Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
All A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
5161 to 5170 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

5161
GIT ArfGAP 1
p95-APP1
Attention deficit hyperactivity disorder, Developmental disability, Hyperkinesia, Memory disorders

5162
GIT ArfGAP 2
CAT-2, CAT2, PKL
Cardiovascular disease, Inflammatory bowel disease, Metabolic syndrome, Diabetes mellitus type 2

5163
Gap junction protein alpha 1
AVSD3, CMDR, CX43, EKVP, EKVP3, GJAL, HLHS1, HSS, ODDD, PPKCA
Anhedonia, Cardiac arrhythmias, Atrial fibrillation, Atrioventricular septal defect, Autism, Palmoplantar keratoderma with congenital alopecia, Bilateral microphthalmos, Breast neoplasms, Cardiac arrhythmia, Obstructive pulmonary disease, Cleft lip, Congenital heart disease, Coronary aneurysm, Craniometaphyseal dysplasia, Syndactyly
View all (20 more)

5164
Gap junction protein alpha 3
CTRCT14, CX46, CZP3
Cataract, Congenital cataract, Congenital cataract facial dysmorphism neuropathy syndrome, Nuclear cataract, Posterior polar cataract, Posterior subcapsular cataract

5165
Gap junction protein alpha 4
CX37
Ischemic heart disease, Coronary artery disease, Hemangiosarcoma, Hypertension, Myocardial infarction, Myocardial ischemia

5166
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
View all (1 more)

5167
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
View all (1 more)

5168
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
View all (5 more)

5169
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
View all (10 more)

5170
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)