NRSN2 neurensin 2

Information
Symbol
NRSN2
Type
protein-coding
Description
neurensin 2
Entrez Gene ID
80023
Genome
hg19
Position
chr20:328,549-335,497
Genome
hg38
Position
chr20:347,905-354,853
MIM
610666 OMIM
HGNC
HGNC:16229 HGNC
Ensembl
ENSG00000125841 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 10
Likely benign 0 2
Uncertain significance 0 28
Ranking
ClinVar
0
0
0
40
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 C20orf98
SYNONYM dJ1103G7.6
MIM 610666 OMIM
HGNC HGNC:16229 HGNC
Ensembl ENSG00000125841 Ensembl
AllianceGenome HGNC:16229
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000492242.6 hg38 chr20 346,883 354,830 7,948
ENST00000608467.5 hg38 chr20 347,120 359,405 12,286
ENST00000714404.1 hg38 chr20 347,905 354,853 6,949
ENST00000608736.1 hg38 chr20 349,249 359,660 10,412
ENST00000470439.6 hg38 chr20 348,220 354,829 6,610
ENST00000714402.1 hg38 chr20 347,111 354,810 7,700
ENST00000714403.1 hg38 chr20 347,117 353,635 6,519
ENST00000714400.1 hg38 chr20 346,974 354,804 7,831
ENST00000714401.1 hg38 chr20 347,111 354,699 7,589
ENST00000382291.7 hg38 chr20 347,024 354,868 7,845
ENST00000382285.7 hg38 chr20 347,111 354,862 7,752
ENST00000492242.6 hg19 chr20 327,527 335,474 7,948
ENST00000714400.1 hg19 chr20 327,618 335,448 7,831
ENST00000382291.7 hg19 chr20 327,668 335,512 7,845
ENST00000714401.1 hg19 chr20 327,755 335,343 7,589
ENST00000714402.1 hg19 chr20 327,755 335,454 7,700
ENST00000382285.7 hg19 chr20 327,755 335,506 7,752
ENST00000714403.1 hg19 chr20 327,761 334,279 6,519
ENST00000608467.5 hg19 chr20 327,764 340,049 12,286
ENST00000714404.1 hg19 chr20 328,549 335,497 6,949
ENST00000470439.6 hg19 chr20 328,864 335,473 6,610
ENST00000608736.1 hg19 chr20 329,893 340,304 10,412
Genome browser