Genes | GeDiPNet - Gene Disease Pathway & Associations

Dataset:

All A B C D E F G H I J K L M N O P Q R S T U V W X Y Z

Showing genes starting with "T"

61 to 70 of 1188 Genes

Show

	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
61	57551	TAOK1	TAO kinase 1	DDIB, KFC-B, MAP3K16, MARKK, PSK-2, PSK2, TAO1, hKFC-B, hTAOK1	Nonsyndromic intellectual disability, Neurodevelopmental disorder, Developmental delay with or without intellectual or behavioral abnormalities, Global developmental delay, Intellectual developmental disorder, Non-specific syndromic intellectual disability
62	9344	TAOK2	TAO kinase 2	MAP3K17, PSK, PSK1, PSK1-BETA, TAO1, TAO2, Tao2beta	Autism, Bipolar disorder, Insomnia, Metabolic syndrome, Neurodevelopmental disorder, Osteoarthritis, Schizophrenia, Diabetes mellitus type 2
63	51347	TAOK3	TAO kinase 3	DPK, JIK, MAP3K18, hKFC-A	Color vision deficiency, Major depressive disorder, Neurodevelopmental disorder, Neurotic disorder, Post-traumatic stress disorder, Systemic lupus erythematosus
64	6890	TAP1	Transporter 1, ATP binding cassette subfamily B member	ABC17, ABCB2, APT1, D6S114E, MHC1D1, PSF-1, PSF1, RING4, TAP1*0102N, TAP1N	Ankylosing spondylitis, Asthma, Autoimmune disease, Bare lymphocyte syndrome, Bronchiectasis, Celiac disease, Diabetes mellitus type 1, Diffuse cutaneous systemic sclerosis, Extrinsic allergic alveolitis, Glaucoma, Hypothyroidism, Myocardial ischemia, Prostatic neoplasms, Psoriasis, Rheumatoid arthritis View all (3 more)
65	6891	TAP2	Transporter 2, ATP binding cassette subfamily B member	ABC18, ABCB3, APT2, D6S217E, MHC1D2, PSF-2, PSF2, RING11	Alzheimer disease, Ankylosing spondylitis, Anorexia nervosa, Asthma, Attention deficit hyperactivity disorder, Autoimmune thyroid disease, Bare lymphocyte syndrome, Coronary artery disease, Dental caries, Allergic contact dermatitis, Diabetes mellitus type 1, Diffuse cutaneous systemic sclerosis, Erythematosquamous dermatosis, Gout, Hyperthyroidism View all (21 more)
66	6892	TAPBP	TAP binding protein	MHC1D3, NGS17, TAPA, TPN, TPSN	Bare lymphocyte syndrome, Interstitial cystitis, Rheumatoid arthritis, Schizophrenia, Severe combined immunodeficiency, Diabetes mellitus type 1
67	55080	TAPBPL	TAP binding protein like	TAPBP-R, TAPBPR	Ataxia, spastic, autosomal dominant, Myasthenic syndrome, Spastic paraplegia
68	202018	TAPT1	Transmembrane anterior posterior transformation 1	CMVFR, OCLSBG	Bone fragility with contractures, arterial rupture, and deafness, Cataract, Kidney disease, Osteochondrodysplasia, Desbuquois syndrome, Diabetic neuropathy, Osteoporosis-pseudoglioma syndrome, Scoliosis
69	6894	TARBP1	TRNA guanosine 2 -O-methyltransferase TARBP1	TRM3, TRMT3, TRP-185, TRP185	Hypertension, Oligodendroglioma, Systemic lupus erythematosus
70	23435	TARDBP	TAR DNA binding protein	ALS10, TDP-43	Amyotrophic lateral sclerosis, Androgenetic alopecia, Degenerative disorder, Frontotemporal dementia, Frontotemporal dementia with motor neuron disease, Masp2 deficiency, Motor neuron disease, Myositis, Neurodegenerative disorder, Parkinson disease

«««...5 678 9...»»»