SLC9B1 solute carrier family 9 member B1

Information
Symbol
SLC9B1
Type
protein-coding
Description
solute carrier family 9 member B1
Entrez Gene ID
150159
Genome
hg19
Position
chr4:103,822,085-103,940,862
Genome
hg38
Position
chr4:102,900,928-103,019,705
MIM
611527 OMIM
HGNC
HGNC:24244 HGNC
Ensembl
ENSG00000164037 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 2
Benign 0 6
Likely benign 0 50
not provided 226 0
Uncertain significance 0 68
Ranking
ClinVar
0
0
10
108
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
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 NHA1
SYNONYM NHEDC1
MIM 611527 OMIM
HGNC HGNC:24244 HGNC
Ensembl ENSG00000164037 Ensembl
AllianceGenome HGNC:24244
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000296422.12 hg38 chr4 102,900,928 103,019,705 118,778
ENST00000394789.7 hg38 chr4 102,885,048 103,019,719 134,672
ENST00000394789.7 hg19 chr4 103,806,205 103,940,876 134,672
ENST00000296422.12 hg19 chr4 103,822,085 103,940,862 118,778
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