MAP3K2-DT MAP3K2 divergent transcript

Information
Symbol
MAP3K2-DT
Type
ncRNA
Description
MAP3K2 divergent transcript
Entrez Gene ID
100506922
Genome
hg19
Position
chr2:128,145,760-128,158,156
Genome
hg38
Position
chr2:127,388,184-127,400,580
HGNC
HGNC:54088 HGNC
Ensembl
ENSG00000236682 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Ranking
ClinVar
0
0
0
0
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
HGNC HGNC:54088 HGNC
Ensembl ENSG00000236682 Ensembl
AllianceGenome HGNC:54088
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000685004.2 hg38 chr2 127,388,242 127,398,707 10,466
ENST00000433673.2 hg38 chr2 127,388,184 127,400,580 12,397
ENST00000688447.1 hg38 chr2 127,388,202 127,406,228 18,027
ENST00000685635.1 hg38 chr2 127,388,178 127,389,411 1,234
ENST00000685635.1 hg19 chr2 128,145,754 128,146,987 1,234
ENST00000433673.2 hg19 chr2 128,145,760 128,158,156 12,397
ENST00000688447.1 hg19 chr2 128,145,778 128,163,804 18,027
ENST00000685004.2 hg19 chr2 128,145,818 128,156,283 10,466
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