SLC25A17 solute carrier family 25 member 17

Information
Symbol
SLC25A17
Type
protein-coding
Description
solute carrier family 25 member 17
Entrez Gene ID
10478
Genome
hg19
Position
chr22:41,165,634-41,215,350
Genome
hg38
Position
chr22:40,769,630-40,819,346
MIM
606795 OMIM
HGNC
HGNC:10987 HGNC
Ensembl
ENSG00000100372 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 4
Uncertain significance 0 36
Ranking
ClinVar
0
0
0
40
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 :
Search word :
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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 PMP34
MIM 606795 OMIM
HGNC HGNC:10987 HGNC
Ensembl ENSG00000100372 Ensembl
AllianceGenome HGNC:10987
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000544408.5 hg38 chr22 40,769,630 40,819,399 49,770
ENST00000435456.7 hg38 chr22 40,769,630 40,819,346 49,717
ENST00000435456.7 hg19 chr22 41,165,634 41,215,350 49,717
ENST00000544408.5 hg19 chr22 41,165,634 41,215,403 49,770
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