RAB23 - RAB23, member RAS oncogene family Gene

Homo sapiens

Also known as HSPC137

Gene ID: 51715 | Gene type: protein coding

About RAB23

Cytogenetic location: 6p12.1-p11.2 Genomic coordinates (GRCh38): 6:57,186,992-57,222,307 (from NCBI)

This gene has 2 transcripts (splice variants), 218 orthologues, 68 paralogues and is associated with 3 phenotypes. Broad expression in endometrium (RPKM 23.9), urinary bladder (RPKM 18.7) and 20 other tissues.

Summary

This gene encodes a small GTPase of the Ras superfamily. Rab proteins are involved in the regulation of diverse cellular functions associated with intracellular membrane trafficking, including Autophagy and immune response to Bacterial infection. The encoded protein may play a role in central nervous system development by antagonizing sonic Hedgehog signaling. Disruption of this gene has been implicated in Carpenter syndrome as well as Cancer. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]

RAB23 Products(5)

mRNA	Protein	Name
NM_001278666.2	NP_001265595.1	ras-related protein Rab-23
NM_001278667.2	NP_001265596.1	ras-related protein Rab-23
NM_001278668.2	NP_001265597.1	ras-related protein Rab-23
NM_016277.5	NP_057361.3	ras-related protein Rab-23
NM_183227.3	NP_899050.1	ras-related protein Rab-23

RAB23 Protein Structure

Ras

0
100
200
237 a.a.

Protein Preferred Names

Protein Names

ras-related protein Rab-23

RAB family small GTP binding protein RAB 23

Related Diseases

Diseases

Alias

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

Synostosis

Uveoparotid Fever

Heerfordt'S Syndrome

Chromosome 2q35 Duplication Syndrome

Syndactyly	Syndactyly Type 1
Sdty1	Zygodactyly
Syndactyly, Type I	Sd1
Syndactyly, Type 1, With Or Without Craniosynostosis	Symphalangism
Non-Syndromic Syndactyly	Symphalangy
Webbing Of Digits	Syndactyly, Type 1

Syndactyly, Type Iii

Syndactyly Type 3	SDTY3
Ring And Little Finger Syndactyly	Syndactyly Of Fingers Iv And V
Syndactyly Of Fingers 4 And 5	Ringand Little Finger Syndactyly
Syndactyly Of Fingers Four And Five	Syndactyly Of The Ring And Little Finger
Sd3	Syndactyly 3
Syndactyly Type Iii	4-5 Finger Syndactyly
Syndactyly, Type 3

Apert Syndrome

Acrocephalosyndactyly Type I	Acs1
Acrocephalosyndactylia	Acrocephalosyndactyly
Acs I	Apert-Crouzon Disease
Acrocephalosyndactyly Type 1	Acrocephalosyndactyly, Type I
Acs 1	Acrocephalo-Syndactyly Type 1
Syndactylic Oxycephaly	Apert'S Syndrome
Type I Acrocephalosyndactyly	APRS

Brachydactyly

Muenke Syndrome

Muenke Nonsyndromic Coronal Craniosynostosis	Fgfr3-Related Craniosynostosis
Fgfr3-Associated Coronal Synostosis	Coronal Craniosynostosis
MNKES	Syndrome Of Coronal Craniosynostosis
MNKS	Fgfr3-Related Isolated Coronal Synostosis
Muenke Non-Syndromic Coronal Craniosynostosis

Bardet-Biedl Syndrome

Bbs	Biedl-Bardet Syndrome

Polydactyly

Non-Syndromic Polydactyly	Polydactyly, Postaxial
Postaxial Polydactyly	Supernumerary Digit
Extra Digits	Hyperdactyly
Polydactylia	Polydactylism
Supernumerary Digits

Holoprosencephaly 5

HPE5	Holoprosencephaly-5
Holoprosencephaly, Type 5

Hydronephrosis

Stricture Of Ureteropelvic Junction With Hydronephrosis

Hydronephrosis With Ureteral Stricture, Not Elsewhere Classified

Saethre-Chotzen Syndrome

SCS	Acs3
Acs Iii	Chotzen Syndrome
Acrocephaly, Skull Asymmetry, And Mild Syndactyly	Acrocephalosyndactyly Type 3
Acrocephalosyndactyly, Type Iii	Acrocephalosyndactyly Type Iii
Saethre-Chotzen Syndrome With Or Without Eyelid Anomalies	Auralcephalosyndactyly
Acs 3	Acrocephalo-Syndactyly, Type 3
Blepharophimosis,Epicanthus Inversus, And Ptosis 3	Aural Cephalosyndactyly
Kurczynski-Casperson Syndrome	Acrocephalosyndactyly Iii
Dysostosis Craniofacialis With Hypertelorism	Saethre-Chotzen Syndrome, With/Without Eyelid Anomalies
Sakati Syndrome

Basal Cell Nevus Syndrome

Nevoid Basal Cell Carcinoma Syndrome	Gorlin Syndrome
Nbccs	BCNS
Gorlin-Goltz Syndrome	Multiple Basal Cell Nevi, Odontogenic Keratocysts, And Skeletal Anomalies
Cerebral Gigantism Jaw Cysts	Cramer Niederdellmann Syndrome
Gorlin Syndrome Or Gorlin-Goltz Syndrome	Naevoid Basal Cell Carcinoma Syndrome

Craniosynostosis

Premature Closure Of Cranial Sutures	Craniostenosis
Craniosynostosis Syndrome	Cso
Craniosynostoses	Congenital Ossification Of Cranial Sutures
Congenital Ossification Of Sutures Of Skull	Craniostosis
Imperfect Fusion Of Skull	Congenital Imperfect Closure Skull
Imperfect Closure Skull	Premature Closure Cranium Sutures
Deficiency Of Craniofacial Axis

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

Bioactive Molecules (1)

Cat. No.	Product Name	Effect	Purity	Rare Diseases
HY-RS11533	RAB23 Human Pre-designed siRNA Set A	Pre-designed Sets	/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Canis familiaris	RAB23	VGNC	VGNC:45263
Bos taurus	RAB23	VGNC	VGNC:33630
Macaca mulatta	RAB23	VGNC	VGNC:81523
Mus musculus	RAB23	MGD	MGI:99833
Rattus norvegicus	RAB23	RGD	RGD:1306867

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