SLC9A4 solute carrier family 9 member A4

Information
Symbol
SLC9A4
Type
protein-coding
Description
solute carrier family 9 member A4
Entrez Gene ID
389015
Genome
hg19
Position
chr2:103,089,685-103,150,431
Genome
hg38
Position
chr2:102,473,226-102,533,972
MIM
600531 OMIM
HGNC
HGNC:11077 HGNC
Ensembl
ENSG00000180251 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 2
Likely benign 0 4
association 0 8
Uncertain significance 0 92
Ranking
ClinVar
0
0
0
98
8
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 NHE4
MIM 600531 OMIM
HGNC HGNC:11077 HGNC
Ensembl ENSG00000180251 Ensembl
AllianceGenome HGNC:11077
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000295269.5 hg38 chr2 102,473,226 102,533,972 60,747
ENST00000295269.5 hg19 chr2 103,089,685 103,150,431 60,747
Genome browser