PanelApp
  1. Genes and Genomic Entities
  2. SLC35C1

SLC35C1

solute carrier family 35 member C1
OMIM: 605881, Gene2Phenotype

8 panels

Panel Reviews Mode of inheritance Details
8 panels

Green SLC35C1 in Congenital Disorders of Glycosylation


Level 2: Metabolic disorders
Version 1.78

Component of the following Super Panels:

  • Metabolic Disorders Superpanel
  • Progressive Neurological Conditions

    		•  1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Victorian Clinical Genetics Services
    Phenotypes
    • Congenital disorder of glycosylation, type IIc, MIM# 266265, MONDO:0009953

    Green SLC35C1 in Mendeliome


    Version 1.3499

    		1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Victorian Clinical Genetics Services
    Phenotypes
    • Congenital disorder of glycosylation, type IIc, MIM# 266265, MONDO:0009953

    Green SLC35C1 in Phagocyte Defects


    Level 2: Immunological disorders
    Version 1.44

    Component of the following Super Panels:

  • Immunological disorders_SuperPanel

    		•  1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Melbourne Genomics Health Alliance Immunology Flagship
    • Victorian Clinical Genetics Services
    • Melbourne Genomics Health Alliance Immunology Flagship
    • Victorian Clinical Genetics Services
    Phenotypes
    • Congenital disorder of glycosylation, type IIc, MIM# 266265, MONDO:0009953

    Green SLC35C1 in Intellectual disability syndromic and non-syndromic


    Level 2: Neurology and neurodevelopmental disorders
    Version 1.398

    		1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Genetic Health Queensland
    Phenotypes
    • Congenital disorder of glycosylation, type IIc, MIM# 266265, MONDO:0009953

    Green SLC35C1 in Skeletal dysplasia

    Level 3: Skeletal dysplasias
    Level 2: Skeletal disorders
    Version 0.346

    		1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Expert Review Green
    • Other
    • Victorian Clinical Genetics Services
    Phenotypes
    • GDP-fucose transporter deficiency (Disorders of multiple glycosylation and other glycosylation pathways)
    • Congenital disorder of glycosylation, type IIc 266265

    Red SLC35C1 in Additional findings_Paediatric


    Level 2: Screening
    Version 0.278

    		0 reviews BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Red
    • BabySeq Category C gene
    Phenotypes
    • Congenital disorder of glycosylation 2c

    Amber SLC35C1 in Fetal anomalies


    Version 1.465

    		1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Amber
    • Genomics England PanelApp
    • Victorian Clinical Genetics Services
    Phenotypes
    • Congenital disorder of glycosylation, type IIc, MIM# 266265, MONDO:0009953

    Amber SLC35C1 in Genomic newborn screening: BabyScreen+


    Level 2: Screening
    Version 1.140

    		1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Amber
    • BabySeq Category C gene
    Phenotypes
    • Congenital disorder of glycosylation, type IIc, MIM# 266265, MONDO:0009953
    Tags
    • for review
    • metabolic