SLC25A44 solute carrier family 25 member 44

Information
Symbol
SLC25A44
Type
protein-coding
Description
solute carrier family 25 member 44
Entrez Gene ID
9673
Genome
hg19
Position
chr1:156,163,723-156,182,586
Genome
hg38
Position
chr1:156,193,932-156,212,795
MIM
610824 OMIM
HGNC
HGNC:29036 HGNC
Ensembl
ENSG00000160785 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Uncertain significance 0 24
Ranking
ClinVar
0
0
0
24
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
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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
MIM 610824 OMIM
HGNC HGNC:29036 HGNC
Ensembl ENSG00000160785 Ensembl
AllianceGenome HGNC:29036
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000359511.5 hg38 chr1 156,194,104 156,212,796 18,693
ENST00000684582.1 hg38 chr1 156,194,103 156,211,446 17,344
ENST00000423538.6 hg38 chr1 156,193,932 156,212,795 18,864
ENST00000423538.6 hg19 chr1 156,163,723 156,182,586 18,864
ENST00000684582.1 hg19 chr1 156,163,894 156,181,237 17,344
ENST00000359511.5 hg19 chr1 156,163,895 156,182,587 18,693
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