Genesⓘ

Dataset:
? Reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "T"
91 to 100 of 913 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

91
Transmembrane channel like 6
EV1, EVER1, EVIN1, LAK-4P, TNRC6C-AS1, lnc
Diabetes mellitus, Epidermodysplasia verruciformis, Diabetes mellitus, type 2

92
Twinfilin actin binding protein 2
A6RP, A6r, MSTP011, PTK9L
Autism, Bipolar disorder, Colorectal cancer, Colonic neoplasm, Diverticular disease, Osteoarthritis, Schizophrenia

93
Tubulin alpha 3d
H2-ALPHA, KTCN9, TUBA2
Keratoconus

94
Target of EGR1, exonuclease
PCH7, TOE-1, hCaf1z
Congenital brain malformation, Congenital pontocerebellar hypoplasia, Hydranencephaly, Lissencephaly, Macrogyria, Microgyria, Pontocerebellar hypoplasia

95
Tripartite motif containing 9
RNF91, SPRING
Alzheimer disease, Gastroesophageal reflux disease, Orofacial cleft, Psychotic disorders, Schizophrenia, Scoliosis

96
TIR domain containing adaptor protein
BACTS1, Mal, MyD88-2, wyatt
Prostatic neoplasm, Severe acute respiratory syndrome, Tuberculoma, Tuberculosis

97
Transmembrane protein 132B
-
Alzheimer disease, Attention deficit hyperactivity disorder, Bipolar disorder, Dementia, Major depressive disorder, Melanoma, Nonalcoholic fatty liver disease, Obstructive sleep apnea syndrome, Psychiatric disorders, Amyotrophic lateral sclerosis, Substance abuse, Diabetes mellitus, type 2

98
TNF receptor superfamily member 13C
BAFF-R, BAFFR, BROMIX, CD268, CVID4, prolixin
Brain injuries, Common variable immunodeficiency

99
TRNA splicing endonuclease subunit 15
C1orf19, PCH2F, sen15
Color vision deficiency, Congenital myasthenic syndrome, Global developmental delay, Open angle glaucoma, Osteoarthritis, Pontocerebellar hypoplasia, Prostate cancer, Scoliosis, Diabetes mellitus, type 2

100
Thioesterase superfamily member 4
CTMP
Atrial fibrillation, Hepatocellular carcinoma, Digestive system disease, Diverticular disease