Oculocutaneous albinism type II Gene Set

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

49 genes co-occuring with the disease Oculocutaneous albinism type II in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Symbol Name Standardized Value
OCA2 oculocutaneous albinism II 3.352
TYR tyrosinase 2.419
SLC24A5 solute carrier family 24 (sodium/potassium/calcium exchanger), member 5 2.256
SLC45A2 solute carrier family 45, member 2 2.179
HPS4 Hermansky-Pudlak syndrome 4 2.002
SLC38A8 solute carrier family 38, member 8 1.947
TYRP1 tyrosinase-related protein 1 1.944
SLC24A4 solute carrier family 24 (sodium/potassium/calcium exchanger), member 4 1.93
HPS6 Hermansky-Pudlak syndrome 6 1.916
HPS3 Hermansky-Pudlak syndrome 3 1.853
ASIP agouti signaling protein 1.842
GABRA5 gamma-aminobutyric acid (GABA) A receptor, alpha 5 1.825
HPS5 Hermansky-Pudlak syndrome 5 1.817
HERC2 HECT and RLD domain containing E3 ubiquitin protein ligase 2 1.788
LRMDA leucine rich melanocyte differentiation associated 1.77
LUZP2 leucine zipper protein 2 1.68
RCC1L RCC1 like 1.65
GABRG3 gamma-aminobutyric acid (GABA) A receptor, gamma 3 1.631
MC1R melanocortin 1 receptor (alpha melanocyte stimulating hormone receptor) 1.624
TUBGCP5 tubulin, gamma complex associated protein 5 1.538
BLOC1S3 biogenesis of lysosomal organelles complex-1, subunit 3 1.501
OTUD7A OTU deubiquitinase 7A 1.473
RBSN rabenosyn, RAB effector 1.38
GPR143 G protein-coupled receptor 143 1.336
UBE3A ubiquitin protein ligase E3A 1.296
NIPA2 non imprinted in Prader-Willi/Angelman syndrome 2 1.275
TRPM1 transient receptor potential cation channel, subfamily M, member 1 1.264
LRRC49 leucine rich repeat containing 49 1.26
SNRPN small nuclear ribonucleoprotein polypeptide N 1.259
POM121L12 POM121 transmembrane nucleoporin-like 12 1.253
LCT lactase 1.23
FRMD7 FERM domain containing 7 1.228
AP3D1 adaptor-related protein complex 3, delta 1 subunit 1.224
FYCO1 FYVE and coiled-coil domain containing 1 1.215
GABRB3 gamma-aminobutyric acid (GABA) A receptor, beta 3 1.21
KLF13 Kruppel-like factor 13 1.209
ANKRD24 ankyrin repeat domain 24 1.204
BLOC1S6 biogenesis of lysosomal organelles complex-1, subunit 6, pallidin 1.197
NHS Nance-Horan syndrome (congenital cataracts and dental anomalies) 1.193
PAX6 paired box 6 1.179
DTNBP1 dystrobrevin binding protein 1 1.166
DCT dopachrome tautomerase 1.137
UNC50 unc-50 homolog (C. elegans) 1.106
ETFA electron-transfer-flavoprotein, alpha polypeptide 1.092
UXS1 UDP-glucuronate decarboxylase 1 1.06
GLO1 glyoxalase I 1.059
BLOC1S5 biogenesis of lysosomal organelles complex-1, subunit 5, muted 1.043
SLC4A11 solute carrier family 4, sodium borate transporter, member 11 1.043
DOK6 docking protein 6 1.018