SLC39A6 solute carrier family 39 member 6

Information
Symbol
SLC39A6
Type
protein-coding
Description
solute carrier family 39 member 6
Entrez Gene ID
25800
Genome
hg19
Position
chr18:33,688,494-33,709,303
Genome
hg38
Position
chr18:36,108,531-36,129,340
MIM
608731 OMIM
HGNC
HGNC:18607 HGNC
Ensembl
ENSG00000141424 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 4
Uncertain significance 0 74
Ranking
ClinVar
0
0
0
78
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 LIV-1
SYNONYM LIV1
SYNONYM ZIP6
MIM 608731 OMIM
HGNC HGNC:18607 HGNC
Ensembl ENSG00000141424 Ensembl
AllianceGenome HGNC:18607
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000269187.10 hg38 chr18 36,108,531 36,129,340 20,810
ENST00000590986.5 hg38 chr18 36,109,148 36,129,381 20,234
ENST00000440549.6 hg38 chr18 36,111,000 36,129,385 18,386
ENST00000269187.10 hg19 chr18 33,688,494 33,709,303 20,810
ENST00000590986.5 hg19 chr18 33,689,111 33,709,344 20,234
ENST00000440549.6 hg19 chr18 33,690,963 33,709,348 18,386
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