1. Genes and Genomic Entities
  2. SLC35F1

SLC35F1

solute carrier family 35 member F1
Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Red SLC35F1 in Intellectual disability


Level 2: Developmental disorders
Version 11.9
Latest signed off version: v11.0 (12 Aug 2026)

Component of the following Super Panels:

  • Hypotonic infant
  • Leukodystrophy, childhood onset
  • Paediatric disorders

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