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"
641 to 650 of 1185 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

641
Transmembrane inner ear
DFNB6
Isolated sensorineural deafness, Nonsyndromic hearing loss, Color vision deficiency, Congenital ear anomaly, Deafness, Hearing impairment, Hearing loss, Hereditary hearing loss

642
Transmembrane and immunoglobulin domain containing 3
AD026
Autism, Scoliosis, Stomatitis

643
Trimethyllysine hydroxylase, epsilon
AUTSX6, BBOX2, TMLD, TMLH, TMLHED, XAP130
Autism, Autism, x-linked, Cerebellar hypoplasia/atrophy, epilepsy, and global developmental delay, Intellectual developmental disorder, Schizophrenia, Venous thromboembolism

644
Tropomodulin 1
D9S57E, ETMOD, TMOD
Alzheimer disease, Barrett esophagus, Brain aneurysm, Dilated cardiomyopathy, Esophageal adenocarcinoma, Obesity, Ovarian cysts, Cardiomyopathy, Prostatic neoplasms

645
Tropomodulin 3
UTMOD
Attention deficit hyperactivity disorder, Autism

646
Tropomodulin 4
SK-TMOD
Kidney disease, Coronary artery disease, Hypertension, Myocardial infarction, Stroke

647
Thymopoietin
CMD1T, LAP2, LEMD4, PRO0868, TP
Aortic aneurysm, Rheumatoid arthritis, Arthrogryposis multiplex congenita, Dilated cardiomyopathy, Cardiomyopathy, Hypertrophic cardiomyopathy, Long qt syndrome, Myocardial ischemia, Pena-shokeir syndrome

648
Transmembrane protein with metallophosphoesterase domain
-
Gm1 gangliosidosis, Mucopolysaccharidosis

649
Transmembrane serine protease 11A
ECRG1, HATL1, HESP
Dementia

650
Transmembrane serine protease 11B
HATL5
Obesity, Venous thromboembolism