Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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13881 to 13890 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

13881
Tensin 1
MST091, MST122, MST127, MSTP091, MSTP122, MSTP127, MXRA6, PPP1R155, TNS
Asthma, Atrial fibrillation, Breast cancer, Obstructive pulmonary disease, Colorectal cancer, Coronary artery disease, Diverticular disease, Myocardial infarction, Open angle glaucoma, Psoriatic arthritis, Seasonal allergic rhinitis, Tetralogy of fallot, Diabetes mellitus type 2, Uterine fibroid

13882
Tensin 2
C1-TEN, C1TEN, TENC1
Hypertension, Nephrotic syndrome, Preeclampsia

13883
Tensin 3
TEM6, TENS1
Astrocytoma, Basal cell carcinoma, Behcet disease, Neoplasms, Colorectal cancer, Coronary artery disease, Dementia, Keratinocyte carcinoma, Non-small cell lung carcinoma, Oligodendroglioma, Orofacial cleft, Pancreatic cancer, Prostate cancer, Sarcoidosis, Scoliosis

13884
Tensin 4
CTEN, PP14434
Alzheimer disease, Pancreatic cancer

13885
Tenascin XB
EDS3, EDSCLL, EDSCLL1, HXBL, TENX, TN-X, TNX, TNXB1, TNXB2, TNXBS, VUR8, XB, XBS
Alzheimer disease, Eczema, Autism, Cervical cancer, Interstitial cystitis, Ehlers-danlos syndrome, Congenital adrenal hyperplasia, Coronary artery disease, Crohn disease, Dental caries, Diffuse gastric adenocarcinoma, Esophageal squamous cell carcinoma, Vesicoureteral reflux, Glaucoma, Hypertension
View all (20 more)

13886
Transducer of ERBB2, 1
APRO5, APRO6, PIG49, TOB, TROB, TROB1
Chloracne, Endometriosis

13887
Transducer of ERBB2, 2
APRO5, TOB4, TOBL, TROB2
Asthma, Vitiligo

13888
Target of EGR1, exonuclease
PCH7, TOE-1, hCaf1z
Congenital brain malformation, Congenital hypoplasia of part of brain, Congenital pontocerebellar hypoplasia, Hydranencephaly, Lissencephaly, Macrogyria, Microgyria, Pontocerebellar hypoplasia

13889
TOG array regulator of axonemal microtubules 1
FAM179B, JBTS37, KIAA0423
Brown tendon sheath syndrome, Ciliopathy, Congenital brain malformation, Congenital hypoplasia of part of brain, Aplasia of the vermis, Hydranencephaly, Joubert syndrome, Lissencephaly, Macrogyria, Microgyria

13890
TOG array regulator of axonemal microtubules 2
FAM179A
Deafness, Eosinophilia, Major depressive disorder, Venous thromboembolism