MBNL3

MBNL3
Identifikatori
Aliasi	MBNL3
Vanjski ID-jevi	OMIM: 300413 MGI: 2444912 HomoloGene: 23101 GeneCards: MBNL3
Lokacija gena (čovjek) Hrom. Hromosom X Bend Xq26.2 Početak 132,369,317 bp Kraj 132,489,968 bp
Lokacija gena (miš) Hrom. Hromosom X (miš) Bend X|X A5 Početak 50,206,146 bp Kraj 50,295,409 bp
Obrazac RNK ekspresije Više referentnih podataka o ekspresiji
Ontologija gena Molekularna funkcija • GO:0001948, GO:0016582 vezivanje za proteine • vezivanje iona metala • vezivanje sa RNK • GO:0001200, GO:0001133, GO:0001201 DNA-binding transcription factor activity, RNA polymerase II-specific Ćelijska komponenta • citoplazma • jedro • nukleoplazma Biološki proces • multicellular organism development • regulation of RNA splicing • mRNA processing • negative regulation of myoblast differentiation • Prerada RNK • regulation of alternative mRNA splicing, via spliceosome • GO:0044324, GO:0003256, GO:1901213, GO:0046019, GO:0046020, GO:1900094, GO:0061216, GO:0060994, GO:1902064, GO:0003258, GO:0072212 regulation of transcription by RNA polymerase II Izvori:Amigo / QuickGO
Ortolozi
Vrste	Čovjek	Miš
Entrez	55796	171170
Ensembl	ENSG00000076770	ENSMUSG00000036109
UniProt	Q9NUK0	Q8R003
RefSeq (mRNK)	NM_001170701 NM_001170702 NM_001170703 NM_001170704 NM_018388 NM_133486	NM_134163 NM_001310515
RefSeq (bjelančevina)	NP_001164172 NP_001164173 NP_001164174 NP_001164175 NP_060858 NP_597846	NP_001297444 NP_598924
Lokacija (UCSC)	Chr X: 132.37 – 132.49 Mb	Chr X: 50.21 – 50.3 Mb
PubMed pretraga
Wikipodaci
Pogledaj/uredi – čovjek Pogledaj/uredi – miš

Sljepomišićnoliki regulacijski protein 3 je protein koji je kod ljudi kodiran genom MBNL3.

Dopunska literatura

• Fardaei M, Rogers MT, Thorpe HM, et al. (2002). "Three proteins, MBNL, MBLL and MBXL, co-localize in vivo with nuclear foci of expanded-repeat transcripts in DM1 and DM2 cells". Hum. Mol. Genet. 11 (7): 805–14. doi:10.1093/hmg/11.7.805. PMID 11929853.
• 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.
• Ho TH, Charlet-B N, Poulos MG, et al. (2005). "Muscleblind proteins regulate alternative splicing". EMBO J. 23 (15): 3103–12. doi:10.1038/sj.emboj.7600300. PMC 514918. PMID 15257297.
• 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.
• Ross MT, Grafham DV, Coffey AJ, et al. (2005). "The DNA sequence of the human X chromosome". Nature. 434 (7031): 325–37. doi:10.1038/nature03440. PMC 2665286. PMID 15772651.
• Self JE, Ennis S, Collins A, et al. (2006). "Fine mapping of the X-linked recessive congenital idiopathic nystagmus locus at Xq24-q26.3". Mol. Vis. 12: 1211–6. PMID 17102799.