TCF7L1

transcription factor 7 like 1
OMIM: 604652, ClinGen, DECIPHER

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Red TCF7L1 in Mendeliome


Version 1.2302

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
Phenotypes
  • Congenital hypopituitarism

Amber TCF7L1 in Pituitary hormone deficiency


Level 2: Endocrine disorders
Version 0.35

0 reviews MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Genomics England PanelApp
  • Expert Review Amber
Phenotypes
  • No OMIM number
  • pituitary hormone deficiency