MMP28 matrix metallopeptidase 28
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 14 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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14 |
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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
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 |
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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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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 | EPILYSIN |
SYNONYM | MM28 |
SYNONYM | MMP-25 |
SYNONYM | MMP-28 |
SYNONYM | MMP25 |
MIM | 608417 OMIM |
HGNC | HGNC:14366 HGNC |
Ensembl | ENSG00000271447 Ensembl |
AllianceGenome | HGNC:14366 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000605424.6 | hg38 | chr17 | 35,765,865 | 35,795,641 | 29,777 |
ENST00000615136.4 | hg38 | chr17 | 35,766,340 | 35,795,624 | 29,285 |
ENST00000612672.1 | hg38 | chr17 | 35,778,505 | 35,795,707 | 17,203 |
ENST00000605424.6 | hg19 | chr17 | 34,092,884 | 34,122,645 | 29,762 |
ENST00000615136.4 | hg19 | chr17 | 34,093,359 | 34,122,628 | 29,270 |
ENST00000612672.1 | hg19 | chr17 | 34,105,509 | 34,122,711 | 17,203 |
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