Genomics England
GMS Panels
Panels
Genes and Entities

SLC25A24

solute carrier family 25 member 24
OMIM: 608744
PanelMode of inheritanceDetails
3 panels
Green
in DDG2P
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 3.79
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Gorlin-Chaudhry-Moss syndrome (GCMS), Syndrome with Hypertrichosis, Progeroid Appearance, and Mitochondrial Dysfunction
Green
in Fetal anomalies
R-numbers: R21, R412
Signed-off version 3.122
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Fontaine progeroid syndrome, OMIM, 612289, Fontaine progeroid syndrome, MONDO:0012853
Green
in Rare syndromic craniosynostosis or isolated multisuture synostosis
R-numbers: R100
Signed-off version 4.177
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Fontaine progeroid syndrome, OMIM, 612289, Fontaine progeroid syndrome, MONDO:0012853