NR1D2 nuclear receptor subfamily 1 group D member 2

Information
Symbol
NR1D2
Type
protein-coding
Description
nuclear receptor subfamily 1 group D member 2
Entrez Gene ID
9975
Genome
hg19
Position
chr3:23,986,777-24,022,108
Genome
hg38
Position
chr3:23,945,286-23,980,617
MIM
602304 OMIM
HGNC
HGNC:7963 HGNC
Ensembl
ENSG00000174738 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely pathogenic 0 2
Benign 0 2
Likely benign 0 4
Uncertain significance 0 46
Ranking
ClinVar
0
0
0
52
2
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 BD73
SYNONYM EAR-1R
SYNONYM REVERBB
SYNONYM REVERBbeta
SYNONYM RVR
MIM 602304 OMIM
HGNC HGNC:7963 HGNC
Ensembl ENSG00000174738 Ensembl
AllianceGenome HGNC:7963
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000312521.9 hg38 chr3 23,945,286 23,980,617 35,332
ENST00000312521.9 hg19 chr3 23,986,777 24,022,108 35,332
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