Genomics England
GMS Panels
Panels
Genes and Entities

SLC39A4

solute carrier family 39 member 4
OMIM: 607059
PanelMode of inheritanceDetails
5 panels
Green
in Epidermolysis bullosa and congenital skin fragility
R-numbers: R164
Signed-off version 2.16
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Acrodermatitis enteropathica, OMIM:201100
Green
in Intestinal failure or congenital diarrhoea
R-numbers: R331
Signed-off version 3.17
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Acrodermatitis enteropathica, OMIM:201100
Green
in Likely inborn error of metabolism
Component of the following Super Panels:
  • - Hypotonic infant
  • - Leukodystrophy, childhood onset
  • - Paediatric disorders
  • - Unexplained death in infancy and sudden unexplained death in childhood
R-numbers: R98
Signed-off version 9.29
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Acrodermatitis enteropathica (Disorder of zinc metabolism), Acrodermatitis enteropathica 201100 (Disorder of zinc metabolism)
Green
in Primary immunodeficiency or monogenic inflammatory bowel disease
R-numbers: R15
Signed-off version 9.91
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Acrodermatitis enteropathica, OMIM:201100, Disorder of zinc metabolism
Green
in Rare genetic inflammatory skin disorders
R-numbers: R332
Signed-off version 4.25
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Acrodermatitis enteropathica, OMIM:201100