Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
All A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
13821 to 13830 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

13821
Tensin 2
C1-TEN, C1TEN, TENC1
Hypertension, Nephrotic syndrome, Preeclampsia

13822
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

13823
Tensin 4
CTEN, PP14434
Alzheimer disease, Pancreatic cancer

13824
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)

13825
Transducer of ERBB2, 1
APRO5, APRO6, PIG49, TOB, TROB, TROB1
Chloracne, Endometriosis

13826
Transducer of ERBB2, 2
APRO5, TOB4, TOBL, TROB2
Asthma, Vitiligo

13827
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

13828
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

13829
TOG array regulator of axonemal microtubules 2
FAM179A
Deafness, Eosinophilia, Major depressive disorder, Venous thromboembolism

13830
Toll interacting protein
IL-1RAcPIP
Obstructive airway disease, Idiopathic pulmonary fibrosis, Interstitial lung disease