Embryonal Nuclear Cataract (Disorder) Gene Set
Genes
16 genes associated with the disease Embryonal Nuclear Cataract (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
| Symbol |
Name |
|
BFSP1
|
beaded filament structural protein 1, filensin
|
|
C21ORF2
|
chromosome 21 open reading frame 2
|
|
CHMP4B
|
charged multivesicular body protein 4B
|
|
CRYAA
|
crystallin, alpha A
|
|
CRYBA1
|
crystallin, beta A1
|
|
CRYBB1
|
crystallin, beta B1
|
|
CRYBB3
|
crystallin, beta B3
|
|
CRYGC
|
crystallin, gamma C
|
|
CRYGD
|
crystallin, gamma D
|
|
FTL
|
ferritin, light polypeptide
|
|
GJA3
|
gap junction protein, alpha 3, 46kDa
|
|
GJA8
|
gap junction protein, alpha 8, 50kDa
|
|
HSF4
|
heat shock transcription factor 4
|
|
MIP
|
major intrinsic protein of lens fiber
|
|
NHS
|
Nance-Horan syndrome (congenital cataracts and dental anomalies)
|
|
WFS1
|
Wolfram syndrome 1 (wolframin)
|
