SLC39A2 solute carrier family 39 member 2

Information
Symbol
SLC39A2
Type
protein-coding
Description
solute carrier family 39 member 2
Entrez Gene ID
29986
Genome
hg19
Position
chr14:21,467,452-21,470,030
Genome
hg38
Position
chr14:20,999,293-21,001,871
MIM
612166 OMIM
HGNC
HGNC:17127 HGNC
Ensembl
ENSG00000165794 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 6
Likely benign 0 2
Uncertain significance 0 28
Ranking
ClinVar
0
0
0
36
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 6A1
SYNONYM ETI-1
SYNONYM ZIP-2
SYNONYM ZIP2
MIM 612166 OMIM
HGNC HGNC:17127 HGNC
Ensembl ENSG00000165794 Ensembl
AllianceGenome HGNC:17127
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000554422.5 hg38 chr14 20,999,255 21,001,721 2,467
ENST00000298681.5 hg38 chr14 20,999,293 21,001,871 2,579
ENST00000554422.5 hg19 chr14 21,467,414 21,469,880 2,467
ENST00000298681.5 hg19 chr14 21,467,452 21,470,030 2,579
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