NR4A3 nuclear receptor subfamily 4 group A member 3
Information
- Symbol
- NR4A3
- Type
- protein-coding
- Description
- nuclear receptor subfamily 4 group A member 3
- Entrez Gene ID
- 8013
- Genome
- hg19
- Position
- chr9:102,589,009-102,629,173
- Genome
- hg38
- Position
- chr9:99,826,727-99,866,891
- MIM
- 600542 OMIM
- HGNC
- HGNC:7982 HGNC
- Ensembl
- ENSG00000119508 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely benign | 0 | 6 |
| not provided | 1 | 0 |
| Uncertain significance | 0 | 28 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
34 |
 |
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
Locus Zoom
Variants
Search Word
| Target data | : |
MGeND data only
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| 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
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| 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
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| Category | : |
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| 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 | CHN |
| SYNONYM | CSMF |
| SYNONYM | MINOR |
| SYNONYM | NOR1 |
| MIM | 600542 OMIM |
| HGNC | HGNC:7982 HGNC |
| Ensembl | ENSG00000119508 Ensembl |
| AllianceGenome | HGNC:7982 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000395097.7 | hg38 | chr9 | 99,821,885 | 99,866,891 | 45,007 |
| ENST00000330847.1 | hg38 | chr9 | 99,826,727 | 99,866,891 | 40,165 |
| ENST00000338488.8 | hg38 | chr9 | 99,821,855 | 99,834,059 | 12,205 |
| ENST00000618101.4 | hg38 | chr9 | 99,821,855 | 99,866,891 | 45,037 |
| ENST00000338488.8 | hg19 | chr9 | 102,584,137 | 102,596,341 | 12,205 |
| ENST00000618101.4 | hg19 | chr9 | 102,584,137 | 102,629,173 | 45,037 |
| ENST00000395097.7 | hg19 | chr9 | 102,584,167 | 102,629,173 | 45,007 |
| ENST00000330847.1 | hg19 | chr9 | 102,589,009 | 102,629,173 | 40,165 |
| Key | Value |
|---|---|
| strand | + |
| UniProt | OG |
| start | 102,584,136 |
| Gene Symbol | NR4A3 |
| Entrez GeneId | 8,013 |
| Chr Band | 9q22 |
| end | 102,629,172 |
| chr | chr9 |
| Name | nuclear receptor subfamily 4, group A, member 3 (NOR1) |
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