Genesⓘ

Dataset:
? Reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "T"
861 to 870 of 913 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

861
Tetraspanin 18
TSPAN
Colorectal cancer, Intellectual developmental disorder, Obstructive sleep apnea syndrome, Open angle glaucoma, Schizophrenia

862
TATA-box binding protein associated factor, RNA polymerase I subunit A
MGC:17061, RAFI48, SL1, TAFI48
Cardiomyopathy, Coronary artery disease, Dilated cardiomyopathy, Hypertension

863
THAP domain containing 3
-
Polycystic ovary syndrome

864
TOPBP1 interacting checkpoint and replication regulator
C15orf42, SLD3, Treslin
Atrial fibrillation, Hepatocellular carcinoma, Obstructive pulmonary disease, Hypertension, Multiple myeloma, Obesity

865
Transmembrane protein 263
C12orf23
Kawasaki disease

866
Transducin beta like 1 Y-linked
DFNY2, TBL1
Autism, Deafness, y-linked

867
TENM3 antisense RNA 1
TENM3-AS2

868
T-box transcription factor 19
TBS19, TPIT, dJ747L4.1
Major depressive disorder, Gastroenteritis, Depression, Pituitary stalk interruption syndrome

869
T-box transcription factor 18
CAKUT2, PUJO
Androgenetic alopecia, Anophthalmia, Breast cancer, Congenital anomalies of the kidney and urinary tract, Cardiac embolism, Cardioembolic stroke, Carpal tunnel syndrome, Central nervous system cancer, Kidney disease, Renal agenesis, Congenital anomalies of kidney and urinary tract, Glioblastoma, Glioma, Hypertension, Immune system disease
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870
Transmembrane protein 67
JBTS6, MECKELIN, MKS3, NPHP11, TNEM67
Anhydramnios, Hemolytic uremic syndrome, Bardet-biedl syndrome, Boichis syndrome, Cerebellar malformation, Ciliopathies, Coach syndrome, Congenital neurologic anomalies , Congenital ocular coloboma, Cystic kidney disease, Desbuquois syndrome, Aplasia of the vermis, Global developmental delay, Insomnia, Intellectual developmental disorder
View all (14 more)