1. Gene
  2. SIX4 - SIX homeobox 4 Gene

SIX4 - SIX homeobox 4 Gene

Homo sapiens

Also known as AREC3

Gene ID: 51804 | Gene type: protein coding

About SIX4

Cytogenetic location: 14q23.1 Genomic coordinates (GRCh38): 14:60,709,539-60,724,351 (from NCBI)

This gene has 3 transcripts (splice variants), 225 orthologues and 6 paralogues. Broad expression in prostate (RPKM 2.0), salivary gland (RPKM 1.8) and 16 other tissues.

Summary

This gene encodes a member of the homeobox family, subfamily SIX. The drosophila homolog is a nuclear homeoprotein required for eye development. Studies in mouse show that this gene product functions as a transcription factor, and may have a role in the differentiation or maturation of neuronal cells. [provided by RefSeq, May 2010]

SIX4 Products(1)

mRNA Protein Name
NM_017420.5 NP_059116.3 homeobox protein SIX4
Gene Ontology
  • Molecular Function
Molecular Function GO Annotation Evidence Reference Source
enables sequence-specific double-stranded DNA binding IDA
IDA: Inferred from direct assay
28473536 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

SIX4 Protein Structure

Homeobox

Homeobox: Homeobox domain (230 - 279)

  • 0
  • 200
  • 400
  • 600
  • 781 a.a.
Protein Preferred Names Protein Names

homeobox protein SIX4

sine oculis homeobox homolog 4

Related Diseases

Diseases Alias
Branchiootic Syndrome

Bo Syndrome

Branchiootic Dysplasia

Bor

Bo Syndrome 1

Bos1

Branchiootic Syndrome 1

Bardet-Biedl Syndrome 8

BBS8

Bardet-Biedl Syndrome, Type 8

Branchiootorenal Syndrome

Branchio-Oto-Renal Syndrome

Bor Syndrome

Branchiootorenal Dysplasia

Melnick-Fraser Syndrome

Branchiootorenal Spectrum Disorders

Branchio-Otorenal Dysplasia

Branchio Oto Renal Syndrome

Branchiootorenal/Branchiootic Syndrome

Bo Syndrome

Bor

Bos

Branchio-Otorenal Syndrome

Branchiootic Syndrome

Branchiootorenal Syndrome

Branchiootic Syndrome 1

Paralytic Squint

Paralytic Strabismus

Incomitant Dissociation

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 SIX4 VGNC VGNC:46192
Mus musculus SIX4 MGD MGI:106034
Felis catus SIX4 VGNC VGNC:80845
Macaca mulatta SIX4 VGNC VGNC:99240
Bos taurus SIX4 VGNC VGNC:109396
Rattus norvegicus SIX4 RGD RGD:1306726