SLC9A7 solute carrier family 9 member A7

Information
Symbol
SLC9A7
Type
protein-coding
Description
solute carrier family 9 member A7
Entrez Gene ID
84679
Genome
hg19
Position
chrX:46,458,686-46,618,553
Genome
hg38
Position
chrX:46,599,251-46,759,118
MIM
300368 OMIM
HGNC
HGNC:17123 HGNC
Ensembl
ENSG00000065923 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely pathogenic 0 2
Benign 0 24
Likely benign 0 60
Conflicting classifications of pathogenicity 0 4
not provided 6 0
Uncertain significance 0 170
Ranking
ClinVar
0
0
22
232
2
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
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 MRX108
SYNONYM NHE-7
SYNONYM NHE7
SYNONYM SLC9A6
MIM 300368 OMIM
HGNC HGNC:17123 HGNC
Ensembl ENSG00000065923 Ensembl
AllianceGenome HGNC:17123
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000616978.5 hg38 chrX 46,599,251 46,759,118 159,868
ENST00000328306.4 hg38 chrX 46,605,318 46,759,055 153,738
ENST00000616978.5 hg19 chrX 46,458,686 46,618,553 159,868
ENST00000328306.4 hg19 chrX 46,464,753 46,618,490 153,738
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