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 | |
---|---|
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0 |
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0 |
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0 |
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42 |
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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
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Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
Prediction | |||||
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
Search Word
Target data | : |
MGeND data only
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Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
Search Word
Target data | : |
MGeND data only
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Category | : |
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Filtering | : |
Name | MGeND | Type | Genome | Gene symbol | Chromosome | Genomic start | Genomic stop | Strand | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
Type | ID |
---|---|
SYNONYM | WHITE2 |
MIM | 607784 OMIM |
HGNC | HGNC:13884 HGNC |
Ensembl | ENSG00000172350 Ensembl |
AllianceGenome | HGNC:13884 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
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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