T

T brachyury transcription factor
OMIM: 601397, Gene2Phenotype

6 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 6 panels
Red T in Currarino triad Version 1.1	review	BIALLELIC, autosomal or pseudoautosomal	Sources Radboud University Medical Center, Nijmegen Phenotypes Sacral agenesis with vertebral anomalies,615709 Tags new-gene-name
Red T in Familial Neural Tube Defects Version 1.10	review	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Sources Other Phenotypes Susceptibility to neural tube defects Tags new-gene-name
Red T in Childhood solid tumours Level 3: Childhood Tumours Level 2: Tumour syndromes Version 4.18 Latest signed off version: v4.0 (22 Mar 2023)	review	Not set	Sources Expert Review Red Expert List Tags new-gene-name
Green T in Sarcoma cancer susceptibility Level 3: Pertinent cancer susceptibility gene panel Level 2: Cancer Programme Version 1.25	review	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Sources Expert Review Green Expert list Phenotypes Chordoma (disease), MONDO:0008978 Tags new-gene-name cnv
Red T in Non-syndromic familial congenital anorectal malformations Level 3: Gastrointestinal disorders Level 2: Gastroenterological disorders Version 1.9	review	Not set	Sources Literature Phenotypes sacral agenesis anorectal atresia Tags new-gene-name
Green T in Sarcoma susceptibility Version 1.81 Latest signed off version: v1.2 (18 Feb 2020)	review	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Sources Expert Review Green NHS GMS Expert Review Green Expert list Phenotypes Chordoma (disease), MONDO:0008978 Tags new-gene-name