DEDD2 death effector domain containing 2
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
not provided | 1 | 0 |
Uncertain significance | 0 | 36 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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36 |
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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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Search word | : | |
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 |
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SYNONYM | FLAME-3 |
SYNONYM | FLAME3 |
MIM | 617078 OMIM |
HGNC | HGNC:24450 HGNC |
Ensembl | ENSG00000160570 Ensembl |
AllianceGenome | HGNC:24450 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000336034.8 | hg38 | chr19 | 42,198,598 | 42,217,669 | 19,072 |
ENST00000598727.5 | hg38 | chr19 | 42,201,714 | 42,217,682 | 15,969 |
ENST00000596251.6 | hg38 | chr19 | 42,198,598 | 42,217,677 | 19,080 |
ENST00000595337.5 | hg38 | chr19 | 42,198,613 | 42,220,123 | 21,511 |
ENST00000336034.8 | hg19 | chr19 | 42,702,750 | 42,721,821 | 19,072 |
ENST00000596251.6 | hg19 | chr19 | 42,702,750 | 42,721,829 | 19,080 |
ENST00000595337.5 | hg19 | chr19 | 42,702,765 | 42,724,275 | 21,511 |
ENST00000598727.5 | hg19 | chr19 | 42,705,866 | 42,721,834 | 15,969 |
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