Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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13131 to 13140 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

13131
Tetratricopeptide repeat, ankyrin repeat and coiled-coil containing 2
IDDALDS, ROLSA, rols
Autism, Developmental delay, Dyslexia, Epilepsy, Insomnia, Intellectual developmental disorder autism speech, Intellectual developmental disorder, Alzheimer disease, Neurodevelopmental disorder, Non-specific syndromic intellectual disability, Peripheral arterial disease, Prostate cancer, Schizophrenia

13132
Transport and golgi organization 2 homolog
C22orf25, MECRCN
Autism, Cardiac arrhythmia, Cardiovascular disease, Episodic ataxia, Global developmental delay, Intellectual developmental disorder, Scoliosis, Diabetes mellitus type 2

13133
Transport and golgi organization 6 homolog
TMCO7
Atrial fibrillation, Attention deficit hyperactivity disorder, Sclerosing cholangitis, Scoliosis

13134
TRAF family member associated NFKB activator
I-TRAF, ITRAF, TRAF2
Attention deficit hyperactivity disorder, Autism, Breast neoplasms, Cannabis abuse, Hypothyroidism, Insomnia, Major depressive disorder, Peripheral neuropathy, Substance abuse

13135
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

13136
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

13137
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

13138
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
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13139
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 (20 more)

13140
TAP binding protein
MHC1D3, NGS17, TAPA, TPN, TPSN
Bare lymphocyte syndrome, Interstitial cystitis, Rheumatoid arthritis, Schizophrenia, Severe combined immunodeficiency, Diabetes mellitus type 1