TSPYL1

TSPYL1
Identifiers
Aliases	TSPYL1 , TSPYL, TSPY-like 1, TSPY like 1
External IDs	OMIM: 604714; MGI: 1298395; HomoloGene: 22522; GeneCards: TSPYL1; OMA:TSPYL1 - orthologs
Gene location (Human) Chr. Chromosome 6 (human) [1] Band 6q22.1 Start 116,267,760 bp [1] End 116,279,930 bp [1]
Gene location (Mouse) Chr. Chromosome 10 (mouse) [2] Band 10|10 B1 Start 34,158,186 bp [2] End 34,161,271 bp [2]
RNA expression pattern Bgee Human Mouse (ortholog) Top expressed in germinal epithelium lateral nuclear group of thalamus pons Brodmann area 23 pars compacta seminal vesicula external globus pallidus superior vestibular nucleus parietal lobe Skeletal muscle tissue of rectus abdominis Top expressed in ventral tegmental area habenula dorsomedial hypothalamic nucleus pontine nuclei lateral hypothalamus globus pallidus Gonadal ridge paraventricular nucleus of hypothalamus median eminence arcuate nucleus More reference expression data BioGPS More reference expression data
Gene ontology Molecular function enzyme binding Cellular component nucleus nucleolus Biological process nucleosome assembly biological process Sources:Amigo / QuickGO
Orthologs Species Human Mouse Entrez 7259 22110 Ensembl ENSG00000189241 ENSMUSG00000047514 UniProt Q9H0U9 O88852 RefSeq (mRNA) NM_003309 NM_009433 RefSeq (protein) NP_003300 NP_033459 Location (UCSC) Chr 6: 116.27 – 116.28 Mb Chr 10: 34.16 – 34.16 Mb PubMed search [3] [4]
Wikidata
View/Edit Human View/Edit Mouse

Testis-specific Y-encoded-like protein 1 is a protein that in humans is encoded by the TSPYL1 gene. ^{[5] [6]}

References

1. GRCh38: Ensembl release 89: ENSG00000189241 – Ensembl, May 2017
2. GRCm38: Ensembl release 89: ENSMUSG00000047514 – 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. Vogel T, Dittrich O, Mehraein Y, Dechend F, Schnieders F, Schmidtke J (Oct 1998). "Murine and human TSPYL genes: novel members of the TSPY-SET-NAP1L1 family". Cytogenet Cell Genet. 81 (3–4): 265–70. doi:10.1159/000015042. PMID   9730615. S2CID   46829106.
6. "Entrez Gene: TSPYL1 TSPY-like 1".

Further reading

• 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. Bibcode:2002PNAS...9916899M. 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.