Genesⓘ

Dataset:
? Reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "G"
181 to 190 of 533 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

181
Gap junction protein beta 1
CMTX, CMTX1, CX32
Hepatocellular carcinoma, Renal cell carcinoma, Cerebellar ataxia, Charcot-marie-tooth disease, Charcot-marie-tooth disease, x-linked, Dejerine-sottas disease, Gout, Hypertrophic neuropathy, Liver neoplasm, Lung neoplasms, Peripheral neuropathy, Peroneal muscle atrophy, Prostate cancer, Roussy-levy syndrome, Sensory neuropathy
View all (3 more)

182
Gap junction protein beta 2
BAPS, CX26, DFNA3, DFNA3A, DFNB1, DFNB1A, HID, KID, NSRD1, PPK
Autism, Isolated sensorineural deafness, Keratitis ichthyosis hearing loss syndrome, Nonsyndromic hearing loss, Bart-pumphrey syndrome, Deafness, Deafness, digenic, Deafness, x-linked, Hearing impairment, Hearing loss, Ichthyosis, Keratitis, Keratitis-ichthyosis-deafness syndrome, Noonan syndrome, Porokeratosis
View all (7 more)

183
Gap junction protein beta 3
CX31, DFNA2, DFNA2B, EKV, EKVP1
Isolated sensorineural deafness, Nonsyndromic hearing loss, Deafness, Autosomal dominant sensorineural deafness, Deafness, digenic, Dermatologic disorder, Erythrokeratodermia variabilis, Greither disease, Hearing impairment, Hearing loss, Neuropathy, ataxia, and retinitis pigmentosa, Non-neoplastic peripheral nervous system disease, Peripheral nervous system disease, Peripheral neuropathy, Peripheral neuropathy with sensorineural hearing impairment syndrome
View all (1 more)

184
Gap junction protein beta 5
CX31.1
Skin neoplasm

185
Glycerol kinase
GK1, GKD
Glycerol kinase deficiency, Liver cirrhosis, Myocardial ischemia

186
Galactosidase alpha
GALA
Angiokeratoma, Cardiomyopathy, Fabry disease, Hypertrophic cardiomyopathy, Intellectual developmental disorder, x-linked, Nephrotic syndrome

187
Glypican 3
DGSX, GTR2-2, MXR7, OCI-5, SDYS, SGB, SGBS, SGBS1
Hepatocellular carcinoma, Desbuquois syndrome, Global developmental delay, Insomnia, Intellectual developmental disorder, Mesothelioma, Simpson-golabi-behmel syndrome, Wilms tumor

188
Galactosidase beta 1
EBP, ELNR1, MPS4B
Asthma, Eczema, Bone disease, Celiac disease, Obstructive pulmonary disease, Congenital cartilage disorder, Contact dermatitis, Atopic dermatitis, Desbuquois syndrome, Gm1 gangliosidosis, Hepatocellular carcinoma, Mucopolysaccharidosis, Multiple sclerosis, Osteochondrodysplasias, Progressive intrahepatic cholestasis
View all (6 more)

189
G protein-coupled receptor 78
-
Bipolar disorder, Diffuse gastric adenocarcinoma, Gastric cancer, Neuroblastoma, Schizophrenia, Systemic lupus erythematosus

190
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