SLC23A3 solute carrier family 23 member 3

Information
Symbol
SLC23A3
Type
protein-coding
Description
solute carrier family 23 member 3
Entrez Gene ID
151295
Genome
hg19
Position
chr2:220,026,488-220,034,754
Genome
hg38
Position
chr2:219,161,766-219,170,032
MIM
620339 OMIM
HGNC
HGNC:20601 HGNC
Ensembl
ENSG00000213901 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 2
Likely benign 0 4
Uncertain significance 0 28
Ranking
ClinVar
0
0
0
34
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 E2BP3
SYNONYM SVCT3
SYNONYM Yspl1
MIM 620339 OMIM
HGNC HGNC:20601 HGNC
Ensembl ENSG00000213901 Ensembl
AllianceGenome HGNC:20601
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000409878.8 hg38 chr2 219,161,465 219,170,029 8,565
ENST00000295738.11 hg38 chr2 219,161,465 219,170,095 8,631
ENST00000455516.6 hg38 chr2 219,161,766 219,170,032 8,267
ENST00000409878.8 hg19 chr2 220,026,187 220,034,751 8,565
ENST00000295738.11 hg19 chr2 220,026,187 220,034,817 8,631
ENST00000455516.6 hg19 chr2 220,026,488 220,034,754 8,267
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