SOX5

SOX5
Identifiers
Aliases SOX5, L-L-SOX5B, L-SOX5F, LAMSHF, SRY-box 5
External IDs MGI: 98367 HomoloGene: 21378 GeneCards: SOX5
Genetically Related Diseases
azoospermia, systemic scleroderma[1]
RNA expression pattern
More reference expression data
Orthologs
Species Human Mouse
Entrez

6660

20678

Ensembl

ENSG00000134532

ENSMUSG00000041540

UniProt

P35711

P35710

RefSeq (mRNA)

NM_001261414
NM_001261415
NM_006940
NM_152989
NM_178010

NM_001113559
NM_001243163
NM_011444

RefSeq (protein)

NP_001248343.1
NP_001248344.1
NP_008871.3
NP_694534.1
NP_821078.1

NP_001230092.1

Location (UCSC) Chr 12: 23.53 – 23.95 Mb Chr 6: 143.83 – 144.78 Mb
PubMed search [2] [3]
Wikidata
View/Edit HumanView/Edit Mouse

Transcription factor SOX-5 is a protein that in humans is encoded by the SOX5 gene.[4][5]

Function

This gene encodes a member of the SOX (SRY-related HMG-box) family of transcription factors involved in the regulation of embryonic development and in the determination of the cell fate. The encoded protein may act as a transcriptional regulator after forming a protein complex with other proteins. The encoded protein may play a role in chondrogenesis. A pseudogene of this gene is located on chromosome 8. Multiple transcript variants encoding distinct isoforms have been identified for this gene.[5]

See also

References

  1. "Diseases that are genetically associated with SOX5 view/edit references on wikidata".
  2. "Human PubMed Reference:".
  3. "Mouse PubMed Reference:".
  4. Wunderle VM, Critcher R, Ashworth A, Goodfellow PN (Sep 1996). "Cloning and characterization of SOX5, a new member of the human SOX gene family". Genomics. 36 (2): 354–8. doi:10.1006/geno.1996.0474. PMID 8812465.
  5. 1 2 "Entrez Gene: SOX5 SRY (sex determining region Y)-box 5".

Further reading

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