Genesⓘ

Dataset:
? Reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "T"
501 to 510 of 913 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

501
TATA-box binding protein associated factor 4
MRD73, TAF(II)130, TAF(II)135, TAF2C, TAF2C1, TAF4A, TAFII-130, TAFII-135, TAFII130, TAFII135
Color vision deficiency, Intellectual developmental disorder, Major depressive disorder, Neurodevelopmental disorders, Non-specific syndromic intellectual disability, Open angle glaucoma

502
TATA-box binding protein associated factor 4b
SPGF13, TAF2C2, TAFII105
Bell's palsy, Obstructive asthma, Male infertility single gene azoospermia, Spermatogenic failure

503
Transgelin
SM22, SM22-alpha, SMCC, TAGLN1, TGLN, WS3-10
Breast cancer, Cardiovascular disease, Colonic neoplasm, Endometriosis, Esophageal squamous cell carcinoma, Hypothyroidism, Lipidoses, Lipoidosis, Metabolic syndrome, Diabetes mellitus, type 2

504
TATA-box binding protein associated factor 6
ALYUS, MGC:8964, TAF(II)70, TAF(II)80, TAF2E, TAFII-70, TAFII-80, TAFII70, TAFII80, TAFII85
Alazami-yuan syndrome, Cornelia de lange syndrome, Global developmental delay

505
TATA-box binding protein associated factor 13
MRT60, TAF(II)18, TAF2K, TAFII-18, TAFII18
Primary microcephaly, Intellectual developmental disorder

506
TAL bHLH transcription factor 1, erythroid differentiation factor
SCL, TCL5, bHLHa17, tal-1
Insomnia, Acute lymphoblastic leukemia, Major depressive disorder, Metabolic syndrome, Neurotic disorder, Open angle glaucoma, Diabetes mellitus, type 2

507
TAL bHLH transcription factor 2
-
Acute lymphoblastic leukemia, Schizophrenia

508
Transaldolase 1
TAL, TAL-H, TALDOR, TALH
Carbohydrate metabolism disease, Hepatocellular carcinoma, Cataract, Kidney disease, Transaldolase deficiency, Parkinson disease

509
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, Glaucoma, Hypothyroidism, Myocardial ischemia, Prostatic neoplasm, Psoriasis, Rheumatoid arthritis, Rhinitis
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510
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, Gout, Hyperthyroidism, Hypothyroidism
View all (22 more)