SLC9A5 solute carrier family 9 member A5

Information
Symbol
SLC9A5
Type
protein-coding
Description
solute carrier family 9 member A5
Entrez Gene ID
6553
Genome
hg19
Position
chr16:67,282,882-67,306,094
Genome
hg38
Position
chr16:67,248,979-67,272,191
MIM
600477 OMIM
HGNC
HGNC:11078 HGNC
Ensembl
ENSG00000135740 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 4
Uncertain significance 0 84
Ranking
ClinVar
0
0
0
88
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 NHE5
MIM 600477 OMIM
HGNC HGNC:11078 HGNC
Ensembl ENSG00000135740 Ensembl
AllianceGenome HGNC:11078
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000299798.16 hg38 chr16 67,248,979 67,272,191 23,213
ENST00000299798.16 hg19 chr16 67,282,882 67,306,094 23,213
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