TSPYL1: Difference between revisions

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)
End	116,279,930 bp
Gene location (Mouse)
Chr.	Chromosome 10 (mouse)
End	34,161,271 bp
RNA expression pattern
	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
	More reference expression data
Gene ontology
Molecular function	enzyme binding;
Cellular component	nucleus; nucleolus;
Biological process	nucleosome assembly; biological process;
	Sources:Amigo / QuickGO
Orthologs
	7259
	22110
	ENSG00000189241
	ENSMUSG00000047514
	Q9H0U9
	O88852
	NM_003309
	NM_009433
	NP_003300
	NP_033459
	Wikidata
View/Edit Human	View/Edit Mouse

Browse history interactively

← Previous edit Next edit →

Content deleted Content added

VisualWikitext

Inline

Revision as of 17:55, 11 October 2020

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

References

^ ^a ^b ^c GRCh38: Ensembl release 89: ENSG00000189241 – Ensembl, May 2017
^ ^a ^b ^c GRCm38: Ensembl release 89: ENSMUSG00000047514 – Ensembl, May 2017
^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
^ 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.
^ "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. 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.

This article on a gene on human chromosome 6 is a stub. You can help Wikipedia by expanding it.

[refGRCh38Ensembl-1] GRCh38: Ensembl release 89: ENSG00000189241 – Ensembl, May 2017

[refGRCm38Ensembl-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.

[pmid9730615-5] 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.

[entrez-6] "Entrez Gene: TSPYL1 TSPY-like 1".

[1]

[2]

[3]

[4]

[5]

[6]

@@ Line 1: / Line 1: @@
 {{Infobox_gene}}
-'''Testis-specific Y-encoded-like protein 1''' is a [[protein]] that in humans is encoded by the ''TSPYL1'' [[gene]].<ref name="pmid9730615">{{cite journal | vauthors = Vogel T, Dittrich O, Mehraein Y, Dechend F, Schnieders F, Schmidtke J | title = Murine and human TSPYL genes: novel members of the TSPY-SET-NAP1L1 family | journal = Cytogenet Cell Genet | volume = 81 | issue = 3–4 | pages = 265–70 |date=Oct 1998 | pmid = 9730615 | pmc =  | doi =10.1159/000015042  }}</ref><ref name="entrez">{{cite web | title = Entrez Gene: TSPYL1 TSPY-like 1| url = https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=7259| accessdate = }}</ref>
+'''Testis-specific Y-encoded-like protein 1''' is a [[protein]] that in humans is encoded by the ''TSPYL1'' [[gene]].<ref name="pmid9730615">{{cite journal | vauthors = Vogel T, Dittrich O, Mehraein Y, Dechend F, Schnieders F, Schmidtke J | title = Murine and human TSPYL genes: novel members of the TSPY-SET-NAP1L1 family | journal = Cytogenet Cell Genet | volume = 81 | issue = 3–4 | pages = 265–70 |date=Oct 1998 | pmid = 9730615 | pmc =  | doi =10.1159/000015042  | s2cid = 46829106 }}</ref><ref name="entrez">{{cite web | title = Entrez Gene: TSPYL1 TSPY-like 1| url = https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=7259| accessdate = }}</ref>
@@ Line 14: / Line 14: @@
 *{{cite journal   |vauthors=Strausberg RL, Feingold EA, Grouse LH, etal |title=Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=99 |issue= 26 |pages= 16899–903 |year= 2003 |pmid= 12477932 |doi= 10.1073/pnas.242603899  | pmc=139241 }}
 *{{cite journal   |vauthors=Ota T, Suzuki Y, Nishikawa T, etal |title=Complete sequencing and characterization of 21,243 full-length human cDNAs |journal=Nat. Genet. |volume=36 |issue= 1 |pages= 40–5 |year= 2004 |pmid= 14702039 |doi= 10.1038/ng1285 |doi-access= free }}
-*{{cite journal   |vauthors=Puffenberger EG, Hu-Lince D, Parod JM, etal |title=Mapping of sudden infant death with dysgenesis of the testes syndrome (SIDDT) by a SNP genome scan and identification of TSPYL loss of function |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=101 |issue= 32 |pages= 11689–94 |year= 2004 |pmid= 15273283 |doi= 10.1073/pnas.0401194101  | pmc=511011 }}
+*{{cite journal   |vauthors=Puffenberger EG, Hu-Lince D, Parod JM, etal |title=Mapping of sudden infant death with dysgenesis of the testes syndrome (SIDDT) by a SNP genome scan and identification of TSPYL loss of function |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=101 |issue= 32 |pages= 11689–94 |year= 2004 |pmid= 15273283 |doi= 10.1073/pnas.0401194101  | pmc=511011 |bibcode=2004PNAS..10111689P }}
 *{{cite journal   |vauthors=Gerhard DS, Wagner L, Feingold EA, etal |title=The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC) |journal=Genome Res. |volume=14 |issue= 10B |pages= 2121–7 |year= 2004 |pmid= 15489334 |doi= 10.1101/gr.2596504  | pmc=528928 }}
 *{{cite journal   |vauthors=de Andrade TG, Peterson KR, Cunha AF, etal |title=Identification of novel candidate genes for globin regulation in erythroid cells containing large deletions of the human beta-globin gene cluster |journal=Blood Cells Mol. Dis. |volume=37 |issue= 2 |pages= 82–90 |year= 2006 |pmid= 16952470 |doi= 10.1016/j.bcmd.2006.07.003 }}

Revision as of 17:55, 11 October 2020

References

Further reading