NCR2 natural cytotoxicity triggering receptor 2

Information
Symbol
NCR2
Type
protein-coding
Description
natural cytotoxicity triggering receptor 2
Entrez Gene ID
9436
Genome
hg19
Position
chr6:41,303,346-41,318,627
Genome
hg38
Position
chr6:41,335,608-41,350,889
MIM
604531 OMIM
HGNC
HGNC:6732 HGNC
Ensembl
ENSG00000096264 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 6
Likely benign 0 4
Uncertain significance 0 34
Ranking
ClinVar
0
0
0
44
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
[No Data.]
Locus Zoom
Variants
Search Word
Target data :
MGeND data only
Category :
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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 CD336
SYNONYM LY95
SYNONYM NK-p44
SYNONYM NKP44
SYNONYM dJ149M18.1
MIM 604531 OMIM
HGNC HGNC:6732 HGNC
Ensembl ENSG00000096264 Ensembl
AllianceGenome HGNC:6732
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000373089.10 hg38 chr6 41,335,608 41,350,889 15,282
ENST00000373083.8 hg38 chr6 41,335,655 41,350,858 15,204
ENST00000373086.3 hg38 chr6 41,335,851 41,350,864 15,014
ENST00000373089.10 hg19 chr6 41,303,346 41,318,627 15,282
ENST00000373083.8 hg19 chr6 41,303,393 41,318,596 15,204
ENST00000373086.3 hg19 chr6 41,303,589 41,318,602 15,014
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