Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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5171 to 5180 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

5171
Gap junction protein beta 4
CX30.3, EKV, EKVP2
Deafness, Erythrokeratodermia variabilis, Greither disease

5172
Gap junction protein beta 5
CX31.1
Skin neoplasms

5173
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
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5174
Gap junction protein beta 7
CX25, bA136M9.1, connexin25
Atrial fibrillation

5175
Gap junction protein gamma 1
CX45, GJA7
Hypertension, Oligodendroglioma

5176
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

5177
Gap junction protein delta 2
CX36, GJA9
Atrial fibrillation, Congenital left-sided heart lesions, Eye disease, Hyperopia, Myopia, Open angle glaucoma

5178
Gap junction protein delta 4
CX40.1
Alzheimer disease

5179
Gap junction protein epsilon 1
CX23
Non-neoplastic peripheral nervous system disease, Peripheral nervous system disease, Peripheral neuropathy

5180
Glycerol kinase
GK1, GKD
Glycerol kinase deficiency, Myocardial ischemia