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
Showing genes starting with "G"
241 to 250 of 677 Genes
Show
Entrez ID Gene Symbol Gene Name Synonyms Diseases

241
GIPC PDZ domain containing family member 2
SEMCAP-2, SEMCAP2
Bipolar disorder, Brain infarction, Kidney disease, Congestive heart failure, Crohn disease, Melanoma, Heart failure, Hodgkin lymphoma, Hypertrophic cardiomyopathy, Idiopathic pulmonary fibrosis, Inflammatory bowel disease, Insomnia, Lung cancer, Metabolic syndrome, Obesity
View all (7 more)

242
GIPC PDZ domain containing family member 3
C19orf64, DFNB15, DFNB72, DFNB95
Alzheimer disease, Isolated sensorineural deafness, Nonsyndromic hearing loss, Deafness, Hearing impairment, Hearing loss

243
Gastric inhibitory polypeptide receptor
PGQTL2
Alzheimer disease, Bladder calculus, Body weight, Breast cancer, Non-small-cell lung carcinoma, Cardiovascular disease, Cervical cancer, Cholecystolithiasis, Coronary artery disease, Diabetes mellitus, Diabetic retinopathy, Estrogen-receptor negative breast cancer, Gallstones, Heart failure, Metabolic syndrome
View all (8 more)

244
GIT ArfGAP 1
p95-APP1
Attention deficit hyperactivity disorder, Developmental disability, Hyperkinesia, Memory disorders

245
GIT ArfGAP 2
CAT-2, CAT2, PKL
Cardiovascular disease, Inflammatory bowel disease, Metabolic syndrome, Diabetes mellitus type 2

246
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 (21 more)

247
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

248
Gap junction protein alpha 4
CX37
Ischemic heart disease, Coronary artery disease, Hemangiosarcoma, Hypertension, Liver cirrhosis, Myocardial infarction, Myocardial ischemia

249
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)

250
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)