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"
351 to 360 of 1188 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

351
THO complex subunit 7
NIF3L1BP1, fSAP24, hTREX30
Anorexia nervosa, Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Cataract, Major depressive disorder, Obsessive-compulsive disorder, Schizophrenia, Tourette syndrome, Diabetes mellitus type 2

352
Thrombopoietin
CAMT2, MGDF, MKCSF, ML, MPLLG, THC9, THCYT1, TPO
Amegakaryocytic thrombocytopenia, Aplastic anemia, Asthma, Cardiomyopathy, Congenital amegakaryocytic thrombocytopenia, Desbuquois syndrome, Thrombocytosis, Hemorrhagic disease, Thrombocythemia, Thrombocythemia with distal limb defects, Essential thrombocythemia, Thrombocytopenia

353
Thyroid hormone receptor alpha
AR7, CHNG6, EAR7, ERB-T-1, ERBA, ERBA1, NR1A1, THRA1, THRA2, THRalpha, THRalpha1, THRalpha2, TRalpha, TRalpha1, TRalpha2, c-ERBA-1, c-erbA
Asthma, Bipolar disorder, Obstructive pulmonary disease, Thyroid agenesis, Congenital thyroid atrophy, Congenital hypothyroidism, Congenital hypothyroidism without goiter, Endometriosis, Major depressive disorder, Neurodevelopmental disorder, Pancreatic cancer

354
Thyroid hormone receptor associated protein 3
BCLAF2, TRAP150
Atrial fibrillation, Gastroesophageal reflux disease, Diabetes mellitus type 2

355
Thyroid hormone receptor beta
C-ERBA-2, C-ERBA-BETA, ERBA2, GRTH, NR1A2, PRTH, THR1, THRB1, THRB2, THRbeta, THRbeta1, TRb, TRbeta, TRbeta1, Thrbeta2
Asthma, Atrial fibrillation, Atrial flutter, Attention deficit hyperactivity disorder, Autism, Clonal hematopoiesis, Colorectal cancer, Craniofacial abnormalities, Hearing loss, Macular dystrophy, Major depressive disorder, Metabolic syndrome, Neurodevelopmental disorder, Oligodendroglioma, Schizophrenia
View all (4 more)

356
Thyroid hormone responsive
LPGP1, Lpgp, S14, SPOT14, THRP
Carcinoma

357
Thrombospondin type 1 domain containing 1
ANIB12, LMPHM13, TMTSP, UNQ3010
Aneurysm, Aortic aneurysm, Vascular dementia, Cerebral saccular aneurysm, Non-immune hydrops fetalis, Intracranial aneurysm, Lymphatic malformation

358
Thrombospondin type 1 domain containing 4
AAT12, ADAMTSL-6, ADAMTSL6, FVSY9334, PRO34005
Alzheimer disease, Aortic aneurysm, Asthma, Autism, Bipolar disorder, Breast cancer, Obstructive pulmonary disease, Color vision deficiency, Colorectal cancer, Congenital contractural arachnodactyly, Coronary artery disease, Dental caries, Estrogen-receptor negative breast cancer, Thoracic aortic aneurysm and aortic dissection, Iga nephropathy
View all (9 more)

359
Thrombospondin type 1 domain containing 7A
-
Alzheimer disease, Angioedema, Anorexia nervosa, Anxiety disorder, Bipolar disorder, Cataract, Central nervous system cancer, Kidney disease, Colorectal cancer, Coronary artery disease, Crohn disease, Dementia, Bipolar depression, Dilated cardiomyopathy, Dry eye syndrome
View all (25 more)

360
Thrombospondin type 1 domain containing 7B
-
Astrocytoma, Attention deficit hyperactivity disorder, Bone neoplasms, Breast cancer, Central nervous system cancer, Connective tissue neoplasm, Corneal astigmatism, Dementia, Diverticular disease, Edema, Ehlers-danlos syndrome, Glioblastoma, Glioma, Insomnia, Interstitial lung disease
View all (15 more)