Genes | GeDiPNet - Gene Disease Pathway & Associations

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14291 to 14300 of 15448 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
14291	11344	TWF2	Twinfilin actin binding protein 2	A6RP, A6r, MSTP011, PTK9L	Autism, Bipolar disorder, Colorectal cancer, Colonic neoplasms, Diverticular disease, Osteoarthritis, Schizophrenia
14292	7291	TWIST1	Twist family bHLH transcription factor 1	ACS3, BPES2, BPES3, CRS, CRS1, CSO, SCS, SWCOS, TWIST, bHLHa38	Androgenetic alopecia, Asthma, Atherosclerosis, Atrial fibrillation, Brachycephaly, Cardiovascular disease, Central nervous system cancer, Cerebrovascular disorder, Ischemic heart disease, Obstructive pulmonary disease, Colorectal cancer, Coronal craniosynostosis, Coronary artery disease, Craniosynostosis, Desbuquois syndrome View all (16 more)
14293	117581	TWIST2	Twist family bHLH transcription factor 2	AMS, BBRSAY, DERMO1, FFDD3, SETLSS, bHLHa39	Ablepharon macrostomia syndrome, Alzheimer disease, Androgenetic alopecia, Barber-say syndrome, Congenital ectodermal dysplasia of face, Dry eye syndrome, Focal facial dermal dysplasia, Peptic ulcer disease, Sjogren syndrome
14294	56652	TWNK	Twinkle mtDNA helicase	ATXN8, C10orf2, IOSCA, MTDPS7, PEO, PEO1, PEOA3, PRLTS5, SANDO, SCA8, TWINL	Auditory neuropathy, Progressive external ophthalmoplegia, Cerebellar ataxia, Ptosis, Atrioventricular block, Mitochondrial dna depletion syndrome, Major depressive disorder, Dysphonia, Gonadal dysgenesis, Mitochondrial disease, Mitochondrial hepatopathy, Perrault syndrome, Nonsyndromic hearing loss, Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis, Hereditary spastic paraplegia, Xx gonadal dysgenesis syndrome View all (1 more)
14295	57045	TWSG1	Twisted gastrulation BMP signaling modulator 1	TSG	Esophageal squamous cell carcinoma, Holoprosencephaly
14296	7294	TXK	TXK tyrosine kinase	BTKL, PSCTK5, PTK4, RLK, TKL	Breast cancer, Multiple sclerosis
14297	167838	TXLNB	Taxilin beta	C6orf198, LST001, MDP77, dJ522B19.2	Obesity
14298	7295	TXN	Thioredoxin	TRDX, TRX, TRX1, TXN1, Trx80	Breast neoplasms, Bronchopulmonary dysplasia, Cardiomyopathy, Congenital abnormalities, Contact dermatitis, Gout, Hydrocephalus, Alzheimer disease, Liver disease, Mesothelioma, Pelvic organ prolapse
14299	25828	TXN2	Thioredoxin 2	COXPD29, MT-TRX, MTRX, TRX2, TXN	Combined oxidative phosphorylation deficiency
14300	51061	TXNDC11	Thioredoxin domain containing 11	EFP1	Rheumatoid arthritis

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