SOX11

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

Transcription factor SOX-11 is a protein that in humans is encoded by the SOX11 gene.[5][6][7]

AliasesSOX11, MRD27, SRY-box 11, CSS9, SRY-box transcription factor 11
End5,701,385 bp[1]
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SOX11
Identifiers
AliasesSOX11, MRD27, SRY-box 11, CSS9, SRY-box transcription factor 11
External IDsOMIM: 600898; MGI: 98359; HomoloGene: 37733; GeneCards: SOX11; OMA:SOX11 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_003108

NM_009234

RefSeq (protein)

NP_003099

NP_033260

Location (UCSC)Chr 2: 5.69 – 5.7 MbChr 12: 27.38 – 27.39 Mb
PubMed search[3][4]
Wikidata
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Function

This intronless gene encodes a member of the group C SOX (SRY-related HMG-box) transcription factor family 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 protein may function in the developing nervous system and play a role in tumorigenesis and adult neurogenesis.[7][8] Tuj1 and Tead2 are suggested as direct target of Sox11.[9][10][11]

Clinical aspect

Lymphocyte staining for SOX11 immunohistochemistry indicates mantle cell lymphoma (cyclin D1 positive and negative) rather than other mature lymphoid neoplasms or normal lymphocytes.[12]

Mutations in SOX11 are associated with Coffin–Siris syndrome[13] and mantle cell lymphoma.[14]

See also

References

Further reading

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