Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "T"

741 to 750 of 913 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
741	79725	THAP9	THAP domain containing 9	hTh9	Cardiovascular disease
742	79736	TEFM	Transcription elongation factor, mitochondrial	C17orf42, COXPD58	Breast cancer, Combined oxidative phosphorylation deficiency, Lung cancer
743	79770	TXNDC15	Thioredoxin domain containing 15	BUG, C5orf14, MKS14, TMX5, UNQ335	Ciliopathies, Meckel syndrome, Meckel-gruber syndrome, Parkinson disease, Severe combined immunodeficiency, Diabetes mellitus, type 2
744	7980	TFPI2	Tissue factor pathway inhibitor 2	PP5, REF1, TFPI-2	Rheumatoid arthritis, Breast neoplasm, Hepatocellular carcinoma, Colorectal neoplasm, Liver cirrhosis, Melanoma, Osteoarthritis, Pancreatic neoplasm
745	79809	TTC21B	Tetratricopeptide repeat domain 21B	ATD4, CFAP60, FAP60, FLA17, IFT139, IFT139B, JBTS11, NPHP12, Nbla10696, SRTD4, THM1	Jeune syndrome, Attention deficit hyperactivity disorder, Autism, Bardet-biedl syndrome, Connective tissue disease, Desbuquois syndrome, Diabetic neuropathy, Epilepsy, Aplasia of the vermis, Jeune thoracic dystrophy, Joubert syndrome, Kidney disease, Majewski syndrome, Nephronophthisis, Nephrotic syndrome View all (2 more)
746	79816	TLE6	TLE family member 6, subcortical maternal complex member	GRG6, OZEMA15, PREMBL	Female infertility, Oligodendroglioma, Oocyte maturation defect
747	79838	TMC5	Transmembrane channel like 5	-	Alzheimer disease, Blood coagulation disorder, Parkinson disease
748	79853	TM4SF20	Transmembrane 4 L six family member 20	PRO994, SLI5, TCCE518	Specific language disorder
749	79867	TCTN2	Tectonic family member 2	C12orf38, JBTS24, MKS8, TECT2	Cystic kidney disease, Desbuquois syndrome, Aplasia of the vermis, Joubert syndrome, Meckel syndrome, Meckel-gruber syndrome
750	79875	THSD4	Thrombospondin type 1 domain containing 4	AAT12, ADAMTSL-6, ADAMTSL6, FVSY9334, PRO34005	Alzheimer disease, Aortic aneurysm, Asthma, Autism, Bipolar disorder, Breast cancer, Obstructive pulmonary disease, Color vision deficiency, Colorectal cancer, Congenital contractural arachnodactyly, Coronary artery disease, Dental caries, Estrogen-receptor negative breast cancer, Thoracic aortic aneurysm and aortic dissection, Iga nephropathy View all (10 more)

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