Phenotype: Acrodermatitis enteropathica


OMIM: 201100
Inheritance: Autosomal recessive
Classification: Endocrine, nutritional and metabolic disease

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SLC39A4 || c.1223_1227delCCGGG

Gene/Locus:    SLC39A4
Dna Change:    c.1223_1227delCCGGG
Protein Change:    p.Trp411ArgfsX7
Mutation Type:    Deletion
Mutation Effect:    Frameshift
Location:    exon 7
Transcript:    NM_130849.2

PopulationEthnic GroupRegionMutation FrquencyCoalescence TimeReference
TunisiaNANA6 unrelated familiesNASchmitt S et al., 2009Schmitt S, Küry S, Giraud M, Dréno B, Kharfi M, Bézieau S, . An update on mutations of the SLC39A4 gene in acrodermatitis enteropathica.. Hum. Mutat.. 2009; 30(6):926-33

SLC39A4 || c.143T>G

Gene/Locus:    SLC39A4
Dna Change:    c.143T>G
Protein Change:    p.Leu48X
Mutation Type:    Substitution
Mutation Effect:    Nonsense
Location:    exon 1
Transcript:    NM_130849.2

PopulationEthnic GroupRegionMutation FrquencyCoalescence TimeReference
TunisiaNANA3 unrelated familiesNASchmitt S et al., 2009Schmitt S, Küry S, Giraud M, Dréno B, Kharfi M, Bézieau S, . An update on mutations of the SLC39A4 gene in acrodermatitis enteropathica.. Hum. Mutat.. 2009; 30(6):926-33
TunisiaNANA3 patients/ 3 familiesNAKüry S et al., 2003Küry S, Kharfi M, Kamoun R, Taïeb A, Mallet E, Baudon JJ, Glastre C, Michel B, Sebag F, Brooks D, Schuster V, Scoul C, Dréno B, Bézieau S, Moisan JP, . Mutation spectrum of human SLC39A4 in a panel of patients with acrodermatitis enteropathica.. Hum. Mutat.. 2003; 22(4):337-8

References

Küry S, Kharfi M, Kamoun R, Taïeb A, Mallet E, Baudon JJ, Glastre C, Michel B, Sebag F, Brooks D, Schuster V, Scoul C, Dréno B, Bézieau S, Moisan JP, Mutation spectrum of human SLC39A4 in a panel of patients with acrodermatitis enteropathica.Hum. Mutat.. 2003; 22(4):337-8

Schmitt S, Küry S, Giraud M, Dréno B, Kharfi M, Bézieau S, An update on mutations of the SLC39A4 gene in acrodermatitis enteropathica.Hum. Mutat.. 2009; 30(6):926-33