1. Gene
  2. ARL5B - ADP ribosylation factor like GTPase 5B Gene

ARL5B - ADP ribosylation factor like GTPase 5B Gene

Homo sapiens

Also known as ARL8

Gene ID: 221079 | Gene type: protein coding

About ARL5B

Cytogenetic location: 10p12.31 Genomic coordinates (GRCh38): 10:18,659,431-18,681,639 (from NCBI)

This gene has 1 transcript (splice variant), 200 orthologues and 30 paralogues. Ubiquitous expression in adrenal (RPKM 13.8), gall bladder (RPKM 10.5) and 25 other tissues.

Summary

ARL5B (ARL8) belongs to a family of proteins that are structurally similar to ADP-ribosylation factors (ARFs; see MIM 103180). ARLs and ARFs are part of the Ras superfamily of regulatory GTPases.[supplied by OMIM, Nov 2010]

ARL5B Products(1)

mRNA Protein Name
NM_178815.5 NP_848930.1 ADP-ribosylation factor-like protein 5B
Gene Ontology
  • Molecular Function
  • Biological Process
Molecular Function GO Annotation Evidence Reference Source
enables protein binding IPI
IPI: Inferred from physical interaction
32296183 GOA
Biological Process GO Annotation Evidence Reference Source
involved in protein localization to Golgi membrane IMP
IMP: Inferred from mutant phenotype
25795912 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

ARL5B Protein Structure

Arf

Arf: ADP-ribosylation factor family (5 - 175)

  • 0
  • 100
  • 179 a.a.
Protein Preferred Names Protein Names

ADP-ribosylation factor-like protein 5B

ADP-ribosylation factor-like 5B

Related Diseases

Diseases Alias
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

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 ARL5B VGNC VGNC:38116
Felis catus ARL5B VGNC VGNC:59925
Bos taurus ARL5B VGNC VGNC:26148
Macaca mulatta ARL5B VGNC VGNC:69886
Mus musculus ARL5B MGD MGI:1923119
Rattus norvegicus ARL5B RGD RGD:1305569