PRPF40B

PRPF40B
Identifiers
Aliases	PRPF40B, HYPC, pre-mRNA processing factor 40 homolog B
External IDs	MGI: 1925583 HomoloGene: 81828 GeneCards: PRPF40B
Gene location (Human)
Chr.	Chromosome 12 (human)[1]
End	49,644,666 bp[1]
Gene location (Mouse)
Chr.	Chromosome 15 (mouse)[2]
End	99,317,018 bp[2]
Gene ontology
Molecular function	• RNA binding;
Cellular component	• U1 snRNP; • nuclear speck; • U2-type prespliceosome; • cell nucleus;
Biological process	• mRNA splicing, via spliceosome; • mRNA processing; • RNA splicing; • mRNA cis splicing, via spliceosome;
	Sources:Amigo / QuickGO
Orthologs
	25766
	54614
	ENSG00000110844
	ENSMUSG00000023007
	Q6NWY9
	Q80W14
NM_001031698; NM_012272; NM_001363607; NM_001379030; NM_001379031;
	NM_001379032; NM_001379033; NM_001379034; NM_001379035; NM_001379036; NM_001379037
	NM_018786; NM_001348256
NP_001026868; NP_036404; NP_001350536; NP_001365959; NP_001365960;
	NP_001365961; NP_001365962; NP_001365963; NP_001365964; NP_001365965; NP_001365966
NP_061256; NP_001335185; NP_001357561; NP_001357562; NP_001357563;
	NP_001357564
	Wikidata
View/Edit Human	View/Edit Mouse

Pre-mRNA-processing factor 40 homolog B is a protein that in humans that is encoded by the PRPF40B gene. [5]

References

Buschdorf JP, Strätling WH (Feb 2004). "A WW domain binding region in methyl-CpG-binding protein MeCP2: impact on Rett syndrome". Journal of Molecular Medicine. 82 (2): 135–43. doi:10.1007/s00109-003-0497-9. PMID 14618241. S2CID 9685491.
Faber PW, Barnes GT, Srinidhi J, Chen J, Gusella JF, MacDonald ME (Sep 1998). "Huntingtin interacts with a family of WW domain proteins". Human Molecular Genetics. 7 (9): 1463–74. doi:10.1093/hmg/7.9.1463. PMID 9700202.

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