SLC39A5 solute carrier family 39 member 5

Information
Symbol
SLC39A5
Type
protein-coding
Description
solute carrier family 39 member 5
Entrez Gene ID
283375
Genome
hg19
Position
chr12:56,624,436-56,631,630
Genome
hg38
Position
chr12:56,230,652-56,237,846
MIM
608730 OMIM
HGNC
HGNC:20502 HGNC
Ensembl
ENSG00000139540 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 6
Likely pathogenic 0 2
Benign 0 20
Likely benign 0 28
Uncertain significance 0 94
Ranking
ClinVar
0
0
10
134
4
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 :
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 LZT-Hs7
SYNONYM MYP24
SYNONYM ZIP5
MIM 608730 OMIM
HGNC HGNC:20502 HGNC
Ensembl ENSG00000139540 Ensembl
AllianceGenome HGNC:20502
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000454355.7 hg38 chr12 56,230,051 56,237,846 7,796
ENST00000266980.8 hg38 chr12 56,230,652 56,237,846 7,195
ENST00000454355.7 hg19 chr12 56,623,835 56,631,630 7,796
ENST00000266980.8 hg19 chr12 56,624,436 56,631,630 7,195
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