SLC30A6 solute carrier family 30 member 6

Information
Symbol
SLC30A6
Type
protein-coding
Description
solute carrier family 30 member 6
Entrez Gene ID
55676
Genome
hg19
Position
chr2:32,390,933-32,446,593
Genome
hg38
Position
chr2:32,165,864-32,221,524
MIM
611148 OMIM
HGNC
HGNC:19305 HGNC
Ensembl
ENSG00000152683 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 4
Uncertain significance 0 50
Ranking
ClinVar
0
0
0
54
0
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
[No Data.]
Locus Zoom
Variants
Search Word
Target data :
MGeND data only
Category :
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Variant name Gene AA change CDS Japanese
frequency
TogoVar MGeND Genome ClinVar CIViC evidence DisGeNET entry COSMIC
occurrence
Prediction
Entry Origin Type Annotation Entry Origin Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Size Chromosome Start Stop Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Gene symbol Chromosome Genomic start Genomic stop Strand Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
TypeID
SYNONYM MST103
SYNONYM MSTP103
SYNONYM ZNT6
MIM 611148 OMIM
HGNC HGNC:19305 HGNC
Ensembl ENSG00000152683 Ensembl
AllianceGenome HGNC:19305
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000282587.9 hg38 chr2 32,165,864 32,224,379 58,516
ENST00000357055.7 hg38 chr2 32,165,841 32,224,112 58,272
ENST00000435660.5 hg38 chr2 32,165,841 32,224,112 58,272
ENST00000406369.2 hg38 chr2 32,165,869 32,224,099 58,231
ENST00000379343.6 hg38 chr2 32,165,864 32,221,524 55,661
ENST00000357055.7 hg19 chr2 32,390,910 32,449,181 58,272
ENST00000435660.5 hg19 chr2 32,390,910 32,449,181 58,272
ENST00000379343.6 hg19 chr2 32,390,933 32,446,593 55,661
ENST00000282587.9 hg19 chr2 32,390,933 32,449,448 58,516
ENST00000406369.2 hg19 chr2 32,390,938 32,449,168 58,231
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