NR1H2 nuclear receptor subfamily 1 group H member 2

Information
Symbol
NR1H2
Type
protein-coding
Description
nuclear receptor subfamily 1 group H member 2
Entrez Gene ID
7376
Genome
hg19
Position
chr19:50,861,863-50,886,644
Genome
hg38
Position
chr19:50,358,606-50,383,387
MIM
600380 OMIM
HGNC
HGNC:7965 HGNC
Ensembl
ENSG00000131408 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 6
Uncertain significance 0 72
Ranking
ClinVar
0
0
0
76
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 LXR-b
SYNONYM LXRB
SYNONYM NER
SYNONYM NER-I
SYNONYM RIP15
SYNONYM UNR
MIM 600380 OMIM
HGNC HGNC:7965 HGNC
Ensembl ENSG00000131408 Ensembl
AllianceGenome HGNC:7965
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000652203.1 hg38 chr19 50,358,606 50,383,387 24,782
ENST00000593926.5 hg38 chr19 50,377,245 50,382,944 5,700
ENST00000598168.5 hg38 chr19 50,376,458 50,382,978 6,521
ENST00000411902.6 hg38 chr19 50,376,459 50,382,731 6,273
ENST00000253727.10 hg38 chr19 50,376,457 50,383,388 6,932
ENST00000599105.5 hg38 chr19 50,376,473 50,382,950 6,478
ENST00000652203.1 hg19 chr19 50,861,863 50,886,644 24,782
ENST00000253727.10 hg19 chr19 50,879,714 50,886,645 6,932
ENST00000598168.5 hg19 chr19 50,879,715 50,886,235 6,521
ENST00000411902.6 hg19 chr19 50,879,716 50,885,988 6,273
ENST00000599105.5 hg19 chr19 50,879,730 50,886,207 6,478
ENST00000593926.5 hg19 chr19 50,880,502 50,886,201 5,700
Genome browser