Genes | GeDiPNet - Gene Disease Pathway & Associations

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1631 to 1640 of 12229 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
1631	116	ADCYAP1	Adenylate cyclase activating polypeptide 1	PACAP	Bipolar disorder, Cardiomyopathy, Clonic seizures, Esophagus neoplasm, Hyperemia, Hypotonic seizures, Jacksonian seizure, Mental depression, Miosis disorder, Myocardial diseases, Schizophrenia, Seizure
1632	116028	RMI2	RecQ mediated genome instability 2	BLAP18, C16orf75	Ankylosing spondylitis, Arthritis, Asthma, Autoimmune diseases, Celiac disease, Cholangitis, Crohn disease, Diabetes mellitus, Eczema, Immune system diseases, Inflammatory bowel disease, Intrauterine growth restriction, congenital multiple caf -au-lait macules-increased sister chromatid exchange syndrome, Leprosy, Multiple sclerosis, Oligoarticular arthritis View all (9 more)
1633	116039	OSR2	Odd-skipped related transciption factor 2	-	Endometrioma, Endometriosis
1634	116071	BATF2	Basic leucine zipper ATF-like transcription factor 2	SARI	Melanoma
1635	116085	SLC22A12	Solute carrier family 22 member 12	OAT4L, RST, UAT, URAT1, hURAT1	Acute kidney insufficiency, Gout, Gouty arthritis, Hereditary renal hypouricemia, Hyperuricemia, Kidney failure, Renal hypouricemia, Renal tubular necrosis, Uric acid renal calculus, Uric acid urolithiasis
1636	1161	ERCC8	ERCC excision repair 8, CSA ubiquitin ligase complex subunit	CKN1, CSA, UVSS2	Anhidrosis, Cataract, Cerebellar ataxia, Cerebellar atrophy, Cerebral atrophy, Cockayne syndrome, Congenital pes cavus, Congestive heart failure, Cryptorchidism, Dementia, Dysarthria, Hearing loss, Hydrocephalus, Hyperopia, Hypertension View all (15 more)
1637	116113	FOXP4	Forkhead box P4	hFKHLA	Breast cancer, Developmental delay, Laryngeal hypoplasia, Prostatic neoplasms, Prostate cancer, Ventricular septal defect
1638	116115	ZNF526	Zinc finger protein 526	DENNED	Mental retardation, Pulmonary stenosis
1639	116135	LRRC3B	Leucine rich repeat containing 3B	LRP15	Breast cancer, Mammary neoplasms, Breast carcinoma, Colorectal cancer, Colorectal neoplasms, Gastric cancer, Leukemia, Marfan syndrome, Stomach neoplasms
1640	116150	NUS1	NUS1 dehydrodolichyl diphosphate synthase subunit	C6orf68, CDG1AA, MGC:7199, MRD55, NgBR, TANGO14	Attention deficit hyperactivity disorder, Autism, Cerebral atrophy, Cerebral cortical atrophy, Congenital disorder of glycosylation, Developmental delay, Developmental regression, Diabetes mellitus, Dwarfism, Dyskinetic syndrome, Epileptic encephalopathy, Gastroesophageal reflux disease, Hypertrichosis, Hypodontia, Melanoma View all (9 more)

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