Genes | GeDiPNet - Gene Disease Pathway & Associations

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14141 to 14150 of 15448 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
14141	7249	TSC2	TSC complex subunit 2	LAM, PPP1R160, TSC4	Autism, Polycystic kidney disease with tuberous sclerosis, Brain disease, Squamous cell carcinoma, Congenital neurologic anomalies, Cryptogenic west syndrome, Cystic fibrosis, Vascular dementia, Epilepsy, Adenomatous polyposis, Focal cortical dysplasia, Intellectual developmental disorder, Kidney neoplasms, Leiomyoma, Myeloid leukemia View all (14 more)
14142	8848	TSC22D1	TSC22 domain family member 1	HUCEP-2, Ptg-2, TGFB1I4, TSC22	Alzheimer disease, Anti-neutrophil antibody associated vasculitis, Carcinoma, Liver cirrhosis, Liver neoplasms, Oligodendroglioma, Scoliosis
14143	9819	TSC22D2	TSC22 domain family member 2	TILZ4a, TILZ4b, TILZ4c	Keratoconus, Moyamoya disease, Nephrotic syndrome
14144	1831	TSC22D3	TSC22 domain family member 3	DIP, DSIPI, GILZ, TSC-22R	Hyperinsulinism, Male infertility, Testicular disease
14145	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
14146	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)
14147	79042	TSEN34	TRNA splicing endonuclease subunit 34	LENG5, PCH2C, SEN34, SEN34L	Deglutition disorder, Intellectual developmental disorder, Microcephaly, Movement disorder, Obesity, Pontocerebellar hypoplasia, Visual disorder
14148	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
14149	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
14150	80705	TSGA10	Testis specific 10	CEP4L, CT79, SPGF26	Spermatogenic failure, Uterine fibroid

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