CRADD CASP2 and RIPK1 domain containing adaptor with death domain
Information
- Symbol
- CRADD
- Type
- protein-coding
- Description
- CASP2 and RIPK1 domain containing adaptor with death domain
- Entrez Gene ID
- 8738
- Genome
- hg19
- Position
- chr12:94,071,493-94,244,532
- Genome
- hg38
- Position
- chr12:93,677,717-93,850,756
- MIM
- 603454 OMIM
- HGNC
- HGNC:2340 HGNC
- Ensembl
- ENSG00000169372 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 0 | 14 |
Likely pathogenic | 0 | 2 |
Benign | 0 | 20 |
Likely benign | 0 | 52 |
Conflicting classifications of pathogenicity | 0 | 2 |
Uncertain significance | 0 | 46 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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28 |
![]() |
94 |
![]() |
6 |
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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Category | : |
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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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Category | : |
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Search word | : | |
Filtering | : |
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
|
Category | : |
|
Search word | : | |
Filtering | : |
Name | MGeND | Type | Genome | Gene symbol | Chromosome | Genomic start | Genomic stop | Strand | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Entry | Origin | Type | Annotation |
Type | ID |
---|---|
SYNONYM | MRT34 |
SYNONYM | RAIDD |
MIM | 603454 OMIM |
HGNC | HGNC:2340 HGNC |
Ensembl | ENSG00000169372 Ensembl |
AllianceGenome | HGNC:2340 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000552033.5 | hg38 | chr12 | 93,677,377 | 93,738,625 | 61,249 |
ENST00000542893.2 | hg38 | chr12 | 93,677,717 | 93,850,756 | 173,040 |
ENST00000548483.5 | hg38 | chr12 | 93,677,399 | 93,894,727 | 217,329 |
ENST00000552983.5 | hg38 | chr12 | 93,677,375 | 93,738,636 | 61,262 |
ENST00000332896.8 | hg38 | chr12 | 93,677,375 | 93,850,756 | 173,382 |
ENST00000552983.5 | hg19 | chr12 | 94,071,151 | 94,132,412 | 61,262 |
ENST00000332896.8 | hg19 | chr12 | 94,071,151 | 94,244,532 | 173,382 |
ENST00000552033.5 | hg19 | chr12 | 94,071,153 | 94,132,401 | 61,249 |
ENST00000548483.5 | hg19 | chr12 | 94,071,175 | 94,288,503 | 217,329 |
ENST00000542893.2 | hg19 | chr12 | 94,071,493 | 94,244,532 | 173,040 |
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