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
0
0
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
Category :
Search word :
Filtering :
Variant name Gene AA change CDS Japanese
frequency
TogoVar MGeND Genome ClinVar CIViC evidence DisGeNET entry COSMIC
occurrence
Prediction
Entry Origin Type Annotation Entry Origin Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Size Chromosome Start Stop Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
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
TypeID
SYNONYM MRT34
SYNONYM RAIDD
MIM 603454 OMIM
HGNC HGNC:2340 HGNC
Ensembl ENSG00000169372 Ensembl
AllianceGenome HGNC:2340
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
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
Genome browser