Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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5091 to 5100 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

5091
GDP dissociation inhibitor 1
1A, GDIL, MRX41, MRX48, OPHN2, RABGD1A, RABGDIA, XAP-4, XLID41
Amyotrophic lateral sclerosis, Intellectual developmental disorder, x-linked, Intellectual developmental disorder, Motor neuron disease, X-linked intellectual disability

5092
GDP dissociation inhibitor 2
HEL-S-46e, RABGDIB
Breast cancer, Esophageal squamous cell carcinoma, Prostate cancer, Systemic lupus erythematosus, Diabetes mellitus type 1, Diabetes mellitus type 2

5093
Glial cell derived neurotrophic factor
ATF, ATF1, ATF2, HFB1-GDNF, HSCR3
Amphetamine or sympathomimetic abuse, Anorexia nervosa, Anxiety disorder, Bipolar disorder, Haddad syndrome, Congenital central hypoventilation syndrome, Degenerative disorder, Diverticular disease, Dyskinesia, drug-induced, Epilepsy, Glioblastoma, Glioma, Glomerulonephritis, Hirschsprung disease, Huntington disease
View all (13 more)

5094
Glycerophosphodiester phosphodiesterase domain containing 1
GDE4
Ocular hypertension, Retinitis pigmentosa

5095
Glycerophosphodiester phosphodiesterase domain containing 3
GDE7
Lipidoses, Lipoidosis

5096
Glycerophosphodiester phosphodiesterase domain containing 5
GDE2, PP1665
Colorectal cancer, Corneal dystrophy, Coronary artery disease, Endometrial neoplasms, Eye disease

5097
GTP binding protein overexpressed in skeletal muscle
KIR
Coronary artery disease, Metabolic syndrome, Diabetes mellitus type 2

5098
Gem nuclear organelle associated protein 2
SIP1, SIP1-delta
Spinal muscular atrophy

5099
Gem nuclear organelle associated protein 4
HC56, HCAP1, HHRF-1, NEDMCR, p97
Congenital cataract, Global developmental delay, Neurodevelopmental disorder

5100
Gem nuclear organelle associated protein 5
GEMIN-5, NEDCAM
Nonsyndromic intellectual disability, Essential tremor, Neurodevelopmental disorder, Venous thromboembolism