SLC25A15 solute carrier family 25 member 15

Information
Symbol
SLC25A15
Type
protein-coding
Description
solute carrier family 25 member 15
Entrez Gene ID
10166
Genome
hg19
Position
chr13:41,363,604-41,386,596
Genome
hg38
Position
chr13:40,789,468-40,812,460
MIM
603861 OMIM
HGNC
HGNC:10985 HGNC
Ensembl
ENSG00000102743 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 86
Likely pathogenic 0 76
Benign 0 82
Likely benign 0 370
Conflicting classifications of pathogenicity 0 30
not provided 0 4
Uncertain significance 0 244
Ranking
ClinVar
0
0
100
710
12
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 D13S327
SYNONYM HHH
SYNONYM LNC-HC
SYNONYM ORC1
SYNONYM ORNT1
MIM 603861 OMIM
HGNC HGNC:10985 HGNC
Ensembl ENSG00000102743 Ensembl
AllianceGenome HGNC:10985
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000338625.9 hg38 chr13 40,789,611 40,812,460 22,850
ENST00000707033.1 hg38 chr13 40,789,468 40,812,460 22,993
ENST00000707033.1 hg19 chr13 41,363,604 41,386,596 22,993
ENST00000338625.9 hg19 chr13 41,363,747 41,386,596 22,850
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