SLC30A10 solute carrier family 30 member 10

Information
Symbol
SLC30A10
Type
protein-coding
Description
solute carrier family 30 member 10
Entrez Gene ID
55532
Genome
hg19
Position
chr1:220,083,787-220,101,899
Genome
hg38
Position
chr1:219,910,445-219,928,557
MIM
611146 OMIM
HGNC
HGNC:25355 HGNC
Ensembl
ENSG00000196660 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 10
Likely pathogenic 0 2
Benign 0 74
Likely benign 0 164
Conflicting classifications of pathogenicity 0 16
not provided 1 16
Uncertain significance 0 232
Ranking
ClinVar
0
0
52
412
10
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
Locus Zoom
Variants
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
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 HMDPC
SYNONYM HMNDYT1
SYNONYM ZNT10
SYNONYM ZNT8
SYNONYM ZRC1
SYNONYM ZnT-10
MIM 611146 OMIM
HGNC HGNC:25355 HGNC
Ensembl ENSG00000196660 Ensembl
AllianceGenome HGNC:25355
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000696608.1 hg38 chr1 219,910,445 219,959,018 48,574
ENST00000366926.4 hg38 chr1 219,910,445 219,928,557 18,113
ENST00000366926.4 hg19 chr1 220,083,787 220,101,899 18,113
ENST00000696608.1 hg19 chr1 220,083,787 220,132,360 48,574
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