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Gene–disease association summaries
Gene–Disease Browser
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| Gene |
Disease |
Score |
Actions |
|
OTUD4
(HGNC:24949)
|
prostate cancer
(MONDO_0008315)
|
Limited
|
|
|
GSX2
(HGNC:24959)
|
diencephalic-mesencephalic junction dysplasia
(MONDO_0017868)
|
Limited
|
|
|
ZC4H2
(HGNC:24931)
|
Wieacker-Wolff syndrome
(MONDO_0010758)
|
Strong
|
|
|
STBD1
(HGNC:24854)
|
Parkinson disease
(MONDO_0005180)
|
Limited
|
|
|
LARP7
(HGNC:24912)
|
microcephalic primordial dwarfism, Alazami type
(MONDO_0014031)
|
Strong
|
|
|
OTUD4
(HGNC:24949)
|
breast cancer
(MONDO_0007254)
|
Limited
|
|
|
CCDC47
(HGNC:24856)
|
trichohepatoneurodevelopmental syndrome
(MONDO_0032645)
|
Strong
|
|
|
PNPLA4
(HGNC:24887)
|
epilepsy
(MONDO_0005027)
|
Limited
|
|
|
YIPF5
(HGNC:24877)
|
neonatal diabetes mellitus
(MONDO_0016391)
|
Strong
|
|
|
MOGS
(HGNC:24862)
|
congenital disorder of glycosylation
(MONDO_0015286)
|
Strong
|
|
|
CCDC91
(HGNC:24855)
|
breast cancer
(MONDO_0007254)
|
Limited
|
|
|
CEP104
(HGNC:24866)
|
Joubert syndrome
(MONDO_0018772)
|
Moderate
|
|
|
ENHO
(HGNC:24838)
|
type 2 diabetes mellitus
(MONDO_0005148)
|
Limited
|
|
|
FN3K
(HGNC:24822)
|
diabetes mellitus
(MONDO_0005015)
|
Limited
|
|
|
CIBAR2
(HGNC:24781)
|
ulcerative colitis
(MONDO_0005101)
|
Disputed
|
|
|
VWA2
(HGNC:24709)
|
congenital anomaly of kidney and urinary tract
(MONDO_0019719)
|
Limited
|
|
|
GPRASP1
(HGNC:24834)
|
arteriovenous hemangioma/malformation
(MONDO_0001256)
|
Limited
|
|
|
LONRF2
(HGNC:24788)
|
colorectal cancer
(MONDO_0005575)
|
Limited
|
|
|
KLRG2
(HGNC:24778)
|
prostate cancer
(MONDO_0008315)
|
Limited
|
|
|
PTCD3
(HGNC:24717)
|
Leigh syndrome
(MONDO_0009723)
|
Strong
|
|