NINJ2-AS1 NINJ2 antisense RNA 1

Information
Symbol
NINJ2-AS1
Type
ncRNA
Description
NINJ2 antisense RNA 1
Entrez Gene ID
100049716
Genome
hg19
Position
chr12:740,057-755,044
Genome
hg38
Position
chr12:630,891-645,878
HGNC
HGNC:40405 HGNC
Ensembl
ENSG00000177406 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 :
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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:40405 HGNC
Ensembl ENSG00000177406 Ensembl
AllianceGenome HGNC:40405
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000537514.1 hg38 chr12 630,891 645,878 14,988
ENST00000662519.1 hg38 chr12 643,410 664,196 20,787
ENST00000666212.1 hg38 chr12 630,858 645,380 14,523
ENST00000666212.1 hg19 chr12 740,024 754,546 14,523
ENST00000537514.1 hg19 chr12 740,057 755,044 14,988
ENST00000662519.1 hg19 chr12 752,576 773,362 20,787
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