5191
|
|
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Gap junction protein alpha 5 |
ATFB11, CX40 |
Atrial fibrillation, Atrial flutter, Atrial standstill, Cardioembolic stroke, Chromosome 1q21.1 deletion syndrome, Congenital heart disease, Gout, Heart disease, Hereditary atrial fibrillation, Hypertension, Hypertrophic cardiomyopathy, Interstitial lung disease, Parkinson disease, Scoliosis, Tetralogy of fallot, Wolff-parkinson-white syndromeView all (1 more) |
5192
|
|
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Gap junction protein alpha 8 |
CAE, CAE1, CTRCT1, CX50, CZP1, MP70 |
Anterior segment mesenchymal dysgenesis, Atrial fibrillation, Atrial flutter, Cardioembolic stroke, Cataract, Cataract-microcornea syndrome, Congenital cataract, Chromosome 1q21.1 deletion syndrome, Congenital sclerocornea, Congenital total cataract, Nuclear cataract, Sutural cataract, Gout, Microphthalmos, Schizophrenia, ScoliosisView all (1 more) |
5193
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|
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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, Congenital pes cavus, Dejerine-sottas disease, Gout, Hereditary motor and sensory neuropathies, Hypertrophic neuropathy, Liver neoplasms, Lung neoplasms, Peripheral neuropathy, Peroneal muscle atrophy, Prostate cancer, Roussy-levy syndrome, Sensory neuropathy, Spinocerebellar ataxia, x-linked, Diabetes mellitus type 2, X-linked progressive cerebellar ataxiaView all (5 more) |
5194
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|
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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, Conductive hearing loss, Congenital ear anomaly, Deafness, Deafness, digenic, Deafness, x-linked, Hearing impairment, Hearing loss, Hereditary hearing loss, Ichthyosis, Keratitis, Keratitis-ichthyosis-deafness syndrome, Noonan syndrome, Porokeratosis, Hearing loss with stapes fixation, Psoriasis, Senter syndrome, Skin neoplasms, Vohwinkel syndrome, Xeroderma, X-linked hearing loss with perilymphatic gusherView all (10 more) |
5195
|
|
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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, Peripheral neuropathy with sensorineural hearing impairment syndrome, Skin diseaseView all (2 more) |
5196
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|
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Gap junction protein beta 4 |
CX30.3, EKV, EKVP2 |
|
5197
|
|
|
Gap junction protein beta 5 |
CX31.1 |
|
5198
|
|
|
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, Hearing loss with stapes fixation, Senter syndrome, X-linked hearing loss with perilymphatic gusherView all (3 more) |
5199
|
|
|
Gap junction protein beta 7 |
CX25, bA136M9.1, connexin25 |
|
5200
|
|
|
Gap junction protein gamma 1 |
CX45, GJA7 |
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