NKX2-2 NK2 homeobox 2

Information
Symbol
NKX2-2
Type
protein-coding
Description
NK2 homeobox 2
Entrez Gene ID
4821
Genome
hg19
Position
chr20:21,491,655-21,494,702
Genome
hg38
Position
chr20:21,511,017-21,514,064
MIM
604612 OMIM
HGNC
HGNC:7835 HGNC
Ensembl
ENSG00000125820 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely pathogenic 0 2
Benign 0 14
Likely benign 0 34
Conflicting classifications of pathogenicity 0 2
Uncertain significance 0 20
Ranking
ClinVar
0
0
8
60
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 :
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 NKX2.2
SYNONYM NKX2B
MIM 604612 OMIM
HGNC HGNC:7835 HGNC
Ensembl ENSG00000125820 Ensembl
AllianceGenome HGNC:7835
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000377142.5 hg38 chr20 21,511,017 21,514,064 3,048
ENST00000377142.5 hg19 chr20 21,491,655 21,494,702 3,048
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