1. Gene
  2. DOCK4 - dedicator of cytokinesis 4 Gene

DOCK4 - dedicator of cytokinesis 4 Gene

Homo sapiens
Gene ID: 9732 | Gene type: protein coding

About DOCK4

Cytogenetic location: 7q31.1 Genomic coordinates (GRCh38): 7:111,726,110-112,206,399 (from NCBI)

This gene has 18 transcripts (splice variants), 228 orthologues and 10 paralogues. Broad expression in lung (RPKM 9.6), brain (RPKM 9.0) and 23 other tissues.

Summary

This gene is a member of the dedicator of cytokinesis (DOCK) family and encodes a protein with a DHR-1 (CZH-1) domain, a DHR-2 (CZH-2) domain and an SH3 domain. This membrane-associated, cytoplasmic protein functions as a guanine nucleotide exchange factor and is involved in regulation of adherens junctions between cells. Mutations in this gene have been associated with ovarian, prostate, glioma, and colorectal cancers. Alternatively spliced variants which encode different protein isoforms have been described, but only one has been fully characterized. [provided by RefSeq, Jul 2008]

DOCK4 Products(2)

mRNA Protein Name
NM_001363540.2 NP_001350469.1 dedicator of cytokinesis protein 4 isoform 2
NM_014705.4 NP_055520.3 dedicator of cytokinesis protein 4 isoform 1

DOCK4 Protein Structure

SH3_2

SH3_2: Variant SH3 domain (10 - 62)

DOCK-C2

DOCK-C2: C2 domain in Dock180 and Zizimin proteins (396 - 583)

DHR-2

DHR-2: Dock homology region 2 (1406 - 1587)

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  • 1966 a.a.
Protein Preferred Names Protein Names

dedicator of cytokinesis protein 4

Related Diseases

Diseases Alias
Placenta Accreta
Autism

Autistic Disorder

Autism Susceptibility 1

Childhood Autism

Autistic Disorder Of Childhood Onset

Infantile Autism

Kanner'S Syndrome

Autistic

Deafness, Autosomal Recessive 14

DFNB14

Autosomal Recessive Nonsyndromic Deafness 14

Autosomal Recessive Deafness 14

Dyslexia
Reading Disorder

Specific Reading Disorder

Reading

Dyslexia

Developmental Reading Disorder

Deafness, Autosomal Recessive 17

DFNB17

Autosomal Recessive Nonsyndromic Deafness 17

Autosomal Recessive Deafness 17

Learning Disability

Learning Disabilities

Learning Disorders

Academic Skill Disorder

Learning Disorder

Specific Language Impairment

Language Impairment, Specific

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
Macaca mulatta DOCK4 VGNC VGNC:71866
Canis familiaris DOCK4 VGNC VGNC:40048
Rattus norvegicus DOCK4 RGD RGD:1561724
Mus musculus DOCK4 MGD MGI:1918006
Bos taurus DOCK4 VGNC VGNC:28158
Felis catus DOCK4 VGNC VGNC:61573