SFRS17A

SFRS17A
Identifikatori
Aliasi	AKAP17A
Vanjski ID-jevi	OMIM: 312095, 465000 HomoloGene: 3728 GeneCards: AKAP17A
Obrazac RNK ekspresije
	; ;
	Više referentnih podataka o ekspresiji
Ontologija gena
Molekularna funkcija	• GO:0001948, GO:0016582 vezivanje za proteine; • nucleic acid binding; • vezivanje sa RNK; • protein kinase A binding;
Ćelijska komponenta	• nuclear speck; • spliceosomal complex; • jedro; • citosol;
Biološki proces	• B cell activation; • mRNA processing; • GO:0009373 regulation of transcription, DNA-templated; • Prerada RNK; • GO:0072468 Transdukcija signala; • regulation of RNA splicing;
	Izvori:Amigo / QuickGO
Ortolozi
	8227
	n/a
	n/a
	n/a
	Q02040
	n/a
	NM_005088
	n/a
	NP_005079
	n/a
	Wikipodaci
Pogledaj/uredi – čovjek

Arginin-serin-bogati faktor prerade 17A je protein koji je kod ljudi kodiran genom SFRS17A.^[2]^[3]^[4]

Reference

↑ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
↑ Ried K, Rao E, Schiebel K, Rappold GA (Dec 1998). "Gene duplications as a recurrent theme in the evolution of the human pseudoautosomal region 1: isolation of the gene ASMTL". Hum Mol Genet. 7 (11): 1771–8. doi:10.1093/hmg/7.11.1771. PMID 9736779.
↑ Voland JR, Wyzykowski RJ, Huang M, Dutton RW (Dec 1992). "Cloning and sequencing of a trophoblast-endothelial-activated lymphocyte surface protein: cDNA sequence and genomic structure". Proc Natl Acad Sci U S A. 89 (21): 10425–9. doi:10.1073/pnas.89.21.10425. PMC 50351. PMID 1438229.
↑ "Entrez Gene: CXYorf3 chromosome X and Y open reading frame 3".

Dopunska literatura

Ellison JW, Ramos C, Yen PH, Shapiro LJ (1993). "Structure and expression of the human pseudoautosomal gene XE7". Hum. Mol. Genet. 1 (9): 691–6. PMID 1302606.
Bonaldo MF, Lennon G, Soares MB (1997). "Normalization and subtraction: two approaches to facilitate gene discovery". Genome Res. 6 (9): 791–806. doi:10.1101/gr.6.9.791. PMID 8889548.
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.
Hillman RT, Green RE, Brenner SE (2005). "An unappreciated role for RNA surveillance". Genome Biol. 5 (2): R8. doi:10.1186/gb-2004-5-2-r8. PMC 395752. PMID 14759258.
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.
Rual JF, Venkatesan K, Hao T, et al. (2005). "Towards a proteome-scale map of the human protein-protein interaction network". Nature. 437 (7062): 1173–8. doi:10.1038/nature04209. PMID 16189514.
Mangs AH, Speirs HJ, Goy C, et al. (2006). "XE7: a novel splicing factor that interacts with ASF/SF2 and ZNF265". Nucleic Acids Res. 34 (17): 4976–86. doi:10.1093/nar/gkl660. PMC 1635291. PMID 16982639.
Olsen JV, Blagoev B, Gnad F, et al. (2006). "Global, in vivo, and site-specific phosphorylation dynamics in signaling networks". Cell. 127 (3): 635–48. doi:10.1016/j.cell.2006.09.026. PMID 17081983.
Ewing RM, Chu P, Elisma F, et al. (2007). "Large-scale mapping of human protein-protein interactions by mass spectrometry". Mol. Syst. Biol. 3 (1): 89. doi:10.1038/msb4100134. PMC 1847948. PMID 17353931.

[1] "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.

[pmid9736779-2] Ried K, Rao E, Schiebel K, Rappold GA (Dec 1998). "Gene duplications as a recurrent theme in the evolution of the human pseudoautosomal region 1: isolation of the gene ASMTL". Hum Mol Genet. 7 (11): 1771–8. doi:10.1093/hmg/7.11.1771. PMID 9736779.

[pmid1438229-3] Voland JR, Wyzykowski RJ, Huang M, Dutton RW (Dec 1992). "Cloning and sequencing of a trophoblast-endothelial-activated lymphocyte surface protein: cDNA sequence and genomic structure". Proc Natl Acad Sci U S A. 89 (21): 10425–9. doi:10.1073/pnas.89.21.10425. PMC 50351. PMID 1438229.

[entrez-4] "Entrez Gene: CXYorf3 chromosome X and Y open reading frame 3".

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