SLC35F1

solute carrier family 35 member F1
Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Amber SLC35F1 in Angelman Rett like syndromes


Level 2: Dysmorphic and congenital abnormality syndromes
Version 1.11

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • Neurodevelopmental disorder, MONDO:0700092, SLC35F1-associated
  • Rett-like syndrome

Amber SLC35F1 in Mendeliome


Version 1.2374

review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • Neruodevelopmental disorder, MONDO:0700092, SLC35F1-associated
  • Rett-like syndrome

Amber SLC35F1 in Intellectual disability syndromic and non-syndromic


Level 2: Neurology and neurodevelopmental disorders
Version 1.83

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • Neruodevelopmental disorder, MONDO:0700092, SLC35F1-associated
  • Rett-like syndrome