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 1188 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

951
Tripartite motif containing 9
RNF91, SPRING
Alzheimer disease, Gastroesophageal reflux disease, Orofacial cleft, Psychotic disorders, Schizophrenia, Scoliosis

952
Tripartite motif family like 2
SPRYD6
Prostate cancer, Systemic lupus erythematosus

953
Trio Rho guanine nucleotide exchange factor
ARHGEF23, MEBAS, MRD44, MRD63, tgat
Anaphylaxis, Angioedema, Asthma, Color vision deficiency, Deafness, Developmental delay, Essential tremor, Gout, Intellectual developmental disorder, Myeloid leukemia, Liver neoplasms, Major depressive disorder, Neuroblastoma, Neurodevelopmental disorder, Neuropathy
View all (2 more)

954
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

955
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

956
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

957
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

958
Thyroid hormone receptor interactor 4
ASC-1, ASC1, HsT17391, MDCDC, SMABF1, ZC2HC5
Alzheimer disease, Centronuclear myopathy, Congenital muscular dystrophy, Pericarditis, Spinal muscular atrophy

959
Thyroid hormone receptor interactor 6
OIP-1, OIP1, TRIP-6, TRIP6i2, ZRP-1
Alzheimer disease, Gastroesophageal reflux disease

960
Triple QxxK/R motif containing
C8orf83, PRO0845, UPF0599
Attention deficit hyperactivity disorder