NME2 NME/NM23 nucleoside diphosphate kinase 2

Information
Symbol
NME2
Type
protein-coding
Description
NME/NM23 nucleoside diphosphate kinase 2
Entrez Gene ID
4831
Genome
hg19
Position
chr17:49,243,925-49,249,105
Genome
hg38
Position
chr17:51,166,564-51,171,744
MIM
156491 OMIM
HGNC
HGNC:7850 HGNC
Ensembl
ENSG00000243678 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
Ranking
ClinVar
0
0
0
2
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 NDKB
SYNONYM NDPK-B
SYNONYM NDPKB
SYNONYM NM23-H2
SYNONYM NM23B
SYNONYM PUF
MIM 156491 OMIM
HGNC HGNC:7850 HGNC
Ensembl ENSG00000243678 Ensembl
AllianceGenome HGNC:7850
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000513177.5 hg38 chr17 51,165,815 51,171,743 5,929
ENST00000393190.4 hg38 chr17 51,166,564 51,171,744 5,181
ENST00000393183.7 hg38 chr17 51,166,420 51,171,744 5,325
ENST00000512737.6 hg38 chr17 51,166,411 51,171,744 5,334
ENST00000514264.6 hg38 chr17 51,165,435 51,171,744 6,310
ENST00000503064.5 hg38 chr17 51,166,418 51,171,744 5,327
ENST00000514264.6 hg19 chr17 49,242,796 49,249,105 6,310
ENST00000513177.5 hg19 chr17 49,243,176 49,249,104 5,929
ENST00000512737.6 hg19 chr17 49,243,772 49,249,105 5,334
ENST00000503064.5 hg19 chr17 49,243,779 49,249,105 5,327
ENST00000393183.7 hg19 chr17 49,243,781 49,249,105 5,325
ENST00000393190.4 hg19 chr17 49,243,925 49,249,105 5,181
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