Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "T"

1011 to 1020 of 1188 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
1011	116461	TSEN15	TRNA splicing endonuclease subunit 15	C1orf19, PCH2F, sen15	Color vision deficiency, Congenital microcephaly, Global developmental delay, Open angle glaucoma, Osteoarthritis, Pontocerebellar hypoplasia, Prostate cancer, Scoliosis, Diabetes mellitus type 2
1012	80746	TSEN2	TRNA splicing endonuclease subunit 2	PCH2B, SEN2, SEN2L	Alzheimer disease, Coronary artery disease, Deglutition disorder, Hemolytic uremic syndrome, Hypertrophic cardiomyopathy, Osteonecrosis of the femoral head, Intellectual developmental disorder, Metabolic syndrome, Microcephaly, Movement disorder, Nonalcoholic fatty liver disease, Periodontal disease, Periodontitis, Pontocerebellar hypoplasia, Systemic lupus erythematosus View all (3 more)
1013	79042	TSEN34	TRNA splicing endonuclease subunit 34	LENG5, PCH2C, SEN34, SEN34L	Deglutition disorder, Intellectual developmental disorder, Microcephaly, Movement disorder, Obesity, Pontocerebellar hypoplasia, Visual disorder
1014	283989	TSEN54	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
1015	10102	TSFM	Ts translation elongation factor, mitochondrial	EFTS, EFTSMT	Dilated cardiomyopathy, Combined oxidative phosphorylation deficiency, Disorder of skeletal muscle, Dyskinesia, Gout, Leigh syndrome, Mitochondrial disease, Multiple sclerosis, Nephrotic syndrome, Sarcoidosis, Steroid-resistant nephrotic syndrome
1016	80705	TSGA10	Testis specific 10	CEP4L, CT79, SPGF26	Spermatogenic failure, Uterine fibroid
1017	254187	TSGA10IP	Testis specific 10 interacting protein	FAM161C	Breast cancer, Gout, Multiple sclerosis, Non-melanoma skin carcinoma, Open angle glaucoma
1018	114960	TSGA13	Testis specific 13	-	Osteonecrosis
1019	7252	TSHB	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
1020	7253	TSHR	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)

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