Oculocutaneous albinism type IA Gene Set
Genes
28 genes co-occuring with the disease Oculocutaneous albinism type IA in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
| Symbol |
Name |
Standardized Value |
|
TYR
|
tyrosinase
|
2.544
|
|
OCA2
|
oculocutaneous albinism II
|
2.378
|
|
FES
|
FES proto-oncogene, tyrosine kinase
|
1.683
|
|
SLC45A2
|
solute carrier family 45, member 2
|
1.664
|
|
TYRP1
|
tyrosinase-related protein 1
|
1.663
|
|
INPP5F
|
inositol polyphosphate-5-phosphatase F
|
1.591
|
|
EDEM1
|
ER degradation enhancer, mannosidase alpha-like 1
|
1.576
|
|
CYP20A1
|
cytochrome P450, family 20, subfamily A, polypeptide 1
|
1.548
|
|
PMEL
|
premelanosome protein
|
1.357
|
|
DCT
|
dopachrome tautomerase
|
1.344
|
|
LRBA
|
LPS-responsive vesicle trafficking, beach and anchor containing
|
1.328
|
|
ABCA4
|
ATP-binding cassette, sub-family A (ABC1), member 4
|
1.297
|
|
LIPC
|
lipase, hepatic
|
1.259
|
|
VPS33A
|
vacuolar protein sorting 33 homolog A (S. cerevisiae)
|
1.24
|
|
CANX
|
calnexin
|
1.229
|
|
MC1R
|
melanocortin 1 receptor (alpha melanocyte stimulating hormone receptor)
|
1.221
|
|
FKBP14
|
FK506 binding protein 14, 22 kDa
|
1.194
|
|
SBF1
|
SET binding factor 1
|
1.179
|
|
ZNF469
|
zinc finger protein 469
|
1.121
|
|
RPL38
|
ribosomal protein L38
|
1.11
|
|
HBB
|
hemoglobin, beta
|
1.104
|
|
STX16
|
syntaxin 16
|
1.095
|
|
BCKDHB
|
branched chain keto acid dehydrogenase E1, beta polypeptide
|
1.082
|
|
RAB38
|
RAB38, member RAS oncogene family
|
1.075
|
|
PRUNE2
|
prune homolog 2 (Drosophila)
|
1.055
|
|
MNT
|
MAX network transcriptional repressor
|
1.029
|
|
RPS27
|
ribosomal protein S27
|
1.025
|
|
MTO1
|
mitochondrial tRNA translation optimization 1
|
1.007
|
