Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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5181 to 5190 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

5181
Gastric inhibitory polypeptide
-
Anorexia, Coronary artery disease, Diabetes mellitus type 2, Diabetic neuropathy, Hypertension, Hyperlipidemia, Insomnia, Metabolic syndrome, Myocardial infarction, Obesity, Prostate cancer

5182
GIPC PDZ domain containing family member 1
C19orf3, GIPC, GLUT1CBP, Hs.6454, IIP-1, NIP, OPDM2, RGS19IP1, SEMCAP, SYNECTIIN, SYNECTIN, TIP-2
Bladder calculus, Nephrolithiasis, Oculopharyngodistal myopathy, Urolithiasis

5183
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)

5184
GIPC PDZ domain containing family member 3
C19orf64, DFNB15, DFNB72, DFNB95
Alzheimer disease, Isolated sensorineural deafness, Nonsyndromic hearing loss, Deafness, Hearing impairment, Hearing loss

5185
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)

5186
GIT ArfGAP 1
p95-APP1
Attention deficit hyperactivity disorder, Developmental disability, Hyperkinesia, Memory disorders

5187
GIT ArfGAP 2
CAT-2, CAT2, PKL
Cardiovascular disease, Inflammatory bowel disease, Metabolic syndrome, Diabetes mellitus type 2

5188
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)

5189
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

5190
Gap junction protein alpha 4
CX37
Ischemic heart disease, Coronary artery disease, Hemangiosarcoma, Hypertension, Liver cirrhosis, Myocardial infarction, Myocardial ischemia