TCF19

Transcription factor 19 is a protein that in humans is encoded by the TCF19 gene.[5][6][7]

TCF19
Identifiers
Aliases	TCF19, SC1, TCF-19, transcription factor 19
External IDs	OMIM: 600912 MGI: 103180 HomoloGene: 5156 GeneCards: TCF19
Gene location (Human) Chr. Chromosome 6 (human)[1] Band 6p21.33 Start 31,158,547 bp[1] End 31,167,159 bp[1]
Gene location (Mouse) Chr. Chromosome 17 (mouse)[2] Band 17|17 B1 Start 35,512,734 bp[2] End 35,516,824 bp[2]
Gene ontology Molecular function • GO:0001131, GO:0001151, GO:0001130, GO:0001204 DNA-binding transcription factor activity • metal ion binding • GO:0001948 protein binding Cellular component • cell nucleus Biological process • transcription, DNA-templated • regulation of transcription from RNA polymerase II promoter • cellular proliferation • regulation of transcription, DNA-templated Sources:Amigo / QuickGO
Orthologs
Species	Human	Mouse
Entrez	6941	106795
Ensembl	ENSG00000233890 ENSG00000224472 ENSG00000137310 ENSG00000224941 ENSG00000234674 ENSG00000206455 ENSG00000224379	ENSMUSG00000050410
UniProt	Q9Y242	Q99KJ5
RefSeq (mRNA)	NM_001077511 NM_007109 NM_001318908	NM_001163763 NM_001163764 NM_025674
RefSeq (protein)	NP_001070979 NP_001305837 NP_009040	NP_001157235 NP_001157236 NP_079950
Location (UCSC)	Chr 6: 31.16 – 31.17 Mb	Chr 17: 35.51 – 35.52 Mb
PubMed search	[3]	[4]
Wikidata
View/Edit Human View/Edit Mouse

References

1. ENSG00000224472, ENSG00000137310, ENSG00000224941, ENSG00000234674, ENSG00000206455, ENSG00000224379 GRCh38: Ensembl release 89: ENSG00000233890, ENSG00000224472, ENSG00000137310, ENSG00000224941, ENSG00000234674, ENSG00000206455, ENSG00000224379 - Ensembl, May 2017
2. GRCm38: Ensembl release 89: ENSMUSG00000050410 - Ensembl, May 2017
3. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
4. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
5. Ku DH, Chang CD, Koniecki J, Cannizzaro LA, Boghosian-Sell L, Alder H, Baserga R (Sep 1991). "A new growth-regulated complementary DNA with the sequence of a putative trans-activating factor". Cell Growth Differ. 2 (4): 179–86. PMID 1868030.
6. Krishnan BR, Jamry I, Chaplin DD (Apr 1996). "Feature mapping of the HLA class I region: localization of the POU5F1 and TCF19 genes". Genomics. 30 (1): 53–8. doi:10.1006/geno.1995.0008. PMID 8595903.
7. "Entrez Gene: TCF19 transcription factor 19 (SC1)".

Further reading

• Teraoka Y, Naruse TK, Oka A, et al. (2000). "Genetic polymorphisms in the cell growth regulated gene, SC1 telomeric of the HLA-C gene and lack of association of psoriasis vulgaris". Tissue Antigens. 55 (3): 206–11. doi:10.1034/j.1399-0039.2000.550303.x. PMID 10777095.
• Strausberg RL, Feingold EA, Grouse LH, et al. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. doi:10.1073/pnas.242603899. PMC 139241. PMID 12477932.
• Mungall AJ, Palmer SA, Sims SK, et al. (2003). "The DNA sequence and analysis of human chromosome 6". Nature. 425 (6960): 805–11. Bibcode:2003Natur.425..805M. doi:10.1038/nature02055. PMID 14574404.
• Suzuki Y, Yamashita R, Shirota M, et al. (2004). "Sequence Comparison of Human and Mouse Genes Reveals a Homologous Block Structure in the Promoter Regions". Genome Res. 14 (9): 1711–8. doi:10.1101/gr.2435604. PMC 515316. PMID 15342556.
• Gerhard DS, Wagner L, Feingold EA, et al. (2004). "The Status, Quality, and Expansion of the NIH Full-Length cDNA Project: The Mammalian Gene Collection (MGC)". Genome Res. 14 (10B): 2121–7. doi:10.1101/gr.2596504. PMC 528928. PMID 15489334.
• Kimura K, Wakamatsu A, Suzuki Y, et al. (2006). "Diversification of transcriptional modulation: Large-scale identification and characterization of putative alternative promoters of human genes". Genome Res. 16 (1): 55–65. doi:10.1101/gr.4039406. PMC 1356129. PMID 16344560.
• Shiina T, Ota M, Shimizu S, et al. (2006). "Rapid Evolution of Major Histocompatibility Complex Class I Genes in Primates Generates New Disease Alleles in Humans via Hitchhiking Diversity". Genetics. 173 (3): 1555–70. doi:10.1534/genetics.106.057034. PMC 1526686. PMID 16702430.