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71492 Bbs7

71492

Bbs7

Bardet-Biedl syndrome 7 (human)

protein-coding

Mus musculus

基因描述

Type Description
Definition Bardet-Biedl syndrome 7 (human)

研究结论

Date Results Publications
2013-11-16 12:00:00 BBS7 is not required for the localization of ciliary membrane proteins polycystin-1, polycystin-2, or bitter taste receptors, but absence of BBS7 leads to abnormal accumulation of the dopamine D1 receptor to the ciliary membrane 23572516
2012-09-08 10:30:00 Knockout of Bbs7 combined with a hypomorphic Ift88 allele (orpk as a model for Shh dysfuction) results in embryonic lethality with e12.5 embryos having exencephaly, pericardial edema, cleft palate and abnormal limb development. 22228099

名称对应

Type IDs
Synonymous 8430406N16Rik
Gene
UniProtKB-ID: BBS7_MOUSE
UniprotKB: Q8K2G4
UniParc: UPI00000E8E26, UPI00000286A6, UPI0000022CA0
EMBL: AK050291, AF521645, AK018389, BC031505
Ensembl: ENSMUSG00000037325
KO: mmu:71492
Nucleutide sequences
EMBL-CDS: AAO16027.1, BAC34169.1, AAH31505.1, BAB31190.1
Ensembl_TRS: ENSMUST00000040148, ENSMUST00000108156
Protein sequencees
Ensembl_PRO: ENSMUSP00000047273, ENSMUSP00000103791
RefSeq: XP_036019223.1, XP_006535599.1, NP_082086.2, XP_006535598.1
Others
UniRef100: UniRef100_Q8K2G4
UniRef90: UniRef90_Q8K2G4
UniRef50: UniRef50_Q8K2G4
UniGene: Mm.286187
CCDS: CCDS17314.2

全选

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