Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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Showing genes starting with "T"
951 to 960 of 1185 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

951
TRIO and F-actin binding protein
DFNB28, HRIHFB2122, TAP68, TARA, dJ37E16.4
Atrial fibrillation, Attention deficit hyperactivity disorder, Autism, Isolated sensorineural deafness, Nonsyndromic hearing loss, Deafness, Glaucoma, Hearing impairment, Hearing loss, Hereditary hearing loss, Meniere disease, Nephrolithiasis, Open angle glaucoma, Osteoarthritis

952
Thyroid hormone receptor interactor 11
ACG1A, CEV14, GMAP-210, GMAP210, ODCD, ODCD1, TRIP-11, TRIP230
Achondrogenesis, Connective tissue disease, Desbuquois syndrome, Major depressive disorder, Spondylometaphyseal dysplasia

953
Thyroid hormone receptor interactor 12
MRD49, TRIP-12, TRIPC, ULF
Clark-baraitser syndrome, Color vision deficiency, Neurodevelopmental disorder, Intellectual developmental disorder, Metabolic syndrome, Non-specific syndromic intellectual disability, Diabetes mellitus type 2

954
Thyroid hormone receptor interactor 13
16E1BP, MVA3, OOMD9, OZEMA9
Aneuploidy, Hepatocellular carcinoma, Female infertility, Mosaic variegated aneuploidy, Oocyte maturation defect, Post-traumatic stress disorder, Squamous cell carcinoma, Wilms tumor

955
Thyroid hormone receptor interactor 4
ASC-1, ASC1, HsT17391, MDCDC, SMABF1, ZC2HC5
Alzheimer disease, Centronuclear myopathy, Congenital muscular dystrophy, Pericarditis, Spinal muscular atrophy

956
Thyroid hormone receptor interactor 6
OIP-1, OIP1, TRIP-6, TRIP6i2, ZRP-1
Alzheimer disease, Gastroesophageal reflux disease

957
Triple QxxK/R motif containing
C8orf83, PRO0845, UPF0599
Attention deficit hyperactivity disorder

958
TRNA isopentenyltransferase 1
COXPD35, GRO1, IPPT, IPT, IPTase, MOD5, hGRO1
Androgenetic alopecia, Combined oxidative phosphorylation deficiency, Developmental and epileptic encephalopathy, Major depressive disorder, Mitochondrial disease

959
TRNA methyltransferase O
C9orf156, HSPC219, NAP1
Alzheimer disease, Androgenetic alopecia, Differentiated thyroid carcinoma, Orofacial cleft, Thyroid carcinoma, Thyroid cancer

960
TRNA methyltransferase 1
MRT68, TRM1, hTRM1
Intellectual developmental disorder, Non-specific syndromic intellectual disability