TSPYL1

From Wikipedia, the free encyclopedia

TSPY-like 1

Identifiers

TSPYL1; SIDDT; TSPYL

External IDs

OMIM: 604714 MGI: 1298395 HomoloGene: 22522

Gene ontology
Molecular Function:	• molecular_function
Cellular Component:	• cellular_component • intracellular • nucleus
Biological Process:	• nucleosome assembly • biological_process

RNA expression pattern

More reference expression data

Orthologs

Human

Mouse

Refseq

NM_003309 (mRNA)
NP_003300 (protein)

NM_009433 (mRNA)
NP_033459 (protein)

Location

Chr 6: 116.7 - 116.71 Mb

Chr 10: 33.97 - 33.97 Mb

Pubmed search

[1]

[2]

TSPY-like 1, also known as TSPYL1, is a human gene.^[1]

[edit] References

^ Entrez Gene: TSPYL1 TSPY-like 1.

[edit] Further reading

Vogel T, Dittrich O, Mehraein Y, et al. (1998). "Murine and human TSPYL genes: novel members of the TSPY-SET-NAP1L1 family.". Cytogenet. Cell Genet. 81 (3-4): 265-70. PMID 9730615.
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.154701. 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. 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. 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. 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. doi:10.1073/pnas.0401194101. 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. 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.