GeDiPNet Database: Explore Human Gene Data, Disease Associations & Pathway Insights

Home
Browse
- Genes
- Diseases
- Pathways
  - Reactome
  - KEGG
Analysis
Help
Links
FAQ
Contact us

Dataset: Curated All	Genes	Show
		Search by alphabet

1 to 10 of 12229 Genes

	Entrez ID	Gene symbol	Gene name	Synonyms	Diseases
	1	A1BG	Alpha-1-B glycoprotein	A1B, ABG, GAB, HYST2477	Schizophrenia
	10	NAT2	N-acetyltransferase 2	AAC2, NAT-2, PNAT	Acrania, Anencephaly, Urinary bladder cancer, Bladder neoplasm, Breast cancer, Mammary neoplasms, Breast carcinoma, Coronary arteriosclerosis, Coronary artery disease, Craniorachischisis, Dermatitis, Diastematomyelia, Industrial dermatosis, Lymphoblastic leukemia, Leukopenia, Liver neoplasms, Liver cancer, Liver carcinoma, Malignant mesothelioma, Marfan syndrome, Neural tube defect, Neurenteric cyst, Primary tethered cord syndrome, Prostatic neoplasms, Prostate cancer, Spinal cord myelodysplasia
	100	ADA	Adenosine deaminase	ADA1	Adenosine deaminase deficiency, Alopecia, Anemia, Asthma, Autism, Autoimmune hemolytic anemia, B-cell lymphoma, Aplasia of the thymus, Dermatitis, Eosinophilia, Exfoliative dermatitis, Hyperemia, Hypothyroidism, Immune thrombocytopenic purpura, Lung neoplasms, Lung cancer, Lymphoma, Mesangial sclerosis, Multiple gastrointestinal atresias, Nephrotic syndrome, Omenn syndrome, Otitis media, Pancreatic adenocarcinoma, Severe combined immunodeficiency disease, Sinusitis, Spinal cord diseases, Thyroiditis
	1000	CDH2	Cadherin 2	ACOGS, ADHD8, ARVD14, CD325, CDHN, CDw325, NCAD	Arrhythmogenic right ventricular cardiomyopathy, Breast cancer, Mammary neoplasms, Breast carcinoma, Developmental delay, Duane retraction syndrome, Gastric cancer, Grand mal status epilepticus, Malformation of cortical development, Marfan syndrome, Mental retardation, Mirror movements, Myocardial ischemia, Nonconvulsive status epilepticus, Petit mal status, Status epilepticus, Stomach neoplasms
	10000	AKT3	AKT serine/threonine kinase 3	MPPH, MPPH2, PKB-GAMMA, PKBG, PRKBG, RAC-PK-gamma, RAC-gamma, STK-2	Central nervous system neoplasms, Cortical dysplasia, Cutis marmorata, Developmental delay, Dysmorphic features, Glioblastoma, Glioma, Hemimegalencephaly, Hydrocephalus, Hypoplasia of corpus callosum, Macrocephaly, Malformation of cortical development, Megalanecephaly polymicrogyria-polydactyly hydrocephalus syndrome, Megalencephaly cutis marmorata telangiectatica congenita, Megalencephaly, polymicrogyria, polydactyly, hydrocephalus syndrome, Melanoma, Mental retardation, Microstomia, Polydactyly, Polymicrogyria, Postaxial hand polydactyly, Schizophrenia, Strawberry nevus of skin, Ventricular septal defect
	10002	NR2E3	Nuclear receptor subfamily 2 group E member 3	ESCS, PNR, RNR, RP37, rd7	Cataract, Color blindness, Cone-rod dystrophy, Congenital hypoplasia of penis, Cystoid macular retinal degeneration, Diabetes mellitus, Disorder of eye, Enhanced s-cone syndrome, Glaucoma, Goldmann-favre syndrome, Hearing loss, Hemeralopia, Horizontal nystagmus, Hyperinsulinism, Hypogonadism, Keratoconus, Leber congenital amaurosis, Macular edema, Mental retardation, Nyctalopia, Nystagmus, Obesity, Optic atrophy, Retinal dystrophy, Retinitis pigmentosa, Retinoschisis, Rod-cone dystrophy, Vitreoretinal degeneration
	100033413	SNORD116-1	Small nucleolar RNA, C/D box 116-1	HBII-85-1, PWCR1	Acromicria, Acromicric dysplasia, Attention deficit hyperactivity disorder, Clinodactyly, Cryptorchidism, Developmental delay, Dolichocephaly, Dwarfism, Hyperinsulinism, Hyperopia, Hypogonadotropic hypogonadism, Isolated somatotropin deficiency, Motor delay, Hypotonia, Penis agenesis, Physiologic amenorrhea, Prader-willi syndrome, Royer syndrome, Scoliosis, Sleep apnea, Somatotropin deficiency, Specific learning disorder
	10004	NAALADL1	N-acetylated alpha-linked acidic dipeptidase like 1	HILAP, I100, NAALADASEL	Retinitis pigmentosa
	100048903	MCCD1P1	Mitochondrial coiled-coil domain 1 pseudogene 1	-	Lung carcinoma
	100048908	ZDHHC20P2	ZDHHC20 pseudogene 2	-	Cholangitis, Chronic obstructive pulmonary disease, Rheumatoid arthritis

| © 2021, Biomedical Informatics Centre, NIRRH |
ICMR-National Institute for Research in Reproductive Health, Jehangir Merwanji Street, Parel, Mumbai-400012
Tel: +91-22-24192104, Fax No: +91-22-24139412