ABCG4 ATP binding cassette subfamily G member 4

Information
Symbol
ABCG4
Type
protein-coding
Description
ATP binding cassette subfamily G member 4
Entrez Gene ID
64137
Genome
hg19
Position
chr11:119,019,762-119,033,362
Genome
hg38
Position
chr11:119,149,052-119,162,653
MIM
607784 OMIM
HGNC
HGNC:13884 HGNC
Ensembl
ENSG00000172350 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 6
Likely benign 0 6
Uncertain significance 0 32
Ranking
ClinVar
0
0
0
42
2
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 WHITE2
MIM 607784 OMIM
HGNC HGNC:13884 HGNC
Ensembl ENSG00000172350 Ensembl
AllianceGenome HGNC:13884
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000622721.1 hg38 chr11 119,149,896 119,161,648 11,753
ENST00000615496.4 hg38 chr11 119,149,513 119,161,436 11,924
ENST00000619701.5 hg38 chr11 119,149,052 119,162,653 13,602
ENST00000619701.5 hg19 chr11 119,019,762 119,033,362 13,601
ENST00000615496.4 hg19 chr11 119,020,223 119,032,145 11,923
ENST00000622721.1 hg19 chr11 119,020,606 119,032,357 11,752
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