ADAM7 ADAM metallopeptidase domain 7
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 6 |
not provided | 1 | 0 |
Uncertain significance | 0 | 92 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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98 |
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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
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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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 | ADAM 7 |
SYNONYM | ADAM-7 |
SYNONYM | EAPI |
SYNONYM | GP-83 |
SYNONYM | GP83 |
MIM | 607310 OMIM |
HGNC | HGNC:214 HGNC |
Ensembl | ENSG00000069206 Ensembl |
AllianceGenome | HGNC:214 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000380789.5 | hg38 | chr8 | 24,441,084 | 24,509,548 | 68,465 |
ENST00000441335.6 | hg38 | chr8 | 24,440,930 | 24,467,647 | 26,718 |
ENST00000520720.1 | hg38 | chr8 | 24,475,904 | 24,526,970 | 51,067 |
ENST00000175238.10 | hg38 | chr8 | 24,441,026 | 24,509,565 | 68,540 |
ENST00000441335.6 | hg19 | chr8 | 24,298,443 | 24,325,160 | 26,718 |
ENST00000175238.10 | hg19 | chr8 | 24,298,539 | 24,367,078 | 68,540 |
ENST00000380789.5 | hg19 | chr8 | 24,298,597 | 24,367,061 | 68,465 |
ENST00000520720.1 | hg19 | chr8 | 24,333,417 | 24,384,483 | 51,067 |
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