SOX9
位於17號人類染色體的基因
SOX9(英語:Transcription factor SOX-9)是一種轉錄因子,由人類基因Sox9編碼,是塞爾托利氏細胞等細胞的標誌物[5][6]。
相互作用
編輯參考文獻
編輯- ^ 1.0 1.1 1.2 GRCh38: Ensembl release 89: ENSG00000125398 - Ensembl, May 2017
- ^ 2.0 2.1 2.2 GRCm38: Ensembl release 89: ENSMUSG00000000567 - Ensembl, May 2017
- ^ Human PubMed Reference:. National Center for Biotechnology Information, U.S. National Library of Medicine.
- ^ Mouse PubMed Reference:. National Center for Biotechnology Information, U.S. National Library of Medicine.
- ^ Tommerup N, Schempp W, Meinecke P, Pedersen S, Bolund L, Brandt C, et al. Assignment of an autosomal sex reversal locus (SRA1) and campomelic dysplasia (CMPD1) to 17q24.3-q25.1. Nature Genetics. June 1993, 4 (2): 170–4. PMID 8348155. S2CID 12263655. doi:10.1038/ng0693-170.
- ^ Entrez Gene: SOX9 SRY (sex determining region Y)-box 9 (campomelic dysplasia, autosomal sex-reversal). [2021-06-01]. (原始內容存檔於2010-03-07).
- ^ Zhou R, Bonneaud N, Yuan CX, de Santa Barbara P, Boizet B, Schomber T, et al. SOX9 interacts with a component of the human thyroid hormone receptor-associated protein complex. Nucleic Acids Research. July 2002, 30 (14): 3245–52. PMC 135763 . PMID 12136106. doi:10.1093/nar/gkf443.
- ^ Huang W, Lu N, Eberspaecher H, De Crombrugghe B. A new long form of c-Maf cooperates with Sox9 to activate the type II collagen gene. The Journal of Biological Chemistry. December 2002, 277 (52): 50668–75. PMID 12381733. doi:10.1074/jbc.M206544200 .
外部連結
編輯- 醫學主題詞表(MeSH):SOX9+protein,+human
- Template:UCSC genome browser
- Template:UCSC gene details
- PDB中UniProt可用的所有結構資訊之概述:P48436 (Human Transcription factor SOX-9) 在PDBe-KB。
- PDB中UniProt可用的所有結構資訊之概述:Q04887 (Mouse Transcription factor SOX-9) 在PDBe-KB。