sapiens P57678 32296183
Intra
SPG21 Q9NZD8 GEMIN4 Homo sapiens P57678 32296183
Intra
SPG21 Q9NZD8 TFG Homo sapiens Q92734 32296183
Intra
SPG21 Q9NZD8 TFG Homo sapiens Q92734 32296183
Intra
SPG21 Q9NZD8 TFG Homo sapiens Q92734 25416956
Intra
SPG21 Q9NZD8 TFG Homo sapiens Q92734 32296183
Intra
SPG21 Q9NZD8 PFDN5 Homo sapiens Q99471 32296183
Intra
SPG21 Q9NZD8 PFDN5 Homo sapiens Q99471 32296183
Intra
SPG21 Q9NZD8 PCNA Homo sapiens P12004 32296183
Intra
SPG21 Q9NZD8 PCNA Homo sapiens P12004 32296183
Intra
SPG21 Q9NZD8 TRAF1 Homo sapiens Q13077 32296183
Intra
SPG21 Q9NZD8 TRAF1 Homo sapiens Q13077 25416956
Intra
SPG21 Q9NZD8 TRAF1 Homo sapiens Q13077 32296183
Intra
SPG21 Q9NZD8 ARMC12 Homo sapiens Q5T9G4-2 32296183
Intra
SPG21 Q9NZD8 ARMC12 Homo sapiens Q5T9G4-2 32296183
Intra
SPG21 Q9NZD8 SEPTIN5 Homo sapiens Q99719 32296183
Intra
SPG21 Q9NZD8 SEPTIN5 Homo sapiens Q99719 32296183
Intra
SPG21 Q9NZD8 COG6 Homo sapiens Q9Y2V7 32296183
Intra
SPG21 Q9NZD8 COG6 Homo sapiens Q9Y2V7 32296183
Intra
SPG21 Q9NZD8 COG6 Homo sapiens Q9Y2V7 32296183
Intra
SPG21 Q9NZD8 MYOG Homo sapiens P15173 32296183
Intra
SPG21 Q9NZD8 MYOG Homo sapiens P15173 32296183
Intra
SPG21 Q9NZD8 KCTD9 Homo sapiens Q7L273 32296183
Intra
SPG21 Q9NZD8 KCTD9 Homo sapiens Q7L273 32296183
Intra
SPG21 Q9NZD8 ARL8A Homo sapiens Q96BM9 32296183
Intra
SPG21 Q9NZD8 ARL8A Homo sapiens Q96BM9 32296183
Intra
SPG21 Q9NZD8 GOLT1B Homo sapiens Q9Y3E0 32296183
Intra
SPG21 Q9NZD8 GOLT1B Homo sapiens Q9Y3E0 32296183
Intra
SPG21 Q9NZD8 GOLT1B Homo sapiens Q9Y3E0 32296183
Intra
SPG21 Q9NZD8 GEMIN2 Homo sapiens O14893 32296183
Intra
SPG21 Q9NZD8 GEMIN2 Homo sapiens O14893 32296183
Intra
SPG21 Q9NZD8 GGA2 Homo sapiens Q9UJY4 32296183
Intra
SPG21 Q9NZD8 GGA2 Homo sapiens Q9UJY4 32296183
Intra
SPG21 Q9NZD8 GGA2 Homo sapiens Q9UJY4 32296183
Intra
SPG21 Q9NZD8 S100B Homo sapiens P04271 25416956
Intra
SPG21 Q9NZD8 S100B Homo sapiens P04271 32296183
Intra
SPG21 Q9NZD8 S100B Homo sapiens P04271 25416956
Intra
SPG21 Q9NZD8 S100B Homo sapiens P04271 32296183
Intra
SPG21 Q9NZD8 TRIB3 Homo sapiens Q96RU7 32296183
Intra
SPG21 Q9NZD8 TRIB3 Homo sapiens Q96RU7 32296183
Intra
SPG21 Q9NZD8 SPRED1 Homo sapiens Q7Z699 32296183
Intra
SPG21 Q9NZD8 SPRED1 Homo sapiens Q7Z699 32296183
Intra
SPG21 Q9NZD8 SWSAP1 Homo sapiens Q6NVH7 32296183
Intra
SPG21 Q9NZD8 SWSAP1 Homo sapiens Q6NVH7 32296183
Intra
SPG21 Q9NZD8 TCF4 Homo sapiens P15884 25416956
Intra
SPG21 Q9NZD8 TXN Homo sapiens P10599 32296183
Intra
SPG21 Q9NZD8 TXN Homo sapiens P10599 32296183
Intra
SPG21 Q9NZD8 PSMB4 Homo sapiens P28070 32296183
Intra
SPG21 Q9NZD8 PSMB4 Homo sapiens P28070 32296183
Intra
SPG21 Q9NZD8 PLP2 Homo sapiens Q04941 32296183
Intra
SPG21 Q9NZD8 PLP2 Homo sapiens Q04941 32296183
Intra
SPG21 Q9NZD8 GOLGA2 Homo sapiens Q08379 32296183
Intra
SPG21 Q9NZD8 GOLGA2 Homo sapiens Q08379 32296183
Intra
SPG21 Q9NZD8 PCBD2 Homo sapiens Q9H0N5 32296183
Intra
SPG21 Q9NZD8 PCBD2 Homo sapiens Q9H0N5 32296183
Intra
SPG21 Q9NZD8 INCA1 Homo sapiens Q0VD86 32296183
Intra
SPG21 Q9NZD8 INCA1 Homo sapiens Q0VD86 25416956
Intra
SPG21 Q9NZD8 INCA1 Homo sapiens Q0VD86 32296183
Intra
SPG21 Q9NZD8 TSNAXIP1 Homo sapiens Q2TAA8 32296183
Intra
SPG21 Q9NZD8 TSNAXIP1 Homo sapiens Q2TAA8 32296183
Intra
SPG21 Q9NZD8 CT55 Homo sapiens Q8WUE5 32296183
Intra
SPG21 Q9NZD8 CT55 Homo sapiens Q8WUE5 32296183
Intra
SPG21 Q9NZD8 CRYAA Homo sapiens P02489 32296183
Intra
SPG21 Q9NZD8 CRYAA Homo sapiens P02489 25416956
Intra
SPG21 Q9NZD8 CRYAA Homo sapiens P02489 25416956
Intra
SPG21 Q9NZD8 CRYAA Homo sapiens P02489 32296183
Intra
SPG21 Q9NZD8 SH3GL1 Homo sapiens Q99961 32296183
Intra
SPG21 Q9NZD8 SH3GL1 Homo sapiens Q99961 32296183
Intra
SPG21 Q9NZD8 CIDEB Homo sapiens Q9UHD4 32296183
Intra
SPG21 Q9NZD8 CIDEB Homo sapiens Q9UHD4 32296183
Intra
SPG21 Q9NZD8 CIDEB Homo sapiens Q9UHD4 32296183
Intra
SPG21 Q9NZD8 SPRED2 Homo sapiens Q7Z698 32296183
Intra
SPG21 Q9NZD8 SPRED2 Homo sapiens Q7Z698 32296183
Intra
SPG21 Q9NZD8 SPRED2 Homo sapiens Q7Z698 25416956
Intra
SPG21 Q9NZD8 MYG1 Homo sapiens Q9HB07 32296183
Intra
SPG21 Q9NZD8 MYG1 Homo sapiens Q9HB07 32296183
Intra
SPG21 Q9NZD8 CDKN2B Homo sapiens P42772 32296183
Intra
SPG21 Q9NZD8 CDKN2B Homo sapiens P42772 32296183
Intra
SPG21 Q9NZD8 RABAC1 Homo sapiens Q9UI14 32296183
Intra
SPG21 Q9NZD8 RABAC1 Homo sapiens Q9UI14 25416956
Intra
SPG21 Q9NZD8 RABAC1 Homo sapiens Q9UI14 32296183
Intra
SPG21 Q9NZD8 RABAC1 Homo sapiens Q9UI14 32296183
Intra
SPG21 Q9NZD8 RABAC1 Homo sapiens Q9UI14 25416956
Intra
SPG21 Q9NZD8 ARL6IP1 Homo sapiens Q15041 32296183
Intra
SPG21 Q9NZD8 ARL6IP1 Homo sapiens Q15041 25416956
Intra
SPG21 Q9NZD8 ARL6IP1 Homo sapiens Q15041 32296183
Intra
SPG21 Q9NZD8 CUTC Homo sapiens Q9NTM9 31515488
Intra
SPG21 Q9NZD8 CUTC Homo sapiens Q9NTM9 32296183
Intra
SPG21 Q9NZD8 CUTC Homo sapiens Q9NTM9 25416956
Intra
SPG21 Q9NZD8 CUTC Homo sapiens Q9NTM9 25416956
Intra
SPG21 Q9NZD8 CUTC Homo sapiens Q9NTM9 32296183
Intra
SPG21 Q9NZD8 MPC2 Homo sapiens O95563 32296183
Intra
SPG21 Q9NZD8 MPC2 Homo sapiens O95563 32296183
Intra
SPG21 Q9NZD8 TRIM9 Homo sapiens Q9C026 32296183
Intra
SPG21 Q9NZD8 TRIM9 Homo sapiens Q9C026 25416956
Intra
SPG21 Q9NZD8 TRIM9 Homo sapiens Q9C026 32296183
Intra
SPG21 Q9NZD8 TCF12 Homo sapiens Q99081 25416956
Intra
SPG21 Q9NZD8 DCTPP1 Homo sapiens Q9H773 32296183
Intra
SPG21 Q9NZD8 DCTPP1 Homo sapiens Q9H773 32296183
Intra
SPG21 Q9NZD8 PEF1 Homo sapiens Q9UBV8 32296183
Intra
SPG21 Q9NZD8 PEF1 Homo sapiens Q9UBV8 32296183
Intra
SPG21 Q9NZD8 PEF1 Homo sapiens Q9UBV8 32296183
Intra
SPG21 Q9NZD8 PRTFDC1 Homo sapiens Q9NRG1 32296183
Intra
SPG21 Q9NZD8 PRTFDC1 Homo sapiens Q9NRG1 32296183
Intra
SPG21 Q9NZD8 LNX1 Homo sapiens Q8TBB1 32296183
Intra
SPG21 Q9NZD8 LNX1 Homo sapiens Q8TBB1 32296183
Intra
SPG21 Q9NZD8 USHBP1 Homo sapiens Q8N6Y0 32296183
Intra
SPG21 Q9NZD8 USHBP1 Homo sapiens Q8N6Y0 32296183
Intra
SPG21 Q9NZD8 TRIM23 Homo sapiens P36406 25416956
Intra
SPG21 Q9NZD8 DTX2 Homo sapiens Q86UW9 32296183
Intra
SPG21 Q9NZD8 DTX2 Homo sapiens Q86UW9 32296183
Intra
SPG21 Q9NZD8 CTPS2 Homo sapiens Q9NRF8 25416956
Intra
SPG21 Q9NZD8 CTPS2 Homo sapiens Q9NRF8 16189514
Intra
SPG21 Q9NZD8 NIF3L1 Homo sapiens Q9GZT8 32296183
Intra
SPG21 Q9NZD8 NIF3L1 Homo sapiens Q9GZT8 32296183
Intra
SPG21 Q9NZD8 NUP54 Homo sapiens Q7Z3B4 32296183
Intra
SPG21 Q9NZD8 NUP54 Homo sapiens Q7Z3B4 32296183
Intra
SPG21 Q9NZD8 AGTRAP Homo sapiens Q6RW13 25416956
Intra
SPG21 Q9NZD8 AGTRAP Homo sapiens Q6RW13 25416956
Intra
SPG21 Q9NZD8 AGTRAP Homo sapiens Q6RW13
Y2H
21516116
Intra
SPG21 Q9NZD8 SORBS3 Homo sapiens O60504 32296183
Intra
SPG21 Q9NZD8 SORBS3 Homo sapiens O60504 32296183
Intra
SPG21 Q9NZD8 KRT19 Homo sapiens P08727 32296183
Intra
SPG21 Q9NZD8 KRT19 Homo sapiens P08727 32296183
Intra
SPG21 Q9NZD8 CEP76 Homo sapiens Q8TAP6 32296183
Intra
SPG21 Q9NZD8 CEP76 Homo sapiens Q8TAP6 32296183
Intra
SPG21 Q9NZD8 ARMC7 Homo sapiens Q9H6L4 32296183
Intra
SPG21 Q9NZD8 ARMC7 Homo sapiens Q9H6L4 32296183
Intra
SPG21 Q9NZD8 AKIRIN2 Homo sapiens Q53H80 32296183
Intra
SPG21 Q9NZD8 AKIRIN2 Homo sapiens Q53H80 32296183
Intra
SPG21 Q9NZD8 AKIRIN2 Homo sapiens Q53H80 16189514
Intra
SPG21 Q9NZD8 SSBP4 Homo sapiens Q9BWG4 32296183
Intra
SPG21 Q9NZD8 SSBP4 Homo sapiens Q9BWG4 32296183
Intra
SPG21 Q9NZD8 NME4 Homo sapiens O00746 32296183
Intra
SPG21 Q9NZD8 NME4 Homo sapiens O00746 32296183
Intra
SPG21 Q9NZD8 ZNF581 Homo sapiens Q9P0T4 32296183
Intra
SPG21 Q9NZD8 ZNF581 Homo sapiens Q9P0T4 32296183
Intra
SPG21 Q9NZD8 ZNF581 Homo sapiens Q9P0T4 32296183
Intra
SPG21 Q9NZD8 IKZF3 Homo sapiens Q9UKT9 25416956
Intra
SPG21 Q9NZD8 IKZF3 Homo sapiens Q9UKT9 32296183
Intra
SPG21 Q9NZD8 IKZF3 Homo sapiens Q9UKT9 32296183
Intra
SPG21 Q9NZD8 IKZF3 Homo sapiens Q9UKT9 25416956
Intra
SPG21 Q9NZD8 IKZF3 Homo sapiens Q9UKT9 32296183
Intra
SPG21 Q9NZD8 IKZF3 Homo sapiens Q9UKT9 25416956
Intra
SPG21 Q9NZD8 PAX6 Homo sapiens P26367 32296183
Intra
SPG21 Q9NZD8 PAX6 Homo sapiens P26367 32296183
Intra
SPG21 Q9NZD8 CRX Homo sapiens O43186 32296183
Intra
SPG21 Q9NZD8 CRX Homo sapiens O43186 32296183
Intra
SPG21 Q9NZD8 HPRT1 Homo sapiens P00492 32296183
Intra
SPG21 Q9NZD8 HPRT1 Homo sapiens P00492 32296183
Intra
SPG21 Q9NZD8 PRPS1 Homo sapiens P60891 31515488
Intra
SPG21 Q9NZD8 PRPS1 Homo sapiens P60891 25416956
Intra
SPG21 Q9NZD8 PRPS1 Homo sapiens P60891 25416956
Intra
SPG21 Q9NZD8 PRPS1 Homo sapiens P60891 32296183
Intra
SPG21 Q9NZD8 TEKT4 Homo sapiens Q8WW24 32296183
Intra
SPG21 Q9NZD8 TEKT4 Homo sapiens Q8WW24 32296183
Intra
SPG21 Q9NZD8 LEPROTL1 Homo sapiens O95214 32296183
Intra
SPG21 Q9NZD8 LEPROTL1 Homo sapiens O95214 32296183
Intra
SPG21 Q9NZD8 BSND Homo sapiens Q8WZ55 32296183
Intra
SPG21 Q9NZD8 BSND Homo sapiens Q8WZ55 32296183
Intra
SPG21 Q9NZD8 LMO1 Homo sapiens P25800 32296183
Intra
SPG21 Q9NZD8 LMO1 Homo sapiens P25800 32296183
Intra
SPG21 Q9NZD8 NAB2 Homo sapiens Q15742 32296183
Intra
SPG21 Q9NZD8 NAB2 Homo sapiens Q15742 32296183
Intra
SPG21 Q9NZD8 TTC23L Homo sapiens Q6PF05 32296183
Intra
SPG21 Q9NZD8 TTC23L Homo sapiens Q6PF05 32296183
Intra
SPG21 Q9NZD8 PDE5A Homo sapiens O76074 32296183
Intra
SPG21 Q9NZD8 PDE5A Homo sapiens O76074 32296183
Intra
SPG21 Q9NZD8 SYP Homo sapiens P08247 32296183
Intra
SPG21 Q9NZD8 SYP Homo sapiens P08247 32296183
Intra
SPG21 Q9NZD8 COG3 Homo sapiens Q96JB2-2 32296183
Intra
SPG21 Q9NZD8 COG3 Homo sapiens Q96JB2-2 32296183
Intra
SPG21 Q9NZD8 GAD2 Homo sapiens Q05329 32296183
Intra
SPG21 Q9NZD8 GAD2 Homo sapiens Q05329 32296183
Intra
SPG21 Q9NZD8 KRT31 Homo sapiens Q15323 32296183
Intra
SPG21 Q9NZD8 KRT31 Homo sapiens Q15323 32296183
Intra
SPG21 Q9NZD8 SCAMP1 Homo sapiens O15126 32296183
Intra
SPG21 Q9NZD8 SCAMP1 Homo sapiens O15126 32296183
Cross
SPG21 Q9NZD8 tax Human T-cell leukemia virus P03410 22458338
Cross
SPG21 Q9NZD8 tax Human T-cell leukemia virus P03410 22458338
Intra
SPG21 Q9NZD8 TRIM50 Homo sapiens Q86XT4 32296183
Intra
SPG21 Q9NZD8 TRIM50 Homo sapiens Q86XT4 32296183
Intra
SPG21 Q9NZD8 ZNF629 Homo sapiens Q9UEG4 32296183
Intra
SPG21 Q9NZD8 ZNF629 Homo sapiens Q9UEG4 32296183
Intra
SPG21 Q9NZD8 ZNF629 Homo sapiens Q9UEG4 32296183
Cross: Cross-species interaction Intra: Intraspecies interaction

Recombinant SPG21 Proteins

Cat. No. Product Name Accession Purity
HY-P77212 SPG21 Protein, Human (sf9, His) Q9NZD8-1 (M1-Q308) ≥ 95%, as determined by reducing SDS-PAGE.

Related Diseases

Diseases Alias
Mast Syndrome
  • SPG21

  • Spastic Paraplegia 21, Autosomal Recessive

  • Autosomal Recessive Spastic Paraplegia Type 21

  • Autosomal Recessive Spastic Paraplegia 21

  • Hereditary Spastic Paraplegia 21

Paraplegia
  • Paraplegia, Lower

  • Severe Or Complete Loss Of Motor Function In The Lower Extremities And Lower Portions Of The Trunk

Hereditary Spastic Paraplegia
  • Familial Spastic Paraplegia

  • Hereditary Spastic Paraparesis

  • Strumpell-Lorrain Disease

  • Familial Spastic Paraparesis

  • Hsp

  • Spg

  • Strümpell-Lorrain Disease

  • Spastic Paraplegia, Hereditary

  • French Settlement Disease

  • Strumpell-Lorrain Syndrome

  • Fsp

  • Spastic Paraplegia, Familial

  • Spastic Paraplegia Hereditary

  • Spastic Paraplegia 3, Autosomal Dominant

  • Spastic Paraparesis

  • Hereditary Spastic Paralysis

  • Familial Spastic Paralysis

  • Hereditary Spastic Ataxia

Spastic Paraplegia 11, Autosomal Recessive
  • SPG11

  • Hereditary Spastic Paraplegia 11

  • Hsp-Tcc

  • Autosomal Recessive Spastic Paraplegia Type 11

  • Nakamura-Osame Syndrome

  • Spastic Paraplegia-Intellectual Disability-Thin Corpus Callosum Syndrome

  • Spastic Paraplegia, Autosomal Recessive, With Mental Impairment And Thin Corpus Callosum

  • Spastic Paraplegia, Autosomal Recessive, Complicated, With Thin Corpus Callosum

  • Autosomal Recessive Spastic Paraplegia 11

  • Autosomal Recessive Spastic Paraplegia Complicated With Thin Corpus Callosum

  • Autosomal Recessive Spastic Paraplegia With Mental Impairment And Thin Corpus Callosum

  • Arhsp-Tcc

  • Autosomal Recessive Spastic Paraplegia With Thinning Of Corpus Callosum

  • Spastic Paraplegia Autosomal Recessive Complicated With Thin Corpus Callosum

  • Spastic Paraplegia Autosomal Recessive With Mental Impairment And Thin Corpus Callosum

  • Paraplegia, Spastic, Autosomal Recessive, Type 11

  • Nakamura Osame Syndrome

Hereditary Spastic Paraplegia 23
  • Lison Syndrome

  • Spastic Paraparesis-Vitiligo-Premature Graying-Characteristic Facies Syndrome

  • Spastic Paraplegia 23

  • Spastic Paraplegia With Pigmentary Abnormalities

  • Spg23

Spastic Paraplegia 27, Autosomal Recessive
  • SPG27

  • Hereditary Spastic Paraplegia 27

  • Autosomal Recessive Spastic Paraplegia Type 27

  • Autosomal Recessive Spastic Paraplegia 27

  • Spastic Paraplegia-27, Autosomal Recessive

Spastic Paraplegia 63, Autosomal Recessive
  • SPG63

  • Hereditary Spastic Paraplegia 63

  • Spastic Paraplegia 63

  • Autosomal Recessive Spastic Paraplegia 63

  • Autosomal Recessive Spastic Paraplegia Type 63

  • Paraplegia, Spastic, Type 63, Autosomal Recessive

Spastic Paraplegia 44, Autosomal Recessive
  • SPG44

  • Hereditary Spastic Paraplegia 44

  • Autosomal Recessive Spastic Paraplegia 44

  • Autosomal Recessive Spastic Paraplegia Type 44

  • Paraplegia, Spastic, Type 44, Autosomal Recessive

Spastic Paraplegia 55, Autosomal Recessive
  • SPG55

  • Hereditary Spastic Paraplegia 55

  • Autosomal Recessive Spastic Paraplegia Type 55

  • Autosomal Recessive Spastic Paraplegia 55

  • Paraplegia, Spastic, Autosomal Recessive, Type 55

Spastic Paraplegia 41, Autosomal Dominant
  • SPG41

  • Hereditary Spastic Paraplegia 41

  • Autosomal Dominant Spastic Paraplegia Type 41

  • Autosomal Dominant Spastic Paraplegia 41

Spastic Paraplegia 19, Autosomal Dominant
  • SPG19

  • Hereditary Spastic Paraplegia 19

  • Autosomal Dominant Spastic Paraplegia Type 19

  • Autosomal Dominant Spastic Paraplegia 19

  • Spastic Paraplegia 19

  • Spastic Paraplegia-19

Charcot-Marie-Tooth Disease Type 2a2a
  • Charcot-Marie-Tooth Disease, Type 2a2a

  • Autosomal Dominant Axonal Charcot-Marie-Tooth Disease Type 2a2

  • Charcot-Marie-Tooth Neuronal Type 2a2

  • Charcot-Marie-Tooth Neuropathy Type 2a2

  • Cmt2a2a

  • Hereditary Motor And Sensory Neuropathy Iia2

  • Hmsn Iia2

  • Hmsn2a2

Spastic Paraplegia 54, Autosomal Recessive
  • SPG54

  • Hereditary Spastic Paraplegia 54

  • Autosomal Recessive Spastic Paraplegia Type 54

  • Autosomal Recessive Spastic Paraplegia 54

  • Paraplegia, Spastic, Type 54, Autosomal Recessive

Spastic Paraplegia 36, Autosomal Dominant
  • SPG36

  • Hereditary Spastic Paraplegia 36

  • Autosomal Dominant Spastic Paraplegia Type 36

  • Autosomal Dominant Spastic Paraplegia 36

Spastic Paraplegia 15, Autosomal Recessive
  • SPG15

  • Kjellin Syndrome

  • Hereditary Spastic Paraplegia 15

  • Spastic Paraplegia And Retinal Degeneration

  • Autosomal Recessive Spastic Paraplegia Type 15

  • Hereditary Spastic Paraparesis Type 15

  • Spastic Paraplegia-Retinal Degeneration Syndrome

  • Autosomal Recessive Spastic Paraplegia 15

Charcot-Marie-Tooth Disease, Axonal, Type 2h
  • CMT2H

  • Charcot-Marie-Tooth Disease Axonal Type 2h

  • Ar-Cmt2c

  • Autosomal Recessive Axonal Cmt4c2

  • Axonal Charcot-Marie-Tooth Disease With Pyramidal Involvement

  • Charcot-Marie-Tooth Disease Type 2h

  • Charcot-Marie-Tooth Disease, Axonal, With Pyramidal Features, Autosomal Recessive

  • Charcot-Marie-Tooth Neuropathy, Axonal, With Pyramidal Features, Autosomal Recessive

  • Autosomal Recessive Axonal Charcot-Marie-Tooth Disease With Pyramidal Features

  • Autosomal Recessive Axonal Charcot-Marie-Tooth Neuropathy With Pyramidal Features

  • Charcot-Marie-Tooth Disease, Type 2h

Hereditary Spastic Paraplegia 49
  • Autosomal Recessive Spastic Paraplegia Type 49

  • Autosomal Recessive Spastic Paraplegia 49

  • Spg49

  • Paraplegia, Spastic, Type 49, Autosomal Recessive

Spastic Paraplegia 34, X-Linked
  • SPG34

  • Hereditary Spastic Paraplegia 34

  • X-Linked Spastic Paraplegia Type 34

  • X-Linked Spastic Paraplegia 34

Spastic Paraplegia 20, Autosomal Recessive
  • Troyer Syndrome

  • SPG20

  • Spastic Paraparesis, Childhood-Onset, With Distal Muscle Wasting

  • Spastic Paraplegia, Autosomal Recessive, Troyer Type

  • Autosomal Recessive Spastic Paraplegia Type 20

  • Autosomal Recessive Hereditary Spastic Paraplegia

  • Spastic Paraplegia 20

  • Cross-Mckusick Syndrome

  • Autosomal Recessive Spastic Paraplegia 20

  • Autosomal Recessive Spastic Paraplegia Troyer Type

  • Childhood-Onset Spastic Paraparesis With Distal Muscle Wasting

  • Hereditary Spastic Paraplegia 20

  • Spastic Paraplegia Type 20

  • Hereditary Spastic Paraplegia

  • Childhood-Onset Spastic Paraparesis-Distal Muscle Wasting Syndrome

  • Spastic Paraparesis Childhood-Onset With Distal Muscle Wasting

  • Spastic Paraplegia Autosomal Recessive Troyer Type

  • Trs

  • Spastic Paraplegia Hereditary Autosomal Recessive

  • Spastic Paraplegia, Hereditary

Spastic Paraplegia 18, Autosomal Recessive
  • SPG18

  • Idmdc

  • Hereditary Spastic Paraplegia 18

  • Intellectual Disability, Motor Dysfunction, And Joint Contractures

  • Autosomal Recessive Spastic Paraplegia Type 18

  • Autosomal Recessive Spastic Paraplegia 18

  • Intellectual Disability, Motor Dysfunction And Joint Contractures

  • Spastic Paraplegia 18

  • Intellectual Disability Motor Dysfunction And Joint Contractures

  • Paraplegia, Spastic, Type 18

Spastic Paraplegia 64, Autosomal Recessive
  • SPG64

  • Hereditary Spastic Paraplegia 64

  • Autosomal Recessive Spastic Paraplegia Type 64

  • Autosomal Recessive Spastic Paraplegia 64

  • Paraplegia, Spastic, Type 64, Autosomal Recessive

Masa Syndrome
  • L1 Syndrome

  • Crash Syndrome

  • X-Linked Hydrocephalus Syndrome

  • SPG1

  • Gareis-Mason Syndrome

  • Spastic Paraplegia 1, X-Linked

  • Corpus Callosum Hypoplasia-Retardation-Adducted Thumbs-Spasticity-Hydrocephalus Syndrome

  • L1cam Syndrome

  • Spastic Paraplegia 1

  • Mental Retardation, Aphasia, Shuffling Gait, And Adducted Thumbs

  • Clasped Thumb And Mental Retardation

  • Thumb, Congenital Clasped, With Mental Retardation

  • Adducted Thumb With Mental Retardation

  • Hereditary Spastic Paraplegia 1

  • X-Linked Complicated Hereditary Spastic Paraplegia Type 1

  • X-Linked Corpus Callosum Agenesis

  • X-Linked Spastic Paraplegia 1

  • L1 Disease

  • X-Linked Intellectual Disability - Corpus Callosum Agenesis - Spastic Quadriparesis

  • Adducted Thumb With Intellectual Disability

  • Clasped Thumb And Intellectual Disability

  • Intellectual Disability Aphasia Shuffling Gait Adducted Thumbs

  • Thumb Congenital Clasped With Intellectual Disability

  • X-Linked Intellectual Disability-Corpus Callosum Agenesis-Spastic Quadriparesis Syndrome

  • Adducted Thumbs-Mental Retardation Syndrome

  • Corpus Callosum Hypoplasia, Mental Retardation, Adducted Thumbs, Spastic Paraplegia, Hydrocephalus Syndrome

  • Mental Retardation-Clasped Thumb Syndrome

  • Intellectual Disability-Aphasia-Shuffling Gait-Adducted Thumbs Syndrome

  • Spastic Paraplegia Type 1, X-Linked

  • MASA

  • Corpus Callosum Hypoplasia-Psychomotor Retardation, Adducted Thumbs-Spastic Paraparesis-Hydrocephalus

  • Crash

  • Masa Syndrome

Spastic Paraplegia 26, Autosomal Recessive
  • SPG26

  • Hereditary Spastic Paraplegia 26

  • Autosomal Recessive Spastic Paraplegia Type 26

  • Gm2 Synthase Deficiency

  • Spastic Paraplegia 26

  • Autosomal Recessive Spastic Paraplegia 26

  • Paraplegia, Spastic, Autosomal Recessive, Type 26

Hereditary Spastic Paraplegia 35
  • Autosomal Recessive Spastic Paraplegia Type 35

  • Spg35

  • Autosomal Recessive Spastic Paraplegia 35

  • Fahn

  • Fatty Acid Hydroxylase-Associated Neurodegeneration

  • Leukodystrophy, Dysmyelinating And Spastic Paraparesis With Or Without Dystonia

Charcot-Marie-Tooth Disease, Recessive Intermediate D
  • Charcot-Marie-Tooth Disease Recessive Intermediate D

  • CMTRID

  • Autosomal Recessive Intermediate Charcot-Marie-Tooth Disease Type D

  • Ri-Cmt Type D

  • Charcot-Marie-Tooth Disease, Recessive, Intermediate Type, D

Spastic Paraplegia 47, Autosomal Recessive
  • Hereditary Spastic Paraplegia 47

  • SPG47

  • Cpsq5

  • Cerebral Palsy, Spastic Quadriplegic, 5, Formerly

  • Cpsq5, Formerly

  • Autosomal Recessive Spastic Paraplegia 47

  • Spastic Quadriplegic Cerebral Palsy 5

  • Cerebral Palsy, Spastic Quadriplegic 5

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

Hereditary Spastic Paraplegia 30
  • Autosomal Spastic Paraplegia Type 30

  • Spg30

  • Autosomal Recessive Spastic Paraplegia 30

Spastic Paraplegia 13, Autosomal Dominant
  • SPG13

  • Hereditary Spastic Paraplegia 13

  • Autosomal Dominant Spastic Paraplegia 13

  • Spastic Paraplegia 13

  • Autosomal Dominant Spastic Paraplegia Type 13

  • Spastic Paraplegia-13

  • Paraplegia, Spastic, Type 13

Spastic Paraplegia 61, Autosomal Recessive
  • SPG61

  • Hereditary Spastic Paraplegia 61

  • Autosomal Recessive Spastic Paraplegia Type 61

  • Autosomal Recessive Spastic Paraplegia 61

  • Paraplegia, Spastic, Type 61, Autosomal Recessive

Neuropathy, Hereditary Sensory, Type Iic
  • HSN2C

  • Hereditary Sensory Neuropathy Type 2c

  • Hereditary Sensory Neuropathy Type Iic

  • Neuropathy, Hereditary Sensory, Type 2c

  • Neuropathy, Hereditary Sensory, 2c

  • Hsn Iice

  • Neuropathy, Sensory, Hereditary, Type Iic

Spastic Paraplegia 45, Autosomal Recessive
  • SPG45

  • Hereditary Spastic Paraplegia 45

  • Autosomal Recessive Spastic Paraplegia Type 45

  • Autosomal Recessive Spastic Paraplegia Type 65

  • Spg65

  • Autosomal Recessive Spastic Paraplegia 45

  • Paraplegia, Spastic, Type 45, Autosomal Recessive

Hyperuricemia, Hprt-Related
  • Hprt-Related Gout

  • Kelley-Seegmiller Syndrome

  • Hprt Deficiency, Partial

  • HRH

  • Gout, Hprt-Related

  • Hprt1 Deficiency, Partial

  • Hrpt-Related Hyperuricemia

  • Hprt Deficiency, Grade I

  • Hprt Partial Deficiency

  • Hprt-Related Hyperuricemia

  • Hprt1 Partial Deficiency

  • Hypoxanthine Guanine Phosphoribosyltransferase 1 Partial Deficiency

  • Hypoxanthine Guanine Phosphoribosyltransferase Deficiency, Grade I

  • Hypoxanthine Guanine Phosphoribosyltransferase Partial Deficiency

  • Partial Hypoxanthine-Guanine Phosphoribosyltransferase Deficiency

  • Hypoxanthine Guanine Phosphoribosyltransferase 1 Deficiency, Partial

  • Hyperuricemia, Hrpt-Related

Spastic Paraplegia 2, X-Linked
  • SPG2

  • Hereditary Spastic Paraplegia 2

  • Sppx2

  • Spastic Paraplegia Type 2

  • Spastic Paraplegia 2

  • Hereditary X-Linked Recessive Spastic Paraplegia

  • X-Linked Spastic Paraplegia 2

  • X Linked Recessive Hereditary Spastic Paraplegia

  • Spastic Gait Type 2

  • Spastic Paraparesis Type 2

  • X-Linked Spastic Paraplegia Type 2

  • Spastic Paraplegia Type 2, X-Linked

  • Spastic Paraplegia-2

  • Paraplegia, Spastic, Type 2

Spastic Paraplegia 14, Autosomal Recessive
  • SPG14

  • Hereditary Spastic Paraplegia 14

  • Autosomal Recessive Spastic Paraplegia Type 14

  • Autosomal Recessive Spastic Paraplegia 14

  • Spastic Paraplegia 14

Spastic Paraplegia 73, Autosomal Dominant
  • SPG73

  • Hereditary Spastic Paraplegia 73

  • Autosomal Dominant Spastic Paraplegia Type 73

  • Autosomal Dominant Spastic Paraplegia 73

  • Paraplegia, Spastic, Autosomal Dominant, Type 73

Spastic Paraplegia 78, Autosomal Recessive
  • SPG78

  • Autosomal Recessive Spastic Paraplegia Type 78

  • Hereditary Spastic Paraplegia 78

  • Spastic Paraplegia 78 Autosomal Recessive

  • Doid:0112348

Charcot-Marie-Tooth Disease, Axonal, Type 2t
  • CMT2T

  • Charcot-Marie-Tooth Disease Axonal Type 2t

  • Charcot-Marie-Tooth Neuropathy, Type 2t

  • Charcot-Marie-Tooth Disease, Axonal, Autosomal Recessive, Type 2t

  • Ar-Cmt2t

  • Autosomal Recessive Axonal Charcot-Marie-Tooth Disease Type 2t

  • Mme-Related Autosomal Dominant Charcot Marie Tooth Disease Type 2

  • Charcot-Marie-Tooth Neuropathy Type 2t

  • Charcot-Marie-Tooth Disease Type 2t

  • Mme-Related Autosomal Dominant Cmt2

  • Mme-Related Autosomal Dominant Hereditary Motor And Sensory Neuropathy Type 2

  • Charcot-Marie-Tooth Disease 2t

  • Charcot-Marie-Tooth Neuropathy Axonal Type 2t

Agenesis Of The Corpus Callosum With Peripheral Neuropathy
  • Andermann Syndrome

  • Charlevoix Disease

  • ACCPN

  • Polyneuropathy, Sensorimotor, With Or Without Agenesis Of The Corpus Callosum

  • Corpus Callosum, Agenesis Of, With Neuronopathy

  • Corpus Callosum Agenesis-Neuronopathy Syndrome

  • Agenesis Of Corpus Callosum With Neuronopathy

  • Agenesis Of Corpus Callosum With Peripheral Neuropathy

  • Agenesis Of Corpus Callosum With Polyneuropathy

  • Corpus Callosum Agenesis Neuronopathy

  • Hmsn/Acc

  • Hereditary Motor And Sensory Neuropathy With Agenesis Of The Corpus Callosum

  • Agenesis Of The Corpus Callosum, With Peripheral Neuropathy

  • Andermann'S Syndrome

  • Agenesis, Corpus Callosum, With Peripheral Neuropathy

Spastic Paraplegia 10, Autosomal Dominant
  • SPG10

  • Hereditary Spastic Paraplegia 10

  • Autosomal Dominant Spastic Paraplegia Type 10

  • Spastic Paraplegia 10

  • Spastic Paraplegia 10 With Or Without Peripheral Neuropathy

  • Autosomal Dominant Spastic Paraplegia 10

  • Autosomal Dominant Spastic Paraplegia

  • Spastic Paraplegia, Autosomal Dominant

  • Paraplegia, Spastic, Autosomal Dominant, Type 10

Charcot-Marie-Tooth Disease, Axonal, Type 2b2
  • Charcot-Marie-Tooth Disease Type 2b2

  • CMT2B2

  • Arcmt2b

  • Charcot-Marie-Tooth Disease, Type 2b2

  • Ar-Cmt2b2

  • Autosomal Recessive Axonal Charcot-Marie-Tooth Disease Type 2b2

  • Autosomal Recessive Axonal Cmt4c3

  • Charcot-Marie-Tooth Disease Neuronal Type 2b2

  • Charcot-Marie-Tooth Neuropathy Type 2b2

  • Charcot-Marie-Tooth Disease, Axonal, Autosomal Recessive, Type 2b2

  • Charcot-Marie-Tooth Disease, Neuronal, Type 2b2

  • Charcot-Marie-Tooth Neuropathy, Type 2b2

  • Charcot-Marie-Tooth Disease 2b2

  • Charcot-Marie-Tooth Disease Axonal Autosomal Recessive B2

  • Charcot-Marie-Tooth Disease Axonal Type 2b2

Spastic Paraplegia 42, Autosomal Dominant
  • SPG42

  • Hereditary Spastic Paraplegia 42

  • Autosomal Dominant Spastic Paraplegia Type 42

  • Autosomal Dominant Spastic Paraplegia 42

  • Paraplegia, Spastic, Type 42, Autosomal Dominant

Charcot-Marie-Tooth Disease, Axonal, Type 2e
  • Charcot-Marie-Tooth Disease Type 2

  • CMT2E

  • CMT2S

  • CMT2Y

  • Charcot-Marie-Tooth Disease Type 2e

  • Charcot-Marie-Tooth Disease Type 2y

  • Charcot-Marie-Tooth Disease Axonal Type 2s

  • Charcot-Marie-Tooth Disease, Axonal, Type 2s

  • Charcot-Marie-Tooth Disease, Type 2e

  • Hereditary Motor And Sensory Neuropathy Type 2

  • Charcot-Marie-Tooth Neuropathy, Type 2s

  • Charcot-Marie-Tooth Disease, Axonal, Autosomal Recessive, Type 2s

  • Charcot-Marie-Tooth Disease, Axonal, Type 2y

  • Charcot-Marie-Tooth Disease, Axonal, Autosomal Dominant, Type 2y

  • Charcot-Marie-Tooth Neuropathy, Type 2y

  • Charcot-Marie-Tooth Disease, Type 2y

  • Autosomal Dominant Charcot-Marie-Tooth Disease Type 2e

  • Charcot-Marie-Tooth Neuropathy Type 2e

  • Autosomal Dominant Charcot-Marie-Tooth Disease Type 2 Due To Vcp Mutation

  • Cmt2 Due To Vcp Mutation

  • Charcot-Marie-Tooth Disease Type 2s

  • Autosomal Dominant Charcot-Marie-Tooth Disease Type 2

  • Autosomal Dominant Axonal Charcot-Marie-Tooth Disease

  • Cmt2

  • Charcot-Marie-Tooth Neuropathy, Type 2e

  • Hereditary Motor And Sensory Neuropathy Guadalajara Neuronal Type

  • Hereditary Motor And Sensory Neuropathy Okinawa Type

  • Autosomal Dominant Axonal Charcot-Marie-Tooth Type 2y

  • Charcot-Marie-Tooth Neuropathy Type 2y

  • Autosomal Recessive Axonal Charcot-Marie-Tooth Type 2s

  • Charcot-Marie-Tooth Neuropathy Type 2s

  • Charcot-Marie-Tooth Type 2

  • Autosomal Dominant Charcot-Marie-Tooth Disease Type 2y

  • Charcot-Marie-Tooth Disease 2e

  • Charcot-Marie-Tooth Disease Axonal Type 2e

  • Charcot-Marie-Tooth Disease Neuronal Type 2e

  • Charcot-Marie-Tooth Disease 2s

  • Charcot-Marie-Tooth Neuropathy Axonal Type 2s

  • Charcot-Marie-Tooth Disease 2y

  • Charcot-Marie-Tooth Disease, Type 2

  • Hereditary Motor And Sensory-Neuropathy Type Ii

Spastic Paraplegia 17, Autosomal Dominant
  • Silver Syndrome

  • SPG17

  • Silver Spastic Paraplegia Syndrome

  • Spastic Paraplegia With Amyotrophy Of Hands And Feet

  • Hereditary Spastic Paraplegia 17

  • Autosomal Dominant Spastic Paraplegia Type 17

  • Spastic Paraplegia 17

  • Spastic Paraplegia-Amyotrophy Of Hands And Feet

  • Autosomal Dominant Spastic Paraplegia 17

  • Dhmn5b

  • Distal Hereditary Motor Neuropathy Type 5b

  • Paraplegia, Spastic, Autosomal Dominant, Type 17

  • Russell-Silver Syndrome

  • Neuronopathy, Distal Hereditary Motor, Type Vb

Spastic Ataxia
  • Spax

  • Ataxia, Spastic

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
Canis familiaris SPG21 VGNC VGNC:46735
Rattus norvegicus SPG21 RGD RGD:1359141
Macaca mulatta SPG21 VGNC VGNC:77970
Mus musculus SPG21 MGD MGI:106403
Felis catus SPG21 VGNC VGNC:65634
Bos taurus SPG21 VGNC VGNC:35208
Others SPG21 NCBI