Type | Description |
---|---|
Definition | crumbs family member 1, photoreceptor morphogenesis associated |
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 |
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
|
{{proteinIndex+1}} | mRNA | Protein | UniprotKB | Description | ||||
---|---|---|---|---|---|---|---|---|
Refseq |
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