SLC39A4, solute carrier family 39 member 4, 55630

N. diseases: 87; N. variants: 12
Disease: Acrodermatitis enteropathica ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs782110796
rs782110796
Entrez Id: 55630
Gene Symbol: SLC39A4
SLC39A4
CUI: C0221036
Disease:
Acrodermatitis enteropathica 		0.700 GeneticVariation UNIPROT Complete sequencing and characterization of 21,243 full-length human cDNAs. 14702039 2004
dbSNP: rs782110796
rs782110796
Entrez Id: 55630
Gene Symbol: SLC39A4
SLC39A4
CUI: C0221036
Disease:
Acrodermatitis enteropathica 		0.700 GeneticVariation UNIPROT Novel SLC39A4 mutations in acrodermatitis enteropathica. 12787121 2003
dbSNP: rs782110796
rs782110796
Entrez Id: 55630
Gene Symbol: SLC39A4
SLC39A4
CUI: C0221036
Disease:
Acrodermatitis enteropathica 		0.700 GeneticVariation UNIPROT A novel member of a zinc transporter family is defective in acrodermatitis enteropathica. 12032886 2002
dbSNP: rs782110796
rs782110796
Entrez Id: 55630
Gene Symbol: SLC39A4
SLC39A4
CUI: C0221036
Disease:
Acrodermatitis enteropathica 		0.700 GeneticVariation UNIPROT Identification of SLC39A4, a gene involved in acrodermatitis enteropathica. 12068297 2002