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"
1011 to 1020 of 1185 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1011
TRNA splicing endonuclease subunit 54
PCH2A, PCH4, PCH5, SEN54L, sen54
Amblyopia, Cerebellar hypoplasia/atrophy, epilepsy, and global developmental delay, Obstructive pulmonary disease, Congenital neurologic anomalies, Deglutition disorder, Global developmental delay, Intellectual developmental disorder, Methylmalonic acidemia, Microcephaly, Movement disorder, Pontocerebellar hypoplasia, Visual disorder

1012
Ts translation elongation factor, mitochondrial
EFTS, EFTSMT
Dilated cardiomyopathy, Combined oxidative phosphorylation deficiency, Skeletal muscle disorder, Dyskinesia, Gout, Leigh syndrome, Mitochondrial disease, Multiple sclerosis, Nephrotic syndrome, Sarcoidosis, Steroid-resistant nephrotic syndrome

1013
Testis specific 10
CEP4L, CT79, SPGF26
Spermatogenic failure, Uterine fibroid

1014
Testis specific 10 interacting protein
FAM161C
Breast cancer, Gout, Multiple sclerosis, Non-melanoma skin carcinoma, Open angle glaucoma

1015
Testis specific 13
-
Osteonecrosis

1016
Thyroid stimulating hormone subunit beta
TSH-B, TSH-BETA
Bipolar disorder, Thyroid agenesis, Congenital thyroid atrophy, Congenital hypothyroidism, Congenital hypothyroidism without goiter, Bipolar depression, Graves disease, Hypothyroidism

1017
Thyroid stimulating hormone receptor
CHNG1, LGR3, hTSHR-I
Antiphospholipid syndrome, Congenital hypothyroidism, Autoimmune thyroid disease, Bladder exstrophy and epispadias complex, Carcinoma, Cardiomyopathy, Thyroid agenesis, Congenital thyroid atrophy, Congenital hypothyroidism due to absence of thyroid gland, Congenital hypothyroidism without goiter, Congestive ophthalmopathy, Developmental delay, Epilepsy, Hyperthyroidism, Graves disease
View all (11 more)

1018
Teashirt zinc finger homeobox 1
CAA, NY-CO-33, SDCCAG33, TSH1
Alzheimer disease, Anorexia nervosa, Congenital aural atresia, Colonic neoplasms, Color vision deficiency, Colorectal cancer, Congenital external auditory canal atresia, Congenital vertical talus, Dementia, Eating disorder, Endometrial neoplasms, Prostate cancer

1019
Teashirt zinc finger homeobox 2
C20orf17, OVC10-2, TSH2, ZABC2, ZNF218
Alzheimer disease, Attention deficit hyperactivity disorder, Bipolar disorder, Coronary aneurysm, Crohn disease, Dementia, Dry eye syndrome, Inflammatory bowel disease, Major depressive disorder, Scoliosis, Substance abuse, Diabetes mellitus type 2

1020
Teashirt zinc finger homeobox 3
TSH3, ZNF537
Attention deficit hyperactivity disorder, Autism, Congenital anomalies of the kidney and urinary tract, Obstructive pulmonary disease, Congenital anomalies of kidney and urinary tract, Corneal astigmatism, Generalized anxiety disorder, Hyperopia, Neurodevelopmental disorder, Peripheral arterial disease, Substance abuse, Diabetes mellitus type 2