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Browse result for Cataract

※ introduction

    A lens disease characterized by clouding of the lens inside the eye which leads to a decrease in vision.

Reference
DiseaseOntology: Cataract


PTMD IDUniProt AccessionEntrez IDGene NameProtein NameOrganism
PTMD00189P086707431
VIM
Vimentin
Homo sapiens
PTMD00571P293171969
EPHA2
Ephrin type-A receptor 2
Homo sapiens
PTMD00712Q53H1255750
AGK
Acylglycerol kinase, mitochondrial
Homo sapiens
PTMD01968A0A140G94510272
CRYAA
Alpha-crystallin A chain [Cleaved into: Alpha-crystallin A; Alpha-crystallin A; Alpha-crystallin A]
Homo sapiens
PTMD01461P025111410
CRYAB
Alpha-crystallin B chain -crystallin)
Homo sapiens
PTMD01054P0248910272
CRYAA
Alpha-crystallin A chain [Cleaved into: Alpha-crystallin A; Alpha-crystallin A; Alpha-crystallin A]
Homo sapiens
PTMD05553P536741414
CRYBB1
Beta-crystallin B1
Homo sapiens
PTMD10204Q8NHU623424
TDRD7
Tudor domain-containing protein 7
Homo sapiens
PTMD11992Q9BQS879443
FYCO1
FYVE and coiled-coil domain-containing protein 1
Homo sapiens
PTMD12765Q9H44412886
CHMP4B
Charged multivesicular body protein 4b
Homo sapiens