SLC39A13 solute carrier family 39 member 13

Information
Symbol
SLC39A13
Type
protein-coding
Description
solute carrier family 39 member 13
Entrez Gene ID
91252
Genome
hg19
Position
chr11:47,430,141-47,438,047
Genome
hg38
Position
chr11:47,408,590-47,416,496
MIM
608735 OMIM
HGNC
HGNC:20859 HGNC
Ensembl
ENSG00000165915 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 2
Likely pathogenic 0 2
Benign 0 46
Likely benign 0 312
Conflicting classifications of pathogenicity 0 40
Uncertain significance 0 216
Ranking
ClinVar
0
0
126
444
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 :
Search word :
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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 EDSSPD3
SYNONYM LZT-Hs9
SYNONYM SCDEDS
SYNONYM ZIP13
MIM 608735 OMIM
HGNC HGNC:20859 HGNC
Ensembl ENSG00000165915 Ensembl
AllianceGenome HGNC:20859
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000524928.1 hg38 chr11 47,410,085 47,416,494 6,410
ENST00000533076.5 hg38 chr11 47,407,132 47,416,495 9,364
ENST00000354884.8 hg38 chr11 47,408,631 47,416,496 7,866
ENST00000362021.9 hg38 chr11 47,408,590 47,416,496 7,907
ENST00000531974.5 hg38 chr11 47,408,584 47,412,393 3,810
ENST00000533076.5 hg19 chr11 47,428,683 47,438,046 9,364
ENST00000531974.5 hg19 chr11 47,430,135 47,433,944 3,810
ENST00000362021.9 hg19 chr11 47,430,141 47,438,047 7,907
ENST00000354884.8 hg19 chr11 47,430,182 47,438,047 7,866
ENST00000524928.1 hg19 chr11 47,431,636 47,438,045 6,410
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