FSCN1

fascin actin-bundling protein 1
OMIM: 602689, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Red FSCN1 in Mendeliome


Version 1.3050

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • Neurodevelopmental disorder, MONDO:0700092, FSCN1-related

Red FSCN1 in Intellectual disability syndromic and non-syndromic


Level 2: Neurology and neurodevelopmental disorders
Version 1.288

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • Neurodevelopmental disorder, MONDO:0700092, FSCN1-related