NKX6-2 NK6 homeobox 2

Information
Symbol
NKX6-2
Type
protein-coding
Description
NK6 homeobox 2
Entrez Gene ID
84504
Genome
hg19
Position
chr10:134,596,685-134,599,651
Genome
hg38
Position
chr10:132,783,181-132,786,147
MIM
605955 OMIM
HGNC
HGNC:19321 HGNC
Ensembl
ENSG00000148826 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 20
Likely pathogenic 0 16
Benign 0 12
Likely benign 0 80
Conflicting classifications of pathogenicity 0 2
Uncertain significance 0 148
Ranking
ClinVar
0
0
30
226
14
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 GTX
SYNONYM NKX6.2
SYNONYM NKX6B
SYNONYM SPAX8
MIM 605955 OMIM
HGNC HGNC:19321 HGNC
Ensembl ENSG00000148826 Ensembl
AllianceGenome HGNC:19321
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000368592.8 hg38 chr10 132,783,181 132,786,147 2,967
ENST00000368592.8 hg19 chr10 134,596,685 134,599,651 2,967
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