Genomic Map
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Target Gene Details
Entrez Gene ID: | 3977 |
Gene Name: | leukemia inhibitory factor receptor alpha |
Gene Aliases: |
CD118, LIF-R, SJS2, STWS, SWS |
Location: |
Chr.5:38474963-38606290 on Build GRCh38 |
Assay Gene Location: | Within Exon 25 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| LIFR | NM_001127671.1 | 20 | 9952 | NP_001121143.1 |
| NM_002310.5 | 20 | 9784 | NP_002301.1 | |
| XM_017009462.1 | 20 | 9797 | XP_016864951.1 | |
| BQ008945.1 | 1 | 324 | ||
| BX648635.1 | 1 | 4177 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| esv3604768 | Chr.5:38395532 - 38507296 on Build GRCh38 | Gain |
 LIFR
EGFLAM
EGFLAM-AS2
|
| esv3604761 | Chr.5:38056637 - 38805862 on Build GRCh38 | Gain |
OSMR-AS1
MIR3650
EGFLAM-AS4
LIFR
LINC01265
EGFLAM
LIFR-AS1
EGFLAM-AS2
LOC101929745
|
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Additional Information:
For this assay, SNP(s) [rs115572283] are located under a primer or probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.
Set Membership: |
Intragenic
Exonic
DGV Variation
|
Panther Classification:
Gene Ontology Categories:
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