Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "T"

981 to 990 of 1188 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
981	7222	TRPC3	Transient receptor potential cation channel subfamily C member 3	SCA41, TRP3	Asthma, Spinocerebellar ataxia, Atrial fibrillation, Bipolar disorder, Bipolar depression, Hypertension, Non-small cell lung carcinoma, Squamous cell carcinoma
982	7223	TRPC4	Transient receptor potential cation channel subfamily C member 4	HTRP-4, HTRP4, TRP4	Attention deficit hyperactivity disorder, Autism, Obesity, Obsessive-compulsive disorder, Schizophrenia, Substance abuse, Tourette syndrome
983	26133	TRPC4AP	Transient receptor potential cation channel subfamily C member 4 associated protein	C20orf188, PPP1R158, TRRP4AP, TRUSS	Angioedema, Basal cell carcinoma, Biliary tract cancer, Breast cancer, Cancer, Cervical cancer, Colorectal cancer, Coronary artery disease, Cutaneous squamous cell carcinoma, Endometrial cancer, Esophageal cancer, Estrogen-receptor negative breast cancer, Gastric cancer, Hepatocellular carcinoma, Hypothyroidism View all (11 more)
984	7224	TRPC5	Transient receptor potential cation channel subfamily C member 5	PPP1R159, TRP5	Hypertension, Intellectual developmental disorder, Neurodevelopmental disorder, Non-melanoma skin carcinoma
985	7225	TRPC6	Transient receptor potential cation channel subfamily C member 6	FSGS2, TRP6	Alzheimer disease, Cardiac embolism, Cardioembolic stroke, Fatigue syndrome, Colorectal adenoma, Colorectal cancer, Idiopathic steroid-resistant nephrotic syndrome, Focal glomerulosclerosis, Focal segmental glomerulosclerosis, Genetic steroid-resistant nephrotic syndrome, Hereditary steroid-resistant nephrotic syndrome, Hypertension, Hypertrophy, Nephrotic syndrome, Kidney disease View all (3 more)
986	57113	TRPC7	Transient receptor potential cation channel subfamily C member 7	TRP7	Bipolar disorder, Insomnia, Peripheral neuropathy
987	4308	TRPM1	Transient receptor potential cation channel subfamily M member 1	CSNB1C, LTRPC1, MLSN1	Alzheimer disease, Angioedema, Atrophic macular degeneration, Colorectal cancer, Congenital stationary night blindness, Esophageal cancer, Gastric cancer, Huntington disease, Immune system disease, Intellectual developmental disorder, Myasthenia gravis, Night blindness, congenital stationary, Oguchi disease, Optic atrophy, Retinitis pigmentosa View all (3 more)
988	7226	TRPM2	Transient receptor potential cation channel subfamily M member 2	EREG1, KNP3, LTRPC2, LTrpC-2, NUDT9H, NUDT9L1, TRPC7	Anorectal malformation, Atrial fibrillation, Bipolar disorder, Bipolar depression, Disturbance in mood, Non-organic psychosis, Ovarian diseases, Parkinson disease, Psychotic disorders
989	80036	TRPM3	Transient receptor potential cation channel subfamily M member 3	CTRCT50, GON-2, LTRPC3, MLSN2, NEDFSS	Amphetamine or sympathomimetic abuse, Atrophic macular degeneration, Nonsyndromic intellectual disability, Bipolar disorder, Birk-barel syndrome, Cataract, Cataract-glaucoma syndrome, Central nervous system cancer, Color vision deficiency, Coronary artery disease, Crohn disease, Developmental and epileptic encephalopathy, Glioblastoma, Glioma, Global developmental delay View all (17 more)
990	54795	TRPM4	Transient receptor potential cation channel subfamily M member 4	EKVP6, LTrpC4, PFHB1B, TRPM4B, hTRPM4	Alzheimer disease, Arrhythmogenic right ventricular cardiomyopathy, Atrioventricular block, Brugada syndrome, Cardiac arrest, Cardiac conduction disease, Cardiomyopathy, Dilated cardiomyopathy, Conduction disorder of the heart, Congestive heart failure, Erythrokeratodermia variabilis, Heart failure, Hereditary bundle branch system defect, Hypertrophic cardiomyopathy, Long qt syndrome View all (5 more)

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