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Gene–disease association summaries
Gene–Disease Browser
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| Gene |
Disease |
Score |
Actions |
|
TRMT5
(HGNC:23141)
|
combined oxidative phosphorylation defect type 26
(MONDO_0014684)
|
Limited
|
|
|
RNF150
(HGNC:23138)
|
chronic obstructive pulmonary disease
(MONDO_0005002)
|
Limited
|
|
|
SLC29A4
(HGNC:23097)
|
type 2 diabetes mellitus
(MONDO_0005148)
|
Limited
|
|
|
ARHGAP33
(HGNC:23085)
|
intellectual disability
(MONDO_0001071)
|
Limited
|
|
|
TRAPPC2
(HGNC:23068)
|
spondyloepiphyseal dysplasia tarda, X-linked
(MONDO_0010737)
|
Definitive
|
|
|
TRAPPC6B
(HGNC:23066)
|
intellectual disability
(MONDO_0001071)
|
Moderate
|
|
|
ALG3
(HGNC:23056)
|
congenital disorder of glycosylation
(MONDO_0015286)
|
Strong
|
|
|
BRK1
(HGNC:23057)
|
von Hippel-Lindau disease
(MONDO_0008667)
|
Disputed
|
|
|
ALG3
(HGNC:23056)
|
ALG3-congenital disorder of glycosylation
(MONDO_0010998)
|
Strong
|
|
|
TM7SF3
(HGNC:23049)
|
Kallmann syndrome
(MONDO_0018800)
|
Limited
|
|
|
TM7SF3
(HGNC:23049)
|
intellectual disability
(MONDO_0001071)
|
Limited
|
|
|
ARMC2
(HGNC:23045)
|
male infertility
(MONDO_0005372)
|
Strong
|
|
|
CPB1
(HGNC:2299)
|
pancreatic ductal adenocarcinoma
(MONDO_0005184)
|
Limited
|
|
|
TMC4
(HGNC:22998)
|
metabolic dysfunction-associated steatotic liver disease
(MONDO_0013209)
|
Disputed
|
|
|
PEX26
(HGNC:22965)
|
peroxisome biogenesis disorder
(MONDO_0019234)
|
Strong
|
|
|
DEPTOR
(HGNC:22953)
|
lung cancer
(MONDO_0008903)
|
Limited
|
|
|
GPR155
(HGNC:22951)
|
lung cancer
(MONDO_0008903)
|
Limited
|
|
|
SLC25A2
(HGNC:22921)
|
gastric cancer
(MONDO_0001056)
|
Disputed
|
|
|
COX6B1
(HGNC:2280)
|
cytochrome-c oxidase deficiency disease
(MONDO_0009068)
|
Moderate
|
|
|
COX6A2
(HGNC:2279)
|
cytochrome-c oxidase deficiency disease
(MONDO_0009068)
|
Moderate
|
|