SLC22A25 solute carrier family 22 member 25

Information
Symbol
SLC22A25
Type
protein-coding
Description
solute carrier family 22 member 25
Entrez Gene ID
387601
Genome
hg19
Position
chr11:62,925,909-63,011,071
Genome
hg38
Position
chr11:63,158,437-63,243,599
MIM
610792 OMIM
HGNC
HGNC:32935 HGNC
Ensembl
ENSG00000196600 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 2
Likely benign 0 26
Uncertain significance 0 62
Ranking
ClinVar
0
0
2
88
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 :
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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 :
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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 HIMTP
SYNONYM UST6
MIM 610792 OMIM
HGNC HGNC:32935 HGNC
Ensembl ENSG00000196600 Ensembl
AllianceGenome HGNC:32935
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000306494.11 hg38 chr11 63,158,437 63,243,599 85,163
ENST00000306494.11 hg19 chr11 62,925,909 63,011,071 85,163
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