CRYAB, crystallin alpha B, 1410

N. diseases: 200; N. variants: 30
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104894201
rs104894201
Entrez Id: 1410
Gene Symbol: CRYAB
CRYAB
CUI: C0086543
Disease:
Cataract
0.040 GeneticVariation BEFREE To understand the mechanism of VP1-001, we tested the ability of its enantiomer, ent-VP1-001, to bind and stabilize αB-crystallin (cryAB) in vitro and to produce a similar therapeutic effect in cryAB(R120G) mutant and aged wild-type mice with cataracts. 31369034 2019
dbSNP: rs104894201
rs104894201
Entrez Id: 1410
Gene Symbol: CRYAB
CRYAB
CUI: C0086543
Disease:
Cataract
0.040 GeneticVariation BEFREE To investigate the mechanism by which the α-crystallin mutations Cryaa-R49C and Cryab-R120G lead to cataract formation, we determined whether these mutations cause an altered expression of specific transcripts in the lens at an early postnatal age by RNA-seq analysis. 29338044 2018
dbSNP: rs104894201
rs104894201
Entrez Id: 1410
Gene Symbol: CRYAB
CRYAB
CUI: C0086543
Disease:
Cataract
0.040 GeneticVariation BEFREE The most promising compound improved lens transparency in the R49C cryAA and R120G cryAB mouse models of hereditary cataract. 26542570 2015
dbSNP: rs104894201
rs104894201
Entrez Id: 1410
Gene Symbol: CRYAB
CRYAB
CUI: C0086543
Disease:
Cataract
0.040 GeneticVariation BEFREE These data suggest that the cataract and myopathy pathologies in αB-R120G knock-in mice share common mechanisms, including increased insolubility of αB-crystallin and co-aggregation of αB-crystallin with intermediate filament proteins. 21445271 2011