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
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
	prostate; ; putamen; ; temporal lobe; ; amygdala; ; nucleus accumbens; ; hippocampus proper; ; superior frontal gyrus; ; caudate nucleus; ; hypothalamus; ; dorsolateral prefrontal cortex;
	Top expressed in
	seminiferous tubule; ; spermatid; ; parasympathetic nervous system; ; thyroid gland; ; pharynx; ; tongue; ; spermatocyte; ; submandibular gland; ; proximal tubule; ; spinal ganglia;
	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

Last updated December 30, 2022

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

Related Research Articles

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References

1 2 3 ENSG00000274679 GRCh38: Ensembl release 89: ENSG00000160284, ENSG00000274679 - Ensembl, May 2017
1 2 3 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.

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[refGRCh38Ensembl-1] 1 2 3 ENSG00000274679 GRCh38: Ensembl release 89: ENSG00000160284, ENSG00000274679 - Ensembl, May 2017

[refGRCm38Ensembl-2] 1 2 3 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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SPATC1L

Contents

Related Research Articles

References

External links

Further reading