Gene table of SLC39A4 : solute carrier family 39 member 4

Gene-disease associations table

Disease IDDisease nameSource of annotation with SLC39A4OMIM linkNumber of associated genesgenes
201100ACRODERMATITIS ENTEROPATHICA, ZINC-DEFICIENCY TYPEClinVar, OMIM, HUMSAVAR link to OMIM 1SLC39A4

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Annotation of the gene SLC39A4

Associated genes in ENSEMBL
Associated proteins - SwissProt Accession ID
Associated PDB IDs
Cytogenetic Band
Tandem repeats annotation
Transcription regulation as annotated in TRRUST
Associated KEGG pathways
KEGG pathwayKEGG IDKEGG IC
Mineral absorptionhsa049787.09
Associated REACTOME pathways
REACTOME pathwayREACTOME IDREACTOME IC
Transport of glucose and other sugars, bile salts and organic acids, metal ions and amine compoundsR-HSA-4253666.34
Transmembrane transport of small moleculesR-HSA-3825513.79
Zinc influx into cells by the SLC39 gene familyR-HSA-4423809.66
SLC-mediated transmembrane transportR-HSA-4254074.95
Zinc transportersR-HSA-4353548.89
Metal ion SLC transportersR-HSA-4254108.34
Associated GO terms for Molecular function
GO termGO IDGO IC
substrate-specific transmembrane transporter activityGO:00228912.9
inorganic cation transmembrane transporter activityGO:00228903.49
substrate-specific transporter activityGO:00228922.72
transition metal ion transmembrane transporter activityGO:00469156.05
transporter activityGO:00052152.57
cation transmembrane transporter activityGO:00083243.32
divalent inorganic cation transmembrane transporter activityGO:00725094.62
ion transmembrane transporter activityGO:00150753.04
transmembrane transporter activityGO:00228572.82
zinc ion transmembrane transporter activityGO:00053856.56
metal ion transmembrane transporter activityGO:00468733.71