SLC30A7 (solute carrier family 30 member 7)

2014-08-01  

Identity

HGNC
LOCATION
1p21.2
LOCUSID
ALIAS
ZNT7,ZnT-7,ZnTL2
FUSION GENES

Other Information

Locus ID:

NCBI: 148867
MIM: 611149
HGNC: 19306
Ensembl: ENSG00000162695

Variants:

dbSNP: 148867
ClinVar: 148867
TCGA: ENSG00000162695
COSMIC: SLC30A7

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000162695ENST00000357650Q8NEW0
ENSG00000162695ENST00000370111H0Y362
ENSG00000162695ENST00000370112Q8NEW0

Expression (GTEx)

0
5
10
15
20

Pathways

PathwaySourceExternal ID
Metabolism of proteinsREACTOMER-HSA-392499
Peptide hormone metabolismREACTOMER-HSA-2980736
Insulin processingREACTOMER-HSA-264876
Transmembrane transport of small moleculesREACTOMER-HSA-382551
SLC-mediated transmembrane transportREACTOMER-HSA-425407
Transport of glucose and other sugars, bile salts and organic acids, metal ions and amine compoundsREACTOMER-HSA-425366
Metal ion SLC transportersREACTOMER-HSA-425410
Zinc transportersREACTOMER-HSA-435354
Zinc efflux and compartmentalization by the SLC30 familyREACTOMER-HSA-435368

Protein levels (Protein atlas)

Not detected
Low
Medium
High

References

Pubmed IDYearTitleCitations
383936932024Investigation of cuproptosis regulator-mediated modification patterns and SLC30A7 function in GBM.0
383936932024Investigation of cuproptosis regulator-mediated modification patterns and SLC30A7 function in GBM.0
368216392023Identification of novel compound heterozygous variants in the SLC30A7 (ZNT7) gene in two French brothers with stunted growth, testicular hypoplasia and bone marrow failure.2
368216392023Identification of novel compound heterozygous variants in the SLC30A7 (ZNT7) gene in two French brothers with stunted growth, testicular hypoplasia and bone marrow failure.2
356072882022MiR-200c-3p regulates pyroptosis by targeting SLC30A7 in diabetic retinopathy.0
357514292022De novo heterozygous variants in SLC30A7 are a candidate cause for Joubert syndrome.2
356072882022MiR-200c-3p regulates pyroptosis by targeting SLC30A7 in diabetic retinopathy.0
357514292022De novo heterozygous variants in SLC30A7 are a candidate cause for Joubert syndrome.2
336495342021ZnT7 RNAi favors Raf(GOF)scrib(-/-)-induced tumor growth and invasion in Drosophila through JNK signaling pathway.7
336495342021ZnT7 RNAi favors Raf(GOF)scrib(-/-)-induced tumor growth and invasion in Drosophila through JNK signaling pathway.7
285583002017Urine cadmium levels and albuminuria in a general population from Spain: A gene-environment interaction analysis.22
285583002017Urine cadmium levels and albuminuria in a general population from Spain: A gene-environment interaction analysis.22
232750322013Zinc transporter 5 and zinc transporter 7 induced by high glucose protects peritoneal mesothelial cells from undergoing apoptosis.8
232750322013Zinc transporter 5 and zinc transporter 7 induced by high glucose protects peritoneal mesothelial cells from undergoing apoptosis.8
214621062010Gastrointestinal factors influencing zinc absorption and homeostasis.42

Citation

Dessen P

SLC30A7 (solute carrier family 30 member 7)

Atlas Genet Cytogenet Oncol Haematol. 2014-08-01

Online version: http://atlasgeneticsoncology.org/gene/54636/css/lib/gene-fusions-explorer/