NR4A1 nuclear receptor subfamily 4 group A member 1
Information
- Symbol
- NR4A1
- Type
- protein-coding
- Description
- nuclear receptor subfamily 4 group A member 1
- Entrez Gene ID
- 3164
- Genome
- hg19
- Position
- chr12:52,431,499-52,453,285
- Genome
- hg38
- Position
- chr12:52,037,715-52,059,501
- MIM
- 139139 OMIM
- HGNC
- HGNC:7980 HGNC
- Ensembl
- ENSG00000123358 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 10 |
Likely benign | 0 | 10 |
Uncertain significance | 0 | 40 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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60 |
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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
[No Data.]
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 | |||||
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
Search Word
Target data | : |
MGeND data only
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Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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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 | GFRP1 |
SYNONYM | HMR |
SYNONYM | N10 |
SYNONYM | NAK-1 |
SYNONYM | NGFIB |
SYNONYM | NP10 |
SYNONYM | NUR77 |
SYNONYM | TR3 |
MIM | 139139 OMIM |
HGNC | HGNC:7980 HGNC |
Ensembl | ENSG00000123358 Ensembl |
AllianceGenome | HGNC:7980 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000394825.6 | hg38 | chr12 | 52,051,442 | 52,059,503 | 8,062 |
ENST00000550082.5 | hg38 | chr12 | 52,041,805 | 52,059,049 | 17,245 |
ENST00000394824.2 | hg38 | chr12 | 52,051,442 | 52,059,507 | 8,066 |
ENST00000243050.5 | hg38 | chr12 | 52,051,402 | 52,059,506 | 8,105 |
ENST00000360284.7 | hg38 | chr12 | 52,022,832 | 52,059,506 | 36,675 |
ENST00000545748.5 | hg38 | chr12 | 52,037,715 | 52,059,501 | 21,787 |
ENST00000548232.1 | hg38 | chr12 | 52,051,448 | 52,055,306 | 3,859 |
ENST00000360284.7 | hg19 | chr12 | 52,416,616 | 52,453,290 | 36,675 |
ENST00000394825.6 | hg19 | chr12 | 52,445,226 | 52,453,287 | 8,062 |
ENST00000394824.2 | hg19 | chr12 | 52,445,226 | 52,453,291 | 8,066 |
ENST00000243050.5 | hg19 | chr12 | 52,445,186 | 52,453,290 | 8,105 |
ENST00000545748.5 | hg19 | chr12 | 52,431,499 | 52,453,285 | 21,787 |
ENST00000550082.5 | hg19 | chr12 | 52,435,589 | 52,452,833 | 17,245 |
ENST00000548232.1 | hg19 | chr12 | 52,445,232 | 52,449,090 | 3,859 |
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