NR1H3 nuclear receptor subfamily 1 group H member 3
Information
- Symbol
- NR1H3
- Type
- protein-coding
- Description
- nuclear receptor subfamily 1 group H member 3
- Entrez Gene ID
- 10062
- Genome
- hg19
- Position
- chr11:47,269,851-47,290,583
- Genome
- hg38
- Position
- chr11:47,248,300-47,269,032
- MIM
- 602423 OMIM
- HGNC
- HGNC:7966 HGNC
- Ensembl
- ENSG00000025434 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 0 | 2 |
Benign | 0 | 4 |
Likely benign | 0 | 8 |
Uncertain significance | 0 | 40 |
Ranking
ClinVar | |
---|---|
![]() |
0 |
![]() |
0 |
![]() |
0 |
![]() |
50 |
![]() |
4 |
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 |
Type | ID |
---|---|
SYNONYM | LXR-a |
SYNONYM | LXRA |
SYNONYM | RLD-1 |
MIM | 602423 OMIM |
HGNC | HGNC:7966 HGNC |
Ensembl | ENSG00000025434 Ensembl |
AllianceGenome | HGNC:7966 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000616973.4 | hg38 | chr11 | 47,248,300 | 47,269,032 | 20,733 |
ENST00000481889.6 | hg38 | chr11 | 47,248,924 | 47,268,831 | 19,908 |
ENST00000405853.7 | hg38 | chr11 | 47,257,998 | 47,268,843 | 10,846 |
ENST00000527949.1 | hg38 | chr11 | 47,260,397 | 47,268,817 | 8,421 |
ENST00000395397.7 | hg38 | chr11 | 47,248,916 | 47,268,812 | 19,897 |
ENST00000405576.5 | hg38 | chr11 | 47,248,916 | 47,268,843 | 19,928 |
ENST00000467728.5 | hg38 | chr11 | 47,257,979 | 47,268,845 | 10,867 |
ENST00000441012.7 | hg38 | chr11 | 47,257,996 | 47,269,033 | 11,038 |
ENST00000407404.5 | hg38 | chr11 | 47,248,956 | 47,268,781 | 19,826 |
ENST00000395397.7 | hg19 | chr11 | 47,270,467 | 47,290,363 | 19,897 |
ENST00000405576.5 | hg19 | chr11 | 47,270,467 | 47,290,394 | 19,928 |
ENST00000407404.5 | hg19 | chr11 | 47,270,507 | 47,290,332 | 19,826 |
ENST00000467728.5 | hg19 | chr11 | 47,279,530 | 47,290,396 | 10,867 |
ENST00000441012.7 | hg19 | chr11 | 47,279,547 | 47,290,584 | 11,038 |
ENST00000405853.7 | hg19 | chr11 | 47,279,549 | 47,290,394 | 10,846 |
ENST00000481889.6 | hg19 | chr11 | 47,270,475 | 47,290,382 | 19,908 |
ENST00000527949.1 | hg19 | chr11 | 47,281,948 | 47,290,368 | 8,421 |
ENST00000616973.4 | hg19 | chr11 | 47,269,851 | 47,290,583 | 20,733 |
Genome browser