UBE2T

ubiquitin conjugating enzyme E2 T
OMIM: 610538, Gene2Phenotype

12 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 12 panels
Green UBE2T in Radial dysplasia Level 3: Dysmorphic disorders Level 2: Dysmorphic and congenital abnormality syndromes Version 1.25	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Other Eligibility statement prior genetic testing Phenotypes Fanconi Anemia, Complementation Group T, 616435
Green UBE2T in Haematological malignancies for rare disease Level 3: Tumour syndromes Level 2: Tumour syndromes Version 1.19	review	BIALLELIC, autosomal or pseudoautosomal	Sources Curated sources Expert Review Green Phenotypes Class: BM failure FA, (typ AR) Fanconi anemia MDS AML Squamous cell carcinoma: oral, GI, vulvar
Red UBE2T in Neurofibromatosis Type 1 Level 3: Muscle and nerve Level 2: Tumour syndromes Version 1.33	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red Literature Illumina TruGenome Clinical Sequencing Services Phenotypes Fanconi anaemia, complementation group T, 616435
Green UBE2T in COVID-19 research Level 2: Viral research Version 1.146	review	BIALLELIC, autosomal or pseudoautosomal	Sources IUIS Classification December 2019 Expert Review Green Phenotypes Fanconi anemia, complementation group T, 616435
Green UBE2T in Limb disorders Level 2: Musculoskeletal Version 7.17 Latest signed off version: v7.0 (30 Apr 2025) Component of the following Super Panels: Paediatric disorders	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Other Phenotypes Fanconi Anemia, Complementation Group T, 616435
Green UBE2T in Pigmentary skin disorders Level 2: Dermatology Version 4.13 Latest signed off version: v4.0 (30 Apr 2025)	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Expert Review Phenotypes FANCT FANCONI ANEMIA, COMPLEMENTATION GROUP T
Green UBE2T in Cytopenias and congenital anaemias Level 3: Anaemias and red cell disorders Level 2: Haematological disorders Version 1.123	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Radboud University Medical Center, Nijmegen BRIDGE consortium (NIHRBR-RD) Phenotypes Falcon anemia Fanconi anemia, complementation group T, 616435
Green UBE2T in Haematological malignancies cancer susceptibility Level 2: Cancer susceptibility Version 4.37 Latest signed off version: v4.0 (22 Mar 2023)	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Curated sources Phenotypes Class: BM failure FA, (typ AR) Fanconi anemia MDS AML Squamous cell carcinoma: oral, GI, vulvar
Green UBE2T in Confirmed Fanconi anaemia or Bloom syndrome Level 2: Haematology Version 2.13 Latest signed off version: v2.5 (1 May 2024)	review	BIALLELIC, autosomal or pseudoautosomal	Sources North West GLH Yorkshire and North East GLH NHS GMS Expert Review Green Wessex and West Midlands GLH Phenotypes 616435 Fanconi anemia, complementation group T Falcon anemia Fanconi anemia, complementation group T, 616435
Green UBE2T in Fetal anomalies Level 2: Fetal (including NIPD) Version 6.140 Latest signed off version: v6.0 (30 Apr 2025)	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green PAGE DD-Gene2Phenotype Phenotypes FANCONI ANEMIA, COMPLEMENTATION GROUP T
Green UBE2T in DDG2P Version 6.424 Latest signed off version: v6.0 (30 Apr 2025) Component of the following Super Panels: Paediatric disorders	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green DD-Gene2Phenotype Phenotypes FANCONI ANEMIA, COMPLEMENTATION GROUP T 616435
Green UBE2T in Monogenic short stature Level 2: Endocrinology Version 1.31 Latest signed off version: v1.0 (7 Aug 2024)	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Phenotypes Fanconi anemia, complementation group T, OMIM:616435