SLC25A37 solute carrier family 25 member 37

Information
Symbol
SLC25A37
Type
protein-coding
Description
solute carrier family 25 member 37
Entrez Gene ID
51312
Genome
hg19
Position
chr8:23,386,469-23,432,976
Genome
hg38
Position
chr8:23,528,956-23,575,463
MIM
610387 OMIM
HGNC
HGNC:29786 HGNC
Ensembl
ENSG00000147454 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 4
Likely benign 0 2
Uncertain significance 0 36
Ranking
ClinVar
0
0
0
42
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 HT015
SYNONYM MFRN
SYNONYM MFRN1
SYNONYM MSC
SYNONYM MSCP
SYNONYM PRO1278
SYNONYM PRO1584
SYNONYM PRO2217
MIM 610387 OMIM
HGNC HGNC:29786 HGNC
Ensembl ENSG00000147454 Ensembl
AllianceGenome HGNC:29786
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000519973.6 hg38 chr8 23,528,956 23,575,463 46,508
ENST00000519973.6 hg19 chr8 23,386,469 23,432,976 46,508
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