NR4A2 nuclear receptor subfamily 4 group A member 2

Information
Symbol
NR4A2
Type
protein-coding
Description
nuclear receptor subfamily 4 group A member 2
Entrez Gene ID
4929
Genome
hg19
Position
chr2:157,180,949-157,189,233
Genome
hg38
Position
chr2:156,324,437-156,332,721
MIM
601828 OMIM
HGNC
HGNC:7981 HGNC
Ensembl
ENSG00000153234 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 16
Likely pathogenic 0 30
Benign 0 14
Likely benign 0 34
Conflicting classifications of pathogenicity 0 8
not provided 0 2
Uncertain significance 0 148
Ranking
ClinVar
0
0
4
220
16
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 HZF-3
SYNONYM IDLDP
SYNONYM NOT
SYNONYM NURR1
SYNONYM RNR1
SYNONYM TINUR
MIM 601828 OMIM
HGNC HGNC:7981 HGNC
Ensembl ENSG00000153234 Ensembl
AllianceGenome HGNC:7981
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000700228.1 hg38 chr2 156,324,908 156,332,762 7,855
ENST00000426264.5 hg38 chr2 156,325,082 156,332,714 7,633
ENST00000409108.6 hg38 chr2 156,325,744 156,330,707 4,964
ENST00000429376.5 hg38 chr2 156,325,744 156,330,721 4,978
ENST00000700231.1 hg38 chr2 156,325,352 156,332,684 7,333
ENST00000409572.5 hg38 chr2 156,325,098 156,342,348 17,251
ENST00000339562.9 hg38 chr2 156,324,437 156,332,721 8,285
ENST00000339562.9 hg19 chr2 157,180,949 157,189,233 8,285
ENST00000700228.1 hg19 chr2 157,181,420 157,189,274 7,855
ENST00000426264.5 hg19 chr2 157,181,594 157,189,226 7,633
ENST00000409572.5 hg19 chr2 157,181,610 157,198,860 17,251
ENST00000700231.1 hg19 chr2 157,181,864 157,189,196 7,333
ENST00000409108.6 hg19 chr2 157,182,256 157,187,219 4,964
ENST00000429376.5 hg19 chr2 157,182,256 157,187,233 4,978
Genome browser