Genesⓘ

Dataset:
? Reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "T"
441 to 450 of 913 Genes
Show
Entrez ID Gene Symbol Gene Name Synonyms Diseases

441
THO complex subunit 2
AMC7, CXorf3, MRX12, MRX35, THO2, XLID12, dJ506G2.1, hTREX120
Arthrogryposis multiplex congenita, Intellectual developmental disorder, x-linked, Intellectual developmental disorder, Neurodevelopmental disorders, X-linked intellectual disability

442
THAP domain containing 11
CTG-B43a, CTG-B45d, HRIHFB2206, MAHCL, RONIN, SCA51
Methylmalonic acidemia, Spinocerebellar ataxia

443
Tetratricopeptide repeat domain 7A
GIDID, MINAT, TTC7
Combined immunodeficiency, enteropathy spectrum, Combined immunodeficiency-multiple intestinal atresia, Common variable immunodeficiency, Erectile dysfunction, Gastrointestinal defects and immunodeficiency syndrome, Intestinal cancer, Lung cancer, Ovarian cancer, Ovarian serous carcinoma, Prostate cancer, Severe combined immunodeficiency, Squamous cell carcinoma

444
Tweety family member 1
-
Idiopathic pulmonary fibrosis

445
Teneurin transmembrane protein 2
ODZ2, TEN-M2, TEN2, TNM2, ten-2
Alzheimer disease, Anorexia nervosa, Astrocytoma, Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Breast cancer, Cancer, Cannabis abuse, Cardiovascular disease, Central nervous system cancer, Kidney disease, Colorectal cancer, Dementia, Diabetic neuropathy
View all (27 more)

446
TBC1 domain family member 24
DEE16, DFNA65, DFNB86, DOORS, EIEE16, EIM, EPRPDC, FIME, TLDC6
Auditory neuropathy, Isolated sensorineural deafness, Nonsyndromic hearing loss, Nonsyndromic intellectual disability, Cerebellar atrophy, Congenital neurologic anomalies , Deafness, Deafness with congenital onychodystrophy, Deafness, onychodystrophy, osteodystrophy, impaired intellectual development, and seizures syndrome, Developmental and epileptic encephalopathy, Doors syndrome, Dysarthria, Epilepsy of infancy with migrating focal seizures, Infantile myoclonic epilepsy, Rolandic epilepsy
View all (11 more)

447
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, Neurodevelopmental disorders, Non-specific syndromic intellectual disability

448
Twinfilin actin binding protein 1
A6, PTK9
Crohn disease, Inflammatory bowel disease, Lymphoma, Oligodendroglioma, Ulcerative colitis

449
TRNA methyltransferase 5
COXPD26, KIAA1393, PNSED, TRM5
Combined oxidative phosphorylation deficiency, Mitochondrial disease, Peripheral neuropathy with variable spasticity, exercise intolerance, and developmental delay

450
Transmembrane protein 181
GPR178, KIAA1423
Central nervous system cancer, Glaucoma, Glioblastoma, Glioma, Open angle glaucoma, Prostate cancer