MEA1 male-enhanced antigen 1
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 4 |
Likely benign | 0 | 24 |
Conflicting classifications of pathogenicity | 0 | 2 |
Uncertain significance | 0 | 54 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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6 |
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74 |
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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
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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 |
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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 |
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Target data | : |
MGeND data only
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Category | : |
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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 | HYS |
SYNONYM | MEA |
MIM | 143170 OMIM |
HGNC | HGNC:6986 HGNC |
Ensembl | ENSG00000124733 Ensembl |
AllianceGenome | HGNC:6986 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000643776.1 | hg38 | chr6 | 43,012,082 | 43,013,983 | 1,902 |
ENST00000645410.1 | hg38 | chr6 | 43,012,094 | 43,016,868 | 4,775 |
ENST00000645375.1 | hg38 | chr6 | 43,012,094 | 43,016,866 | 4,773 |
ENST00000642748.1 | hg38 | chr6 | 43,012,094 | 43,014,279 | 2,186 |
ENST00000244711.4 | hg38 | chr6 | 43,011,143 | 43,013,946 | 2,804 |
ENST00000642555.1 | hg38 | chr6 | 43,011,143 | 43,013,684 | 2,542 |
ENST00000642555.1 | hg19 | chr6 | 42,978,881 | 42,981,422 | 2,542 |
ENST00000244711.4 | hg19 | chr6 | 42,978,881 | 42,981,684 | 2,804 |
ENST00000643776.1 | hg19 | chr6 | 42,979,820 | 42,981,721 | 1,902 |
ENST00000642748.1 | hg19 | chr6 | 42,979,832 | 42,982,017 | 2,186 |
ENST00000645375.1 | hg19 | chr6 | 42,979,832 | 42,984,604 | 4,773 |
ENST00000645410.1 | hg19 | chr6 | 42,979,832 | 42,984,606 | 4,775 |
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