Genesⓘ

Dataset:
? Reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "T"
81 to 90 of 913 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

81
DNA topoisomerase II binding protein 1
Dpb11, TOP2BP1
Lymphocytic b-cell leukemia, Oligodendroglioma, Pulmonary arterial hypertension

82
Tripartite motif containing 31
C6orf13, HCG1, HCGI, RNF
Asthma, Autism, Autoimmune thyroid disease, Breast cancer, Obstructive pulmonary disease, Irritant dermatitis, Hepatocellular carcinoma, Insomnia, Major depressive disorder, Non-melanoma skin carcinoma, Prostate cancer, Psoriasis, Schizophrenia, Systemic lupus erythematosus, Diabetes mellitus, type 1

83
Tubulin polymerization promoting protein
TPPP/p25, TPPP1, p24, p25, p25alpha
Barrett esophagus, Brugada syndrome, Kidney disease, Depression, Esophageal adenocarcinoma, Hemorrhoid, Hypothyroidism, Kidney failure, Osteoarthritis, Peptic ulcer disease

84
TRIO and F-actin binding protein
DFNB28, HRIHFB2122, TAP68, TARA, dJ37E16.4
Atrial fibrillation, Attention deficit hyperactivity disorder, Autism, Isolated sensorineural deafness, Nonsyndromic hearing loss, Deafness, Glaucoma, Hearing impairment, Hearing loss, Meniere disease, Nephrolithiasis, Open angle glaucoma, Osteoarthritis

85
TBC1 domain family member 8
AD3, GRAMD8, HBLP1, TBC1D8A, VRP
Gout, Osteoporosis, Progressive supranuclear palsy, Rheumatoid arthritis

86
Trehalase
TRE, TREA, TREHD

87
TP53 target 1
LINC00096, NCRNA00096, P53TG1, P53TG1-D, TP53AP1, TP53LC12

88
Tubulin alpha 3e
-
Neurodevelopmental disorder, Congenital myasthenic syndrome, Global developmental delay, Lissencephaly, Neurodevelopmental disorders, Non-specific syndromic intellectual disability

89
Three prime repair exonuclease 1
AGS1, CRV, DRN3, HERNS, RVCLS
Aicardi goutieres syndrome, Brain disease, Cadasil, Chilblain lupus erythematosus, Vascular dementia, Chilblain lupus, Systemic lupus erythematosus, Neurodevelopmental disorders, Obesity, Retinitis pigmentosa

90
TP53 regulating kinase
BUD32, C20orf64, GAMOS4, Nori-2, Nori-2p, PRPK, TPRKB, dJ101A2
Galloway-mowat syndrome, Global developmental delay