Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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Showing genes starting with "G"
251 to 260 of 674 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

251
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, Hereditary hearing loss, Neuropathy, ataxia, and retinitis pigmentosa, Non-neoplastic peripheral nervous system disease, Peripheral nervous system disease, Peripheral neuropathy
View all (2 more)

252
Gap junction protein beta 4
CX30.3, EKV, EKVP2
Deafness, Erythrokeratodermia variabilis, Greither disease

253
Gap junction protein beta 5
CX31.1
Skin neoplasms

254
Gap junction protein beta 6
CX30, DFNA3, DFNA3B, DFNB1B, ECTD2, ED2, EDH, HED, HED2
Astrocytoma, Isolated sensorineural deafness, Nonsyndromic hearing loss, Basal cell carcinoma, Central nervous system cancer, Clouston syndrome, Deafness, Deafness, x-linked, Ectodermal dysplasia, Glioblastoma, Glioma, Hearing impairment, Hearing loss, Hereditary hearing loss, Keratitis-ichthyosis-deafness syndrome
View all (3 more)

255
Gap junction protein beta 7
CX25, bA136M9.1, connexin25
Atrial fibrillation

256
Gap junction protein gamma 1
CX45, GJA7
Hypertension, Oligodendroglioma

257
Gap junction protein gamma 2
CX46.6, Cx47, GJA12, HLD2, LMPH1C, LMPHM3, PMLDAR, SPG44
Spastic paraplegia, Congenital neurologic anomalies, Lymphedema, Hypomyelinating leukodystrophy, Intellectual developmental disorder, Lymphatic malformation, Pelizaeus-merzbacher disease, Spastic ataxia, Hereditary spastic paraplegia

258
Gap junction protein delta 2
CX36, GJA9
Atrial fibrillation, Congenital left-sided heart lesions, Eye disease, Hyperopia, Myopia, Open angle glaucoma

259
Gap junction protein delta 4
CX40.1
Alzheimer disease

260
Gap junction protein epsilon 1
CX23
Non-neoplastic peripheral nervous system disease, Peripheral nervous system disease, Peripheral neuropathy