Type | Description |
---|---|
Definition | Bardet-Biedl syndrome 7 (human) |
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 |
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
|
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Refseq |
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