MPEG1 macrophage expressed 1
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 0 | 4 |
Benign | 0 | 6 |
Likely benign | 0 | 14 |
Uncertain significance | 0 | 106 |
Ranking
ClinVar | |
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0 |
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0 |
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2 |
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120 |
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8 |
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
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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 |
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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 |
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MGeND data only
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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 |
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SYNONYM | IMD77 |
SYNONYM | MPG1 |
SYNONYM | MPS1 |
SYNONYM | Mpg-1 |
SYNONYM | P-2 |
MIM | 610390 OMIM |
HGNC | HGNC:29619 HGNC |
Ensembl | ENSG00000197629 Ensembl |
AllianceGenome | HGNC:29619 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000361050.4 | hg38 | chr11 | 59,208,510 | 59,212,927 | 4,418 |
ENST00000361050.4 | hg19 | chr11 | 58,975,983 | 58,980,400 | 4,418 |
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