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170788 Crb1

170788

Crb1

crumbs family member 1, photoreceptor morphogenesis associated

protein-coding

Mus musculus

基因描述

Type Description
Definition crumbs family member 1, photoreceptor morphogenesis associated

研究结论

Date Results Publications
2021-02-06 13:49:00 CRB1(rd8) mutation influences the age-related macular degeneration phenotype of NRF2 knockout mice and favors choroidal neovascularization. 31918066
2020-09-05 13:55:00 Cytoglobin deficiency potentiates Crb1-mediated retinal degeneration in rd8 mice. 31634437
2020-08-12 12:10:00 CRB1 expression during retinal vascular development. 31718797
2020-05-09 12:14:00 These results suggest that human leber congenital amaurosis 8 can be modeled in the mouse by simultaneously ablating Crb1/2 from the beginning of eye development. 31145883
2019-05-11 12:15:00 The rnv3 model and the models of six novel disruptions of Crb1 are all reliable, novel mouse models for the study of both early and late events associated with posterior segment vascularization. 30372741

名称对应

Type IDs
Synonymous 7530426H14Rik, A930008G09Rik
Gene
UniProtKB-ID: CRUM1_MOUSE
UniprotKB: Q8VHS2
UniParc: UPI00000228A8, UPI00000EB9C6, UPI00001ED77B, UPI000217CB17
EMBL: AK044345, AF406641, AY450552, AL606536, AC138741, AF492496, AC116810, AK044704, CH466520
Ensembl: ENSMUSG00000063681
KO: mmu:170788
Nucleutide sequences
EMBL-CDS: AAL65131.1, AAQ06606.1, BAC32041.1, EDL39531.1, AAR20495.1, BAC31879.1
Ensembl_TRS: ENSMUST00000059825, ENSMUST00000196402
Protein sequencees
Ensembl_PRO: ENSMUSP00000060769, ENSMUSP00000142702
RefSeq: XP_036018373.1, XP_036018381.1, XP_036018367.1, XP_006529280.1, XP_036018377.1, XP_017174558.1, XP_036018359.1, XP_036018351.1, XP_036018357.1, NP_573502.2, XP_036018353.1, XP_030107737.1, XP_036018386.1, XP_036018380.1, XP_030107739.1, XP_036018354.1, XP_006529287.1
Others
UniRef100: UniRef100_Q8VHS2
UniRef90: UniRef90_Q8VHS2
UniRef50: UniRef50_P82279
UniGene: Mm.95700
CCDS: CCDS15336.1

全选

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