SPATC1L

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

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)[1] Band 21q22.3 Start 46,161,148 bp[1] End 46,184,476 bp[1]
Gene location (Mouse) Chr. Chromosome 10 (mouse)[2] Band 10|10 C1 Start 76,562,272 bp[2] End 76,570,201 bp[2]
Gene ontology Molecular function • GO:0001948 protein binding • molecular function Cellular component • centrosome • cellular component Biological process • biological process Sources:Amigo / QuickGO
Orthologs
Species	Human	Mouse
Entrez	84221	76573
Ensembl	ENSG00000160284 ENSG00000274679	ENSMUSG00000009115
UniProt	Q9H0A9	Q9D9W0
RefSeq (mRNA)	NM_001142854 NM_032261	NM_029661 NM_001359186
RefSeq (protein)	NP_001136326 NP_115637	NP_083937 NP_001346115
Location (UCSC)	Chr 21: 46.16 – 46.18 Mb	Chr 10: 76.56 – 76.57 Mb
PubMed search	[3]	[4]
Wikidata
View/Edit Human View/Edit Mouse

References

1. ENSG00000274679 GRCh38: Ensembl release 89: ENSG00000160284, ENSG00000274679 - Ensembl, May 2017
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.
5. "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.

Further reading

• 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. 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.