TSPYL1

Identifiers

TSPYL1, TSPYL, TSPY-like 1, TSPY like 1

External IDs

MGI: 1298395 HomoloGene: 22522 GeneCards: TSPYL1

Gene location (Human)

Chr.	Chromosome 6 (human)^[1]

Band	No data available	Start	116,276,578 bp^[1]
Band	No data available	End	116,279,903 bp^[1]

Gene location (Mouse)

Chr.	Chromosome 10 (mouse)^[2]

Band	No data available	Start	34,282,190 bp^[2]
Band	No data available	End	34,285,275 bp^[2]

RNA expression pattern

More reference expression data

Gene ontology
Molecular function	• enzyme binding
Cellular component	• nucleus • nucleolus
Biological process	• nucleosome assembly
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: 116.28 – 116.28 Mb

Chr 6: 34.28 – 34.29 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 2 3 GRCh38: Ensembl release 89: ENSG00000189241 - Ensembl, May 2017
1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000047514 - Ensembl, May 2017
↑ "Human PubMed Reference:".
↑ "Mouse PubMed Reference:".
↑ 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. PMID 9730615. doi:10.1159/000015042.
↑ "Entrez Gene: TSPYL1 TSPY-like 1".

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. PMC 311072 . PMID 11230166. doi:10.1101/gr.GR1547R.
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. PMC 1083732 . PMID 11256614. doi:10.1093/embo-reports/kvd058.
Scherl A, Couté Y, Déon C, et al. (2003). "Functional proteomic analysis of human nucleolus". Mol. Biol. Cell. 13 (11): 4100–9. PMC 133617 . PMID 12429849. doi:10.1091/mbc.E02-05-0271.
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. PMC 139241 . PMID 12477932. doi:10.1073/pnas.242603899.
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. PMID 14702039. doi:10.1038/ng1285.
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. PMC 511011 . PMID 15273283. doi:10.1073/pnas.0401194101.
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. PMC 528928 . PMID 15489334. doi:10.1101/gr.2596504.
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. PMID 16952470. doi:10.1016/j.bcmd.2006.07.003.

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TSPYL1

References

Further reading