Genomic Map
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Target Gene Details
Entrez Gene ID: | 2908 |
Gene Name: | nuclear receptor subfamily 3 group C member 1 |
Gene Aliases: |
GCCR, GCR, GCRST, GR, GRL |
Location: |
Chr.5:143277931-143435512 on Build GRCh38 |
Assay Gene Location: | Within Exon 14 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| NR3C1 | NM_000176.2 | 9 | 4598 | NP_000167.1 |
| NM_001018074.1 | 9 | 4428 | NP_001018084.1 | |
| NM_001018075.1 | 9 | 4331 | NP_001018085.1 | |
| NM_001018076.1 | 9 | 4224 | NP_001018086.1 | |
| NM_001018077.1 | 9 | 5100 | NP_001018087.1 | |
| NM_001020825.1 | NP_001018661.1 | |||
| NM_001024094.1 | 9 | 4601 | NP_001019265.1 | |
| NM_001204258.1 | 9 | 4598 | NP_001191187.1 | |
| NM_001204259.1 | 9 | 4598 | NP_001191188.1 | |
| NM_001204260.1 | 9 | 4598 | NP_001191189.1 | |
| NM_001204261.1 | 9 | 4598 | NP_001191190.1 | |
| NM_001204262.1 | 9 | 4598 | NP_001191191.1 | |
| NM_001204263.1 | 9 | 4598 | NP_001191192.1 | |
| NM_001204264.1 | 9 | 4598 | NP_001191193.1 | |
| XM_011537637.2 | 8 | 5033 | XP_011535939.1 | |
| XM_017009397.1 | 9 | 4224 | XP_016864886.1 | |
| XM_017009398.1 | 9 | 4523 | XP_016864887.1 | |
| AM183262.1 | 9 | 4041 | ||
| X03225.1 | 9 | 4238 | CAA26976.1 | |
| X03348.1 | CAA27054.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv5041 | Chr.5:143273624 - 143318331 on Build GRCh38 | Deletion |
 NR3C1
|
| esv33748 | Chr.5:143258702 - 143320030 on Build GRCh38 | Loss |
NR3C1
|
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Set Membership: |
Intragenic
Exonic
DGV Variation
|
Gene Ontology Categories:
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