RAB11A - RAB11A, member RAS oncogene family Gene

Also Known as YL8

Species: Homo sapiens

Gene Type: protein coding

Gene ID: 8766

About RAB11A

Cytogenetic location: 15q22.31 Genomic coordinates (GRCh38): 15:65,869,491-65,891,989 (from NCBI)

This gene has 9 transcripts (splice variants), 209 orthologues, 68 paralogues and is associated with 2 phenotypes. Ubiquitous expression in esophagus (RPKM 50.5), adrenal (RPKM 37.5) and 25 other tissues.

Summary

The protein encoded by this gene belongs to the Rab family of the small GTPase superfamily. It is associated with both constitutive and regulated secretory pathways, and may be involved in protein transport. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2011]

RAB11A Products (2)

mRNA	Protein	Name
NM_001206836.2	NP_001193765.1	ras-related protein Rab-11A isoform 2
NM_004663.5	NP_004654.1	ras-related protein Rab-11A isoform 1

Gene Ontology

Molecular Function
Biological Process
Cellular Component

Molecular Function GO Annotation	Evidence	References	Source
enables G protein activity	IDA IDA: Inferred from direct assay	15837192	GOA
enables GTPase activity	IDA IDA: Inferred from direct assay	15837192	GOA
enables dynein light intermediate chain binding	IDA IDA: Inferred from direct assay	20026645	GOA
enables microtubule binding	IDA IDA: Inferred from direct assay	24561039	GOA
enables myosin V binding	IPI IPI: Inferred from physical interaction	24006491	GOA
enables protein binding	IPI IPI: Inferred from physical interaction	12470645	GOA

Biological Process GO Annotation	Evidence	References	Source
involved in amyloid-beta clearance by transcytosis	IGI IGI: Inferred from genetic interaction	26005850	GOA
involved in astral microtubule organization	IMP IMP: Inferred from mutant phenotype	24561039	GOA
involved in early endosome to recycling endosome transport	IMP IMP: Inferred from mutant phenotype	20026645	GOA
involved in establishment of protein localization to membrane	IMP IMP: Inferred from mutant phenotype	24006491	GOA
involved in establishment of protein localization to organelle	IMP IMP: Inferred from mutant phenotype	24561039	GOA
involved in establishment of vesicle localization	IMP IMP: Inferred from mutant phenotype	24561039	GOA
involved in exosomal secretion	IMP IMP: Inferred from mutant phenotype	15634213	GOA
involved in mitotic metaphase chromosome alignment	IMP IMP: Inferred from mutant phenotype	24561039	GOA
involved in mitotic spindle assembly	IMP IMP: Inferred from mutant phenotype	24561039	GOA
involved in multivesicular body assembly	IMP IMP: Inferred from mutant phenotype	15634213	GOA
involved in neuron projection development	IMP IMP: Inferred from mutant phenotype	17082457	GOA
involved in positive regulation of G2/M transition of mitotic cell cycle	IMP IMP: Inferred from mutant phenotype	24561039	GOA
involved in positive regulation of epithelial cell migration	IMP IMP: Inferred from mutant phenotype	22613965	GOA
involved in positive regulation of mitotic cytokinetic process	IDA IDA: Inferred from direct assay	15601896	GOA
involved in protein localization to cilium	IDA IDA: Inferred from direct assay	25673879	GOA
involved in protein localization to plasma membrane	IDA IDA: Inferred from direct assay	17082457	GOA
involved in regulation of cilium assembly	IDA IDA: Inferred from direct assay	31204173	GOA
involved in regulation of cytokinesis	IMP IMP: Inferred from mutant phenotype	15601896	GOA
involved in regulation of early endosome to recycling endosome transport	IDA IDA: Inferred from direct assay	20026645	GOA
involved in regulation of endocytic recycling	IDA IDA: Inferred from direct assay	20026645	GOA
involved in regulation of multivesicular body size	IMP IMP: Inferred from mutant phenotype	15634213	GOA
involved in regulation of protein localization to centrosome	IDA IDA: Inferred from direct assay	20026645	GOA
involved in regulation of vesicle-mediated transport	IDA IDA: Inferred from direct assay	20026645	GOA
involved in regulation of vesicle-mediated transport	IMP IMP: Inferred from mutant phenotype	22613965	GOA
involved in vesicle-mediated transport	IDA IDA: Inferred from direct assay	17462998	GOA
involved in vesicle-mediated transport	IMP IMP: Inferred from mutant phenotype	20026645	GOA

Cellular Component GO Annotation	Evidence	References	Source
located in Golgi membrane	IDA IDA: Inferred from direct assay	25673879	GOA
colocalizes with centrosome	IDA IDA: Inferred from direct assay	24648492	GOA
located in centrosome	IDA IDA: Inferred from direct assay	25849865	GOA
located in cleavage furrow	IDA IDA: Inferred from direct assay	15601896	GOA
located in cytoplasmic vesicle	IDA IDA: Inferred from direct assay	22613965	GOA
located in endocytic vesicle membrane	IDA IDA: Inferred from direct assay	20026645	GOA
located in extracellular exosome	IDA IDA: Inferred from direct assay	15326289	GOA
is active in glutamatergic synapse	IDA IDA: Inferred from direct assay	26565907	GOA
is active in glutamatergic synapse	IMP IMP: Inferred from mutant phenotype	26565907	GOA
colocalizes with kinetochore microtubule	IDA IDA: Inferred from direct assay	24561039	GOA
located in multivesicular body	IDA IDA: Inferred from direct assay	15634213	GOA
located in phagocytic vesicle	IDA IDA: Inferred from direct assay	21255211	GOA
is active in postsynaptic recycling endosome	IDA IDA: Inferred from direct assay	26565907	GOA
is active in postsynaptic recycling endosome	IMP IMP: Inferred from mutant phenotype	26565907	GOA
part of protein-containing complex	IDA IDA: Inferred from direct assay	17462998	GOA
located in recycling endosome	IDA IDA: Inferred from direct assay	24561039	GOA
located in spindle pole	IDA IDA: Inferred from direct assay	24561039	GOA
located in trans-Golgi network	IDA IDA: Inferred from direct assay	15229288	GOA
located in trans-Golgi network membrane	IDA IDA: Inferred from direct assay	25673879	GOA
located in vesicle	IDA IDA: Inferred from direct assay	18570918	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

RAB11A Protein Structure

Ras

0
100
200
216 a.a.

Protein Preferred Names	Protein Names
ras-related protein Rab-11A	RAB 11A, member oncogene family

RAB11A Protein-protein interaction Information

Type	Protein Name	Protein ID	Interactor	Interactor Species	Interactor ID	Detection Method	References
Intra	RAB11A	P62491	RAB11FIP2	Homo sapiens	Q7L804	Anti Tag CoIP	33961781
Intra	RAB11A	P62491	RAB11FIP2	Homo sapiens	Q7L804	Pull Down	17082457
Intra	RAB11A	P62491	RAB11FIP2	Homo sapiens	Q7L804	Anti Tag CoIP	28514442
Intra	RAB11A	P62491	RAB11FIP2	Homo sapiens	Q7L804	BRET	29997244
Intra	RAB11A	P62491	RAB11FIP2	Homo sapiens	Q7L804	Lumier	32814053
Intra	RAB11A	P62491	RAB11FIP2	Homo sapiens	Q7L804	Validated Y2H	32296183
Intra	RAB11A	P62491	RAB11FIP2	Homo sapiens	Q7L804	Anti Tag CoIP	26496610
Intra	RAB11A	P62491	RAB11FIP2	Homo sapiens	Q7L804	Anti Tag CoIP	35271311
Intra	RAB11A	P62491	RAB11FIP2	Homo sapiens	Q7L804	Lumier	29997244
Intra	RAB11A	P62491	RAB11FIP5	Homo sapiens	Q9BXF6	Anti Tag CoIP	26496610
Intra	RAB11A	P62491	RAB11FIP5	Homo sapiens	Q9BXF6	Anti Tag CoIP	33961781
Intra	RAB11A	P62491	RAB11FIP5	Homo sapiens	Q9BXF6	BioID	29568061
Intra	RAB11A	P62491	RAB11FIP5	Homo sapiens	Q9BXF6	Anti Tag CoIP	28514442
Intra	RAB11A	P62491	RAB11FIP5	Homo sapiens	Q9BXF6	Anti Tag CoIP	35271311
Intra	RAB11A	P62491	RAB11FIP5	Homo sapiens	Q9BXF6	Pull Down	24591568
Intra	RAB11A	P62491	MYO5B	Homo sapiens	Q9ULV0-2	Validated Y2H	32296183
Intra	RAB11A	P62491	RAB11FIP3	Homo sapiens	O75154-1	Pull Down	17030804
Intra	RAB11A	P62491	RAB11FIP3	Homo sapiens	O75154-1	Solution Sedimentation	26258637
Intra	RAB11A	P62491	RAB11FIP3	Homo sapiens	O75154-1	Pull Down	24876499
Intra	RAB11A	P62491	RAB11FIP3	Homo sapiens	O75154-1	GMS	17030804
Intra	RAB11A	P62491	RAB11FIP3	Homo sapiens	O75154-1	Pull Down	26258637
Intra	RAB11A	P62491	RAB11FIP3	Homo sapiens	O75154-1	Y2H	17030804
Intra	RAB11A	P62491	RAB11FIP3	Homo sapiens	O75154-1	X-Ray Diffraction	17030804
Intra	RAB11A	P62491	RAB11FIP4	Homo sapiens	Q86YS3-1	Y2H	17030804
Intra	RAB11A	P62491	CHMP1B	Homo sapiens	Q7LBR1	Y2H	16730941
Intra	RAB11A	P62491	KLF15	Homo sapiens	Q9UIH9	Y2H Array	32814053
Intra	RAB11A	P62491	KLF15	Homo sapiens	Q9UIH9	Validated Y2H	32814053
Intra	RAB11A	P62491	KLF15	Homo sapiens	Q9UIH9	Y2H Pooling	32814053
Intra	RAB11A	P62491	ZFYVE27	Homo sapiens	Q5T4F4	Anti Tag CoIP	17082457
Intra	RAB11A	P62491	ZFYVE27	Homo sapiens	Q5T4F4	Pull Down	17082457
Intra	RAB11A	P62491	ITGB3BP	Homo sapiens	Q13352	Validated Y2H	32814053
Intra	RAB11A	P62491	ITGB3BP	Homo sapiens	Q13352	Y2H Pooling	32814053
Intra	RAB11A	P62491	ITGB3BP	Homo sapiens	Q13352	Y2H Array	32814053
Intra	RAB11A	P62491	RAB3IP	Homo sapiens	Q96QF0-2	Pull Down	26258637
Intra	RAB11A	P62491	RAB3IP	Homo sapiens	Q96QF0-2	Pull Down	20308558
Intra	RAB11A	P62491	RAB3IP	Homo sapiens	Q96QF0-2	ITC	26258637
Intra	RAB11A	P62491	RAB3IP	Homo sapiens	Q96QF0-2	X-Ray Diffraction	26258637
Intra	RAB11A	P62491	ZNF232	Homo sapiens	Q9UNY5	Validated Y2H	32814053
Intra	RAB11A	P62491	ZNF232	Homo sapiens	Q9UNY5	Y2H Array	32814053
Intra	RAB11A	P62491	ZNF232	Homo sapiens	Q9UNY5	Y2H Pooling	32814053
Intra	RAB11A	P62491	EVI5	Homo sapiens	O60447	Anti Tag CoIP	26496610
Intra	RAB11A	P62491	EVI5	Homo sapiens	O60447	Anti Tag CoIP	35271311

Cross: Cross-species interaction Intra: Intraspecies interaction

RAB11A Antibodies

Cat. No.	Product Name	Application	Reactivity
HY-P810819	RAB11A Antibody (YA10062)	WB, IHC-P	Human, Mouse, Rat
HY-P83231	Rab11A Antibody (YA2976)	WB, IP	Human, Mouse, Rat
HY-P86102	RB11 Antibody (YA5794)	WB, IHC-P, ICC/IF, IP, ELISA	Human, Mouse, Rat

Related Diseases

Diseases	Alias
Autosomal Dominant Non-Syndromic Intellectual Disability
Arthrogryposis, Renal Dysfunction, And Cholestasis 1	Arc Syndrome ARCS1 Arthrogryposis Renal Dysfunction Cholestasis Syndrome Arthrogryposis-Renal Dysfunction-Cholestasis Syndrome Arcs Arthrogryposis, Renal Dysfunction And Cholestasis Syndrome Arthrogryposis, Renal Dysfunction, And Cholestasis Arthrogryposis-Renal Dysfunction-Cholestasis Arthrogryposis - Renal Dysfunction - Cholestasis Arthrogryposis Multiplex Congenita, Renal Dysfunction, And Cholestasis Arthrogryposis, Renal Dysfunction And Cholestasis Syndrome 1 Arthrogryposis Renal Dysfunction And Cholestasis 1 Arthrogryposis With Renal Dysfunction And Cholestasis Syndrome Arthrogryposis, Renal Dysfunction, Cholestasis, Type 1 Kidney Failure Renal Insufficiency
Microvillus Inclusion Disease	Congenital Microvillous Atrophy Intractable Diarrhea Of Infancy Congenital Familial Protracted Diarrhea With Enterocyte Brush-Border Abnormalities Davidson Disease Microvillous Inclusion Disease Congenital Microvillus Atrophy Mvid Diarrhea 2 With Microvillus Atrophy Mvd Congenital Familial Protracted Diarrhea Davidson'S Disease Familial Enteropathy, Microvillus Microvillus Atrophy, Congenital Congenital Enteropathy Familial Protracted Enteropathy Microvillous Atrophy Microvillus Atrophy With Diarrhea 2 Idi
Charcot-Marie-Tooth Disease, Type 4c	Charcot-Marie-Tooth Disease Type 4c CMT4C Charcot-Marie-Tooth Neuropathy Type 4c Charcot-Marie-Tooth Disease, Demyelinating, Autosomal Recessive, Type 4c Charcot-Marie-Tooth Neuropathy, Type 4c Autosomal Recessive Demyelinating Charcot-Marie-Tooth Disease Type 4c Charcot-Marie-Tooth Disease 4c Charcot-Marie-Tooth Disease Demyelinating Autosomal Recessive 4c
Congenital Diarrhea
Carpenter Syndrome 1	Carpenter Syndrome Acrocephalopolysyndactyly Type Ii Acps Ii CRPT1 Acrocephalopolysyndactyly Type 2 Acrocephalosyndactyly, Type Ii Acrocephalopolysyndactyly 2 Acps2 Acps 2 Type Ii Acrocephalosyndactyly Carpenter Syndrome, Type 1 Apert-Crouzon Disease
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
Charcot-Marie-Tooth Disease, Axonal, Type 2b	Charcot-Marie-Tooth Disease Type 2b CMT2B Hmsn Iib Hmsn2b Charcot-Marie-Tooth Disease, Type 2b Hereditary Motor And Sensory Neuropathy Iib Autosomal Dominant Charcot-Marie-Tooth Disease Type 2b Charcot-Marie-Tooth Neuropathy Type 2b Charcot-Marie-Tooth Disease, Autosomal Dominant, Type 2b Charcot-Marie-Tooth Neuropathy, Type 2b Hereditary Motor And Sensory Nueropathy Iib Cmt 2b Charcot Marie Tooth Disease Type 2b Charcot-Marie-Tooth Disease, Neuronal, Type 2b Hereditary Motor And Sensory Neuropathy 2 B Peripheral Sensory Neuropathy, Autosomal Dominant Charcot-Marie-Tooth Disease 2b Charcot-Marie-Tooth Disease Axonal Type 2b Charcot-Marie-Tooth Disease Neuronal Type 2b Peripheral Sensory Neuropathy Autosomal Dominant Psn
Pontocerebellar Hypoplasia, Type 2e	Pontocerebellar Hypoplasia Type 2 Pontocerebellar Hypoplasia Type 2e Pch2 PCH2E Progressive Microcephaly From Birth Extrapyramidal Dyskinesia Chorea Epilepsy Pontocerebellar Hypoplasia 2e Pcca2 Progressive Cerebello-Cerebral Atrophy Type 2 Doid:0112328 Hypoplasia, Pontocerebellar, Type 2e Pontocerebellar Hypoplasia, Type 2d Pontocerebellar Hypoplasia Type 2a
Griscelli Syndrome	Chediak-Higashi-Like Syndrome Griscelli-Prunieras Syndrome Partial Albinism-Immunodeficiency Syndrome Griscelli Disease Gs Hypopigmentation Immunodeficiency Disease Partial Albinism With Immunodeficiency Immunodeficiency Syndrome With Hypopigmentation Hypopigmentation-Immunodeficiency Disease
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
Warburg Micro Syndrome 1	Warburg Micro Syndrome Micro Syndrome Warbm WARBM1 Warburg Sjo Fledelius Syndrome Warburg-Sjo-Fledelius Syndrome Micro Syndrome 1 Microcephaly, Microcornea, Congenital Cataract, Intellectual Disability, Optic Atrophy And Hypogenitalism
Cystic Fibrosis	Mucoviscidosis CF Pseudomonas Aeruginosa, Susceptibility To Chronic Infection By, In Cystic Fibrosis Pseudomonas Aeruginosa Chronic Infection By, In Cystic Fibrosis Cystic Fibrosis Lung Disease, Modifier Of Cystic Fibrosis Of Pancreas Fibrocystic Disease Of Pancreas Cf - [Cystic Fibrosis] Cystic Fibrosis Nos Fibrocystic Disease Fibrocystic Disease Of The Pancreas Mucoviscidosis Of Pancreas Nonproliferative Fibrocystic Disease Pancreatic Cystic Fibrosis
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
Hermansky-Pudlak Syndrome	Hps Albinism With Hemorrhagic Diathesis And Pigmented Reticuloendothelial Cells Hermanski-Pudlak Syndrome Hermansky Pudlak Syndrome Platelet Storage Pool Deficiency
Joubert Syndrome 1	Joubert Syndrome Jbts Cerebellooculorenal Syndrome 1 JBTS1 Joubert-Boltshauser Syndrome Cerebelloparenchymal Disorder Iv Cpd4 Cors1 Joubert Syndrome And Related Disorders Jsrd Familial Aplasia Of The Vermis Joubert Syndrome Related Disorders Js Cerebellar Vermis Agenesis Cerebelloparenchymal Disorder 4 Agenesis Of Cerebellar Vermis Cerebello-Oculo-Renal Syndrome Cors Joubert-Bolthauser Syndrome Cpd Iv Classic Joubert Syndrome Joubert Syndrome Type A Pure Joubert Syndrome Cerebello-Oculo-Renal Syndrome 1 Joubert Syndrome-1 Joubert Syndrome, Type 1 Joubert'S Syndrome
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
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
Cone-Rod Dystrophy 2	Cone-Rod Dystrophy CORD2 Cone-Rod Retinal Dystrophy Rcrd2 Cone-Rod Retinal Dystrophy 2 Crd2 Cord Crd Retinal Cone-Rod Dystrophy Cone-Rod Retinal Dystrophy-2 Retinal Cone-Rod Dystrophy 2 Tapetoretinal Degeneration Cone-Rod Degeneration Cone Rod Dystrophy Dystrophy, Cone-Rod Dystrophy, Cone-Rod, Type 2 Retinitis Pigmentosa Retinitis Pigmentosa 2 Progressive Cone-Rod Dystrophy
Retinitis Pigmentosa	RP Rod-Cone Dystrophy Autosomal Recessive Retinitis Pigmentosa Non-Syndromic Retinitis Pigmentosa Pericentral Pigmentary Retinopathy Pigmentary Retinopathy Tapetoretinal Degeneration Rcd Retinitis Pigmentosa Autosomal Recessive ARRP Retinitis Pigmentosa, Autosomal Recessive Retinitis Pigmentosa 1
Congenital Nervous System Abnormality	Congenital Neurologic Anomaly Congenital Nervous System Disorder
Fundus Dystrophy	Retinal Dystrophy Retinal Dystrophies Dystrophy, Retinal

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

Related Agents

Pre-clinical Phase

Pre-clinical Phase

Bioactive Molecules (1)

Cat. No.	Product Name	Effect	Purity	Rare Diseases
HY-RS11515	RAB11A Human Pre-designed siRNA Set A	Pre-designed Set	/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Mus musculus	RAB11A	MGD	MGI:1858202
Canis familiaris	RAB11A	VGNC	VGNC:45248
Rattus norvegicus	RAB11A	RGD	RGD:619762
Macaca mulatta	RAB11A	VGNC	VGNC:81517
Felis catus	RAB11A	VGNC	VGNC:97579
Bos taurus	RAB11A	VGNC	VGNC:33614
Others	RAB11A	NCBI