Oculocutaneous albinism type IB Gene Set

Dataset DISEASES Text-mining Gene-Disease Association Evidence Scores 2025
Category disease or phenotype associations
Type disease
Similar Terms
Downloads & Tools

Genes

28 genes co-occuring with the disease Oculocutaneous albinism type IB 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 2.531
TYR tyrosinase 2.414
SLC45A2 solute carrier family 45, member 2 2.225
HPD 4-hydroxyphenylpyruvate dioxygenase 2.193
GPR143 G protein-coupled receptor 143 1.994
TYRP1 tyrosinase-related protein 1 1.883
SLC24A5 solute carrier family 24 (sodium/potassium/calcium exchanger), member 5 1.577
FAH fumarylacetoacetate hydrolase (fumarylacetoacetase) 1.534
LRMDA leucine rich melanocyte differentiation associated 1.406
SLITRK6 SLIT and NTRK-like family, member 6 1.32
BLOC1S3 biogenesis of lysosomal organelles complex-1, subunit 3 1.312
SLC16A12 solute carrier family 16, member 12 1.308
HPS6 Hermansky-Pudlak syndrome 6 1.304
MYO5A myosin VA (heavy chain 12, myoxin) 1.288
FRMD7 FERM domain containing 7 1.287
BLOC1S6 biogenesis of lysosomal organelles complex-1, subunit 6, pallidin 1.256
PLCG2 phospholipase C, gamma 2 (phosphatidylinositol-specific) 1.253
HPS3 Hermansky-Pudlak syndrome 3 1.242
KLLN killin, p53-regulated DNA replication inhibitor 1.201
ZNF469 zinc finger protein 469 1.191
DCT dopachrome tautomerase 1.167
SLITRK1 SLIT and NTRK-like family, member 1 1.154
GNAT2 guanine nucleotide binding protein (G protein), alpha transducing activity polypeptide 2 1.138
PRUNE2 prune homolog 2 (Drosophila) 1.125
MC1R melanocortin 1 receptor (alpha melanocyte stimulating hormone receptor) 1.043
CNGB3 cyclic nucleotide gated channel beta 3 1.039
CNGA3 cyclic nucleotide gated channel alpha 3 1.031
COL8A2 collagen, type VIII, alpha 2 1.023