ABCB9 ATP binding cassette subfamily B member 9

Information
Symbol
ABCB9
Type
protein-coding
Description
ATP binding cassette subfamily B member 9
Entrez Gene ID
23457
Genome
hg19
Position
chr12:123,413,547-123,466,196
Genome
hg38
Position
chr12:122,929,000-122,981,649
MIM
605453 OMIM
HGNC
HGNC:50 HGNC
Ensembl
ENSG00000150967 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 16
Uncertain significance 0 200
Ranking
ClinVar
0
0
0
216
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 EST122234
SYNONYM TAPL
MIM 605453 OMIM
HGNC HGNC:50 HGNC
Ensembl ENSG00000150967 Ensembl
AllianceGenome HGNC:50
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000542678.5 hg38 chr12 122,929,000 122,981,649 52,650
ENST00000344275.11 hg38 chr12 122,920,951 122,966,460 45,510
ENST00000346530.9 hg38 chr12 122,928,994 122,966,509 37,516
ENST00000442833.6 hg38 chr12 122,924,525 122,966,460 41,936
ENST00000280560.13 hg38 chr12 122,928,992 122,966,463 37,472
ENST00000540285.5 hg38 chr12 122,928,994 122,966,500 37,507
ENST00000392439.7 hg38 chr12 122,928,999 122,975,205 46,207
ENST00000344275.11 hg19 chr12 123,405,498 123,451,007 45,510
ENST00000442833.6 hg19 chr12 123,409,072 123,451,007 41,936
ENST00000280560.13 hg19 chr12 123,413,539 123,451,010 37,472
ENST00000540285.5 hg19 chr12 123,413,541 123,451,047 37,507
ENST00000346530.9 hg19 chr12 123,413,541 123,451,056 37,516
ENST00000392439.7 hg19 chr12 123,413,546 123,459,752 46,207
ENST00000542678.5 hg19 chr12 123,413,547 123,466,196 52,650
Genome browser