SLC44A2 solute carrier family 44 member 2 (CTL2 blood group)

Information
Symbol
SLC44A2
Type
protein-coding
Description
solute carrier family 44 member 2 (CTL2 blood group)
Entrez Gene ID
57153
Genome
hg19
Position
chr19:10,736,201-10,755,233
Genome
hg38
Position
chr19:10,625,525-10,644,557
MIM
606106 OMIM
HGNC
HGNC:17292 HGNC
Ensembl
ENSG00000129353 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 4
Likely benign 0 10
Uncertain significance 0 70
Ranking
ClinVar
0
0
0
84
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 CTL2
SYNONYM PP1292
MIM 606106 OMIM
HGNC HGNC:17292 HGNC
Ensembl ENSG00000129353 Ensembl
AllianceGenome HGNC:17292
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000586078.5 hg38 chr19 10,625,525 10,644,557 19,033
ENST00000407327.8 hg38 chr19 10,602,510 10,644,550 42,041
ENST00000335757.10 hg38 chr19 10,625,553 10,644,557 19,005
ENST00000407327.8 hg19 chr19 10,713,186 10,755,226 42,041
ENST00000586078.5 hg19 chr19 10,736,201 10,755,233 19,033
ENST00000335757.10 hg19 chr19 10,736,229 10,755,233 19,005
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