SOX12 - SRY-box transcription factor 12 Gene

Also Known as SOX22

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 6666

About SOX12

Cytogenetic location: 20p13 Genomic coordinates (GRCh38): 20:325,552-330,224 (from NCBI)

This gene has 1 transcript (splice variant), 265 orthologues and 20 paralogues.

Summary

Members of the SOX family of transcription factors are characterized by the presence of a DNA-binding high mobility group (HMG) domain, homologous to the HMG box of sex-determining region Y (SRY). Forming a subgroup of the HMG domain superfamily, SOX proteins have been implicated in cell fate decisions in a diverse range of developmental processes. SOX transcription factors have diverse tissue-specific expression patterns during early development and have been proposed to act as target-specific transcription factors and/or as chromatin structure regulatory elements. The protein encoded by this gene was identified as a SOX family member based on conserved domains, and its expression in various tissues suggests a role in both differentiation and maintenance of several cell types. [provided by RefSeq, Jan 2013]

SOX12 Products (1)

mRNA Protein Name
NM_006943.4 NP_008874.2 transcription factor SOX-12
Molecular Function GO Annotation Evidence References 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

SOX12 Protein Structure

HMG_box

HMG_box: HMG (high mobility group) box (40 - 108)

  • 0
  • 100
  • 200
  • 300
  • 315 a.a.
Protein Preferred Names Protein Names

transcription factor SOX-12

  • SOX-22 protein

Related Diseases

Diseases Alias
Acromesomelic Dysplasia 2a
  • Chondrodysplasia, Grebe Type

  • Acromesomelic Dysplasia, Grebe Type

  • Grebe Chondrodysplasia

  • Amdg

  • Grebe Syndrome

  • AMD2A

  • Grebe Dysplasia

  • Achondrogenesis, Brazilian

  • Achondrogenesis, Type Ii, Formerly

  • Acromesomelic Dysplasia-2a

  • Achondrogenesis Type Ii

  • Brazilian Achondrogenesis

  • Acromesomelic Chondrodysplasia, Grebe Type

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
Mus musculus SOX12 MGD MGI:98360
Canis familiaris SOX12 VGNC VGNC:46673
Rattus norvegicus SOX12 RGD RGD:1586313
Bos taurus SOX12 VGNC VGNC:106945
Others SOX12 NCBI