Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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Showing genes starting with "T"
981 to 990 of 1185 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

981
Transient receptor potential cation channel subfamily C member 5
PPP1R159, TRP5
Hypertension, Intellectual developmental disorder, Neurodevelopmental disorder, Non-melanoma skin carcinoma

982
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)

983
Transient receptor potential cation channel subfamily C member 7
TRP7
Bipolar disorder, Insomnia, Peripheral neuropathy

984
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)

985
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

986
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)

987
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)

988
Transient receptor potential cation channel subfamily M member 6
CHAK2, HMGX, HOMG, HOMG1, HSH
Alzheimer disease, Magnesium metabolism disorder, Female infertility, Gout, Intestinal hypomagnesemia, Nephrolithiasis, Rod-cone dystrophy, Schizophrenia

989
Transient receptor potential cation channel subfamily M member 7
ALSPDC, CHAK, CHAK1, LTRPC7, LTrpC-7, TRP-PLIK
Amyotrophic lateral sclerosis, Macrothrombocytopenia, Central nervous system cancer, Colonic polyps, Colorectal neoplasms, Coronary artery disease, Immune system disorder, Glioblastoma, Glioma, Immune system disease, Liver cirrhosis, Paralysis, Parkinson-dementia complex of guam

990
Transient receptor potential cation channel subfamily M member 8
LTRPC6, LTrpC-6, TRPP8, trp-p8
Asthma, Eczema, Brain aneurysm, Common migraine, Melanoma, Migraine, Amyotrophic lateral sclerosis