SPATC1L

SPATC1L
Identifiers
Aliases	SPATC1L, C21orf56, spermatogenesis and centriole associated 1-like, spermatogenesis and centriole associated 1 like
External IDs	OMIM: 612412; MGI: 1923823; HomoloGene: 75292; GeneCards: SPATC1L; OMA:SPATC1L - orthologs
Gene location (Human)
Chr.	Chromosome 21 (human)
End	46,184,476 bp
Gene location (Mouse)
Chr.	Chromosome 10 (mouse)
End	76,406,035 bp
RNA expression pattern
	Top expressed in
	right testis; ; left testis; ; left adrenal cortex; ; prostate; ; right adrenal cortex; ; putamen; ; temporal lobe; ; amygdala; ; nucleus accumbens; ; hippocampus proper;
	Top expressed in
	seminiferous tubule; ; spermatid; ; parasympathetic nervous system; ; thyroid gland; ; pharynx; ; tongue; ; spermatocyte; ; embryo; ; submandibular gland; ; right kidney;
	More reference expression data
	n/a
Gene ontology
Molecular function	protein binding; molecular function;
Cellular component	centrosome; cellular component;
Biological process	biological process;
	Sources:Amigo / QuickGO
Orthologs
	84221
	76573
	ENSG00000160284; ENSG00000274679
	ENSMUSG00000009115
	Q9H0A9
	Q9D9W0
	NM_001142854; NM_032261
	NM_029661; NM_001359186
	NP_001136326; NP_115637
	NP_083937; NP_001346115
	Wikidata
View/Edit Human	View/Edit Mouse

SPATC1L is a protein that in humans is encoded by the SPATC1L gene.^[5]

References

^ ^a ^b ^c ENSG00000274679 GRCh38: Ensembl release 89: ENSG00000160284, ENSG00000274679 – Ensembl, May 2017
^ ^a ^b ^c GRCm38: Ensembl release 89: ENSMUSG00000009115 – 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.
^ "Entrez Gene: C21orf56 chromosome 21 open reading frame 56".

External links

Human SPATC1L genome location and SPATC1L gene details page in the UCSC Genome Browser.

Mehrle A, Rosenfelder H, Schupp I, et al. (2006). "The LIFEdb database in 2006". Nucleic Acids Res. 34 (Database issue): D415–8. doi:10.1093/nar/gkj139. PMC 1347501. PMID 16381901.
Wiemann S, Arlt D, Huber W, et al. (2004). "From ORFeome to biology: a functional genomics pipeline". Genome Res. 14 (10B): 2136–44. doi:10.1101/gr.2576704. PMC 528930. PMID 15489336.
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.
Lehner B, Sanderson CM (2004). "A protein interaction framework for human mRNA degradation". Genome Res. 14 (7): 1315–23. doi:10.1101/gr.2122004. PMC 442147. PMID 15231747.
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.
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.
Hartley JL, Temple GF, Brasch MA (2001). "DNA cloning using in vitro site-specific recombination". Genome Res. 10 (11): 1788–95. doi:10.1101/gr.143000. PMC 310948. PMID 11076863.
Hattori M, Fujiyama A, Taylor TD, et al. (2000). "The DNA sequence of human chromosome 21". Nature. 405 (6784): 311–9. Bibcode:2000Natur.405..311H. doi:10.1038/35012518. PMID 10830953.

This article on a gene on human chromosome 21 is a stub. You can help Wikipedia by expanding it.

[refGRCh38Ensembl-1] ENSG00000274679 GRCh38: Ensembl release 89: ENSG00000160284, ENSG00000274679 – Ensembl, May 2017

[refGRCm38Ensembl-2] GRCm38: Ensembl release 89: ENSMUSG00000009115 – 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.

[entrez-5] "Entrez Gene: C21orf56 chromosome 21 open reading frame 56".

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References

External links

Further reading