SLC22A24 solute carrier family 22 member 24

Information
Symbol
SLC22A24
Type
protein-coding
Description
solute carrier family 22 member 24
Entrez Gene ID
283238
Genome
hg19
Position
chr11:62,847,412-62,911,693
Genome
hg38
Position
chr11:63,079,940-63,144,221
MIM
611698 OMIM
HGNC
HGNC:28542 HGNC
Ensembl
ENSG00000197658 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 6
Uncertain significance 0 90
Ranking
ClinVar
0
0
0
96
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 :
Filtering :
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 NET46
MIM 611698 OMIM
HGNC HGNC:28542 HGNC
Ensembl ENSG00000197658 Ensembl
AllianceGenome HGNC:28542
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000417740.5 hg38 chr11 63,079,940 63,144,221 64,282
ENST00000612278.4 hg38 chr11 63,079,940 63,144,221 64,282
ENST00000326192.5 hg38 chr11 63,118,521 63,144,221 25,701
ENST00000417740.5 hg19 chr11 62,847,412 62,911,693 64,282
ENST00000612278.4 hg19 chr11 62,847,412 62,911,693 64,282
ENST00000326192.5 hg19 chr11 62,885,993 62,911,693 25,701
Genome browser