coats disease Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_7765)
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24 genes co-occuring with the disease coats disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
NDP Norrie disease (pseudoglioma) 1.95535
CTC1 CTS telomere maintenance complex component 1 1.68362
TSPAN12 tetraspanin 12 1.41665
AGGF1 angiogenic factor with G patch and FHA domains 1 1.28654
CRB1 crumbs family member 1, photoreceptor morphogenesis associated 1.28435
IKBKG inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase gamma 1.26081
GLMN glomulin, FKBP associated protein 1.23343
FZD4 frizzled class receptor 4 1.14985
PDCD10 programmed cell death 10 1.09797
VEGFA vascular endothelial growth factor A 0.950769
KRIT1 KRIT1, ankyrin repeat containing 0.935799
SOX18 SRY (sex determining region Y)-box 18 0.924213
TINF2 TERF1 (TRF1)-interacting nuclear factor 2 0.878605
GCNT2 glucosaminyl (N-acetyl) transferase 2, I-branching enzyme (I blood group) 0.825358
LRP5 low density lipoprotein receptor-related protein 5 0.753713
FOXC2 forkhead box C2 0.741517
RASA1 RAS p21 protein activator (GTPase activating protein) 1 0.656046
ACVRL1 activin A receptor type II-like 1 0.595623
PAX6 paired box 6 0.391513
NOTCH3 notch 3 0.333218
NOTCH4 notch 4 0.305226
FN1 fibronectin 1 0.237357
MYCN v-myc avian myelocytomatosis viral oncogene neuroblastoma derived homolog 0.22937
TERT telomerase reverse transcriptase 0.217352