SLC39A9 solute carrier family 39 member 9

Information
Symbol
SLC39A9
Type
protein-coding
Description
solute carrier family 39 member 9
Entrez Gene ID
55334
Genome
hg19
Position
chr14:69,865,409-69,929,107
Genome
hg38
Position
chr14:69,398,692-69,462,390
MIM
619116 OMIM
HGNC
HGNC:20182 HGNC
Ensembl
ENSG00000029364 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 2
Uncertain significance 0 8
Ranking
ClinVar
0
0
0
10
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 ZIP-9
SYNONYM ZIP9
MIM 619116 OMIM
HGNC HGNC:20182 HGNC
Ensembl ENSG00000029364 Ensembl
AllianceGenome HGNC:20182
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000336643.10 hg38 chr14 69,398,692 69,462,390 63,699
ENST00000557046.1 hg38 chr14 69,399,370 69,458,593 59,224
ENST00000556605.5 hg38 chr14 69,398,690 69,462,388 63,699
ENST00000031146.8 hg38 chr14 69,398,692 69,462,381 63,690
ENST00000556605.5 hg19 chr14 69,865,407 69,929,105 63,699
ENST00000031146.8 hg19 chr14 69,865,409 69,929,098 63,690
ENST00000336643.10 hg19 chr14 69,865,409 69,929,107 63,699
ENST00000557046.1 hg19 chr14 69,866,087 69,925,310 59,224
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