Ocular albinism with sensorineural deafness Gene Set

Dataset DISEASES Text-mining Gene-Disease Association Evidence Scores 2025
Category disease or phenotype associations
Type disease
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Genes

33 genes co-occuring with the disease Ocular albinism with sensorineural deafness in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Symbol Name Standardized Value
MITF microphthalmia-associated transcription factor 1.818
TBL1Y transducin (beta)-like 1, Y-linked 1.798
TBL1XR1 transducin (beta)-like 1 X-linked receptor 1 1.489
TYR tyrosinase 1.475
CORO2A coronin, actin binding protein, 2A 1.443
SOX10 SRY (sex determining region Y)-box 10 1.347
PEX26 peroxisomal biogenesis factor 26 1.303
PEX11B peroxisomal biogenesis factor 11 beta 1.295
DSE dermatan sulfate epimerase 1.281
PEX12 peroxisomal biogenesis factor 12 1.253
GJB4 gap junction protein, beta 4, 30.3kDa 1.248
PEX16 peroxisomal biogenesis factor 16 1.214
PEX13 peroxisomal biogenesis factor 13 1.204
PEX10 peroxisomal biogenesis factor 10 1.194
CHST14 carbohydrate (N-acetylgalactosamine 4-0) sulfotransferase 14 1.192
HCCS holocytochrome c synthase 1.18
ZNF469 zinc finger protein 469 1.174
PEX2 peroxisomal biogenesis factor 2 1.159
EDN3 endothelin 3 1.145
ATP6V1B2 ATPase, H+ transporting, lysosomal 56/58kDa, V1 subunit B2 1.143
PEX3 peroxisomal biogenesis factor 3 1.134
TBC1D24 TBC1 domain family, member 24 1.117
PRDM5 PR domain containing 5 1.112
PEX19 peroxisomal biogenesis factor 19 1.112
DDB1 damage-specific DNA binding protein 1, 127kDa 1.099
CAND1 cullin-associated and neddylation-dissociated 1 1.088
GPS2 G protein pathway suppressor 2 1.078
PEX6 peroxisomal biogenesis factor 6 1.04
ERCC8 excision repair cross-complementation group 8 1.028
SLC29A3 solute carrier family 29 (equilibrative nucleoside transporter), member 3 1.027
TBL1X transducin (beta)-like 1X-linked 1.025
EP300 E1A binding protein p300 1.025
ING1 inhibitor of growth family, member 1 1.004