SLC26A2 solute carrier family 26 member 2

Information
Symbol
SLC26A2
Type
protein-coding
Description
solute carrier family 26 member 2
Entrez Gene ID
1836
Genome
hg19
Position
chr5:149,340,321-149,366,963
Genome
hg38
Position
chr5:149,960,758-149,987,400
MIM
606718 OMIM
HGNC
HGNC:10994 HGNC
Ensembl
ENSG00000155850 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 4 230
Likely pathogenic 0 244
Benign 0 68
Likely benign 0 556
Conflicting classifications of pathogenicity 0 96
Uncertain significance 0 518
Ranking
ClinVar
0
0
246
1,182
38
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 D5S1708
SYNONYM DTD
SYNONYM DTDST
SYNONYM EDM4
SYNONYM MST153
SYNONYM MSTP157
MIM 606718 OMIM
HGNC HGNC:10994 HGNC
Ensembl ENSG00000155850 Ensembl
AllianceGenome HGNC:10994
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000286298.5 hg38 chr5 149,960,758 149,987,400 26,643
ENST00000286298.5 hg19 chr5 149,340,321 149,366,963 26,643
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