TSPYL1

TSPYL1
Identifikatori
Aliasi	TSPYL1
Vanjski ID-jevi	OMIM: 604714 MGI: 1298395 HomoloGene: 22522 GeneCards: TSPYL1
Lokacija gena (čovjek) Hrom. Hromosom 6 (čovjek) Bend 6q22.1 Početak 116,267,760 bp Kraj 116,279,930 bp
Lokacija gena (miš) Hrom. Hromosom 10 (miš) Bend 10|10 B1 Početak 34,158,186 bp Kraj 34,161,271 bp
Obrazac RNK ekspresije Više referentnih podataka o ekspresiji
Ontologija gena Molekularna funkcija • vezivanje enzima Ćelijska komponenta • jedro • Jedarce Biološki proces • nucleosome assembly • GO:0022610 biološki proces Izvori:Amigo / QuickGO
Ortolozi
Vrste	Čovjek	Miš
Entrez	7259	22110
Ensembl	ENSG00000189241	ENSMUSG00000047514
UniProt	Q9H0U9	O88852
RefSeq (mRNK)	NM_003309	NM_009433
RefSeq (bjelančevina)	NP_003300	NP_033459
Lokacija (UCSC)	Chr 6: 116.27 – 116.28 Mb	Chr 10: 34.16 – 34.16 Mb
PubMed pretraga
Wikipodaci
Pogledaj/uredi – čovjek Pogledaj/uredi – miš

Testis-specifični Y-kodiranoliki protein 1 je protein koji je kod ljudi kodiran genom TSPYL1.

Dopunska literatura

• Wiemann S, Weil B, Wellenreuther R, et al. (2001). "Toward a catalog of human genes and proteins: sequencing and analysis of 500 novel complete protein coding human cDNAs". Genome Res. 11 (3): 422–35. doi:10.1101/gr.GR1547R. PMC 311072. PMID 11230166.
• Simpson JC, Wellenreuther R, Poustka A, et al. (2001). "Systematic subcellular localization of novel proteins identified by large-scale cDNA sequencing". EMBO Rep. 1 (3): 287–92. doi:10.1093/embo-reports/kvd058. PMC 1083732. PMID 11256614.
• Scherl A, Couté Y, Déon C, et al. (2003). "Functional proteomic analysis of human nucleolus". Mol. Biol. Cell. 13 (11): 4100–9. doi:10.1091/mbc.E02-05-0271. PMC 133617. PMID 12429849.
• 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.
• Ota T, Suzuki Y, Nishikawa T, et al. (2004). "Complete sequencing and characterization of 21,243 full-length human cDNAs". Nat. Genet. 36 (1): 40–5. doi:10.1038/ng1285. PMID 14702039.
• Puffenberger EG, Hu-Lince D, Parod JM, et al. (2004). "Mapping of sudden infant death with dysgenesis of the testes syndrome (SIDDT) by a SNP genome scan and identification of TSPYL loss of function". Proc. Natl. Acad. Sci. U.S.A. 101 (32): 11689–94. Bibcode:2004PNAS..10111689P. doi:10.1073/pnas.0401194101. PMC 511011. PMID 15273283.
• 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.
• de Andrade TG, Peterson KR, Cunha AF, et al. (2006). "Identification of novel candidate genes for globin regulation in erythroid cells containing large deletions of the human beta-globin gene cluster". Blood Cells Mol. Dis. 37 (2): 82–90. doi:10.1016/j.bcmd.2006.07.003. PMID 16952470.