MDK midkine

Information
Symbol
MDK
Type
protein-coding
Description
midkine
Entrez Gene ID
4192
Genome
hg19
Position
chr11:46,402,306-46,405,349
Genome
hg38
Position
chr11:46,380,756-46,383,799
MIM
162096 OMIM
HGNC
HGNC:6972 HGNC
Ensembl
ENSG00000110492 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Uncertain significance 0 10
Ranking
ClinVar
0
0
0
10
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 ARAP
SYNONYM MK
SYNONYM NEGF2
MIM 162096 OMIM
HGNC HGNC:6972 HGNC
Ensembl ENSG00000110492 Ensembl
AllianceGenome HGNC:6972
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000407067.1 hg38 chr11 46,381,753 46,383,783 2,031
ENST00000395569.8 hg38 chr11 46,381,669 46,383,825 2,157
ENST00000395565.5 hg38 chr11 46,381,711 46,383,837 2,127
ENST00000395566.9 hg38 chr11 46,381,669 46,383,801 2,133
ENST00000359803.7 hg38 chr11 46,381,068 46,383,825 2,758
ENST00000405308.6 hg38 chr11 46,380,756 46,383,799 3,044
ENST00000405308.6 hg19 chr11 46,402,306 46,405,349 3,044
ENST00000359803.7 hg19 chr11 46,402,618 46,405,375 2,758
ENST00000395566.9 hg19 chr11 46,403,219 46,405,351 2,133
ENST00000395569.8 hg19 chr11 46,403,219 46,405,375 2,157
ENST00000395565.5 hg19 chr11 46,403,261 46,405,387 2,127
ENST00000407067.1 hg19 chr11 46,403,303 46,405,333 2,031
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