Genomic Map
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Target Gene Details
Entrez Gene ID: | 1719 |
Gene Name: | dihydrofolate reductase |
Gene Aliases: |
DHFRP1, DYR |
Location: |
Chr.5:80626226-80654981 on Build GRCh38 |
Assay Gene Location: | Within Intron 5 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| DHFR | NM_000791.3 | NP_000782.1 | ||
| NM_001290354.1 | NP_001277283.1 | |||
| NM_001290357.1 | NP_001277286.1 | |||
| NR_110936.1 | ||||
| AK293146.1 | ||||
| AK297302.1 | ||||
| AK308492.1 | ||||
| BC000192.1 | AAH00192.1 | |||
| BC003584.1 | AAH03584.2 | |||
| BC070280.1 | AAH70280.1 | |||
| BC071996.1 | AAH71996.1 | |||
| J00140.1 | AAA58485.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv483112 | Chr.5:80551019 - 80731514 on Build GRCh38 | Loss |
 ANKRD34B
DHFR
LINC01337
MTRNR2L2
MSH3
|
| nsv4895 | Chr.5:80623591 - 80640149 on Build GRCh38 | Insertion |
DHFR
|
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Additional Information:
For this assay, SNP(s) [rs202167641] 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
Intronic
Non-exonic
DGV Variation
|
Panther Classification:
Gene Ontology Categories:
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