1. Gene
  2. ARF6 - ADP ribosylation factor 6 Gene

ARF6 - ADP ribosylation factor 6 Gene

Homo sapiens
Gene ID: 382 | Gene type: protein coding

About ARF6

Cytogenetic location: 14q21.3 Genomic coordinates (GRCh38): 14:49,893,082-49,897,054 (from NCBI)

This gene has 3 transcripts (splice variants), 197 orthologues and 30 paralogues. Ubiquitous expression in esophagus (RPKM 54.5), colon (RPKM 38.8) and 25 other tissues.

Summary

This gene encodes a member of the human ARF gene family, which is part of the Ras superfamily. The ARF genes encode small guanine nucleotide-binding proteins that stimulate the ADP-ribosyltransferase activity of cholera toxin and play a role in vesicular trafficking and as activators of Phospholipase D. The product of this gene is localized to the plasma membrane, and regulates vesicular trafficking, remodelling of membrane lipids, and signaling pathways that lead to actin remodeling. A pseudogene of this gene is located on chromosome 7. [provided by RefSeq, Jul 2008]

ARF6 Products(1)

mRNA Protein Name
NM_001663.4 NP_001654.1 ADP-ribosylation factor 6
Gene Ontology
  • Molecular Function
  • Biological Process
  • Cellular Component
Molecular Function GO Annotation Evidence Reference Source
enables G protein activity IDA
IDA: Inferred from direct assay
32103017 GOA
enables GDP binding IDA
IDA: Inferred from direct assay
15126638 GOA
enables GTP binding IDA
IDA: Inferred from direct assay
10391955 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
9312003 GOA
enables signaling adaptor activity IDA
IDA: Inferred from direct assay
37461827 GOA
enables thioesterase binding IPI
IPI: Inferred from physical interaction
15509780 GOA
Biological Process GO Annotation Evidence Reference Source
involved in cortical actin cytoskeleton organization IDA
IDA: Inferred from direct assay
10036235 GOA
involved in cortical actin cytoskeleton organization IMP
IMP: Inferred from mutant phenotype
10913182 GOA
involved in endocytic recycling IDA
IDA: Inferred from direct assay
10036235 GOA
involved in positive regulation of actin filament polymerization IMP
IMP: Inferred from mutant phenotype
10036235 GOA
involved in positive regulation of mitotic cytokinetic process IMP
IMP: Inferred from mutant phenotype
17628206 GOA
involved in positive regulation of neuron projection development IDA
IDA: Inferred from direct assay
36250347 GOA
involved in positive regulation of protein secretion IMP
IMP: Inferred from mutant phenotype
27044754 GOA
involved in protein localization to cleavage furrow IMP
IMP: Inferred from mutant phenotype
16148947 GOA
involved in protein localization to endosome IMP
IMP: Inferred from mutant phenotype
21951725 GOA
involved in protein localization to plasma membrane IDA
IDA: Inferred from direct assay
37461827 GOA
involved in regulation of Rac protein signal transduction IDA
IDA: Inferred from direct assay
10036235 GOA
involved in regulation of filopodium assembly IDA
IDA: Inferred from direct assay
14978216 GOA
involved in ruffle assembly IDA
IDA: Inferred from direct assay
10036235 GOA
Cellular Component GO Annotation Evidence Reference Source
located in Flemming body IDA
IDA: Inferred from direct assay
23603394 GOA
located in cell cortex IDA
IDA: Inferred from direct assay
10913182 GOA
located in cleavage furrow IDA
IDA: Inferred from direct assay
23603394 GOA
is active in cleavage furrow IMP
IMP: Inferred from mutant phenotype
16148947 GOA
is active in cytosol IDA
IDA: Inferred from direct assay
32103017 GOA
located in cytosol IDA
IDA: Inferred from direct assay
10391955 GOA
located in endocytic vesicle IDA
IDA: Inferred from direct assay
19948740 GOA
located in endosome IDA
IDA: Inferred from direct assay
20682791 GOA
located in filopodium membrane IDA
IDA: Inferred from direct assay
14978216 GOA
located in membrane IDA
IDA: Inferred from direct assay
10391955 GOA
is active in midbody IMP
IMP: Inferred from mutant phenotype
16148947 GOA
is active in plasma membrane IDA
IDA: Inferred from direct assay
32103017 GOA
located in plasma membrane IDA
IDA: Inferred from direct assay
10036235 GOA
located in recycling endosome membrane IDA
IDA: Inferred from direct assay
10036235 GOA
located in ruffle IDA
IDA: Inferred from direct assay
9312003 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

ARF6 Protein Structure

Arf

Arf: ADP-ribosylation factor family (2 - 172)

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

ADP-ribosylation factor 6

Related Diseases

Diseases Alias
Cholera

Vibrio Cholerae Infection

Cholera - Vibrio Cholerae

Cholera Due To Vibrio Cholerae

Vibrio Cholerae

Cholera Syndrome

Asiatic Cholera

Epidemic Cholera

Deafness, Onychodystrophy, Osteodystrophy, Mental Retardation, And Seizures Syndrome

Door Syndrome

Doors Syndrome

Digitorenocerebral Syndrome

Autosomal Recessive Deafness-Onychodystrophy Syndrome

Deafness-Onychoosteodystrophy-Intellectual Disability Syndrome

DOORS

Drc Syndrome

Eronen Syndrome

Deafness-Onychodystrophy-Osteodystrophy-Intellectual Disability Syndrome

Brachydactyly Due To Absence Of Distal Phalanges

Deafness-Onychodystrophy-Osteodystrophy-Intellectual Disability-Seizures Syndrome

Deafness, Onychodystrophy, Osteodystrophy, And Mental Retardation Syndrome

Deafness-Oncychodystrophy-Osteodystrophy-Intellectual Disability Syndrome

Autosomal Recessive Hearing Loss-Onychodystrophy Syndrome

Hearing Loss-Onychodystrophy-Osteodystrophy-Intellectual Disability Syndrome

Hearing Loss-Onychodystrophy-Osteodystrophy-Intellectual Disability-Seizures Syndrome

Hearing Loss-Onychoosteodystrophy-Intellectual Disability Syndrome

Deafness, Onychodystrophy, Osteodystrophy, Intellectual Disability, And Seizures Syndrome

Deafness, Congenital Onychodystrophy, Recessive Form

Deafness, Onychodystrophy, Osteodystrophy, Mental Retardation Syndrome

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

Non-Syndromic X-Linked Intellectual Disability

X-Linked Non-Syndromic Intellectual Disability

Non-Specific X-Linked Mental Retardation

X-Linked Non-Specific Intellectual Disability

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
Bos taurus ARF6 VGNC VGNC:26061
Macaca mulatta ARF6 VGNC VGNC:84306
Mus musculus ARF6 MGD MGI:99435
Canis familiaris ARF6 VGNC VGNC:38031
Felis catus ARF6 VGNC VGNC:68044
Rattus norvegicus ARF6 RGD RGD:621279