Assay Details
Target Gene Details
Entrez Gene ID: | 3976 |
Gene Name: | leukemia inhibitory factor |
Gene Aliases: |
CDF, DIA, HILDA, MLPLI |
Location: |
Chr.22:30240447-30246851 on Build GRCh38 |
Assay Gene Location: | Within Exon 3 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
LIF | NM_001257135.1 | 2 | 1778 | NP_001244064.1 |
NM_002309.4 | 3 | 1957 | NP_002300.1 | |
X13967.1 | 3 | 1845 | CAA32147.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv834173 | Chr.22:30119103 - 30262288 on Build GRCh38 | Loss | MGC20647 HORMAD2 LIF |
nsv834174 | Chr.22:30223771 - 30350926 on Build GRCh38 | Gain+Loss | MGC20647 SF3A1 GATSL3 TBC1D10A LIF OSM |
nsv829171 | Chr.22:30202041 - 30647591 on Build GRCh38 | Loss | RNF215 PES1 SEC14L4 GATSL3 SDC4P SEC14L3 CCDC157 OSM MGC20647 KIAA1656 SF3A1 SEC14L6 SLC35E4 MTFP1 SEC14L2 TBC1D10A HORMAD2 GAL3ST1 TCN2 LIF |
More Information
Additional Information:
For this assay, SNP(s) [rs73881421] 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 |