RIPK4 receptor interacting serine/threonine kinase 4

Information
Symbol
RIPK4
Type
protein-coding
Description
receptor interacting serine/threonine kinase 4
Entrez Gene ID
54101
Genome
hg19
Position
chr21:43,159,533-43,187,212
Genome
hg38
Position
chr21:41,739,373-41,767,052
MIM
605706 OMIM
HGNC
HGNC:496 HGNC
Ensembl
ENSG00000183421 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 12
Likely pathogenic 0 4
Benign 0 116
Likely benign 0 138
Conflicting classifications of pathogenicity 0 20
Uncertain significance 0 248
Ranking
ClinVar
0
0
94
370
16
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 :
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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 ANKK2
SYNONYM ANKRD3
SYNONYM CHANDS
SYNONYM DIK
SYNONYM NKRD3
SYNONYM PKK
SYNONYM PPS2
SYNONYM RIP4
MIM 605706 OMIM
HGNC HGNC:496 HGNC
Ensembl ENSG00000183421 Ensembl
AllianceGenome HGNC:496
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000352483.3 hg38 chr21 41,739,369 41,767,089 27,721
ENST00000332512.8 hg38 chr21 41,739,373 41,767,052 27,680
ENST00000352483.3 hg19 chr21 43,159,529 43,187,249 27,721
ENST00000332512.8 hg19 chr21 43,159,533 43,187,212 27,680
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