Genomic Map
Back To TopAssay Details
Target Gene Details
Entrez Gene ID: | 5629 |
Gene Name: | prospero homeobox 1 |
Gene Aliases: |
- |
Location: |
Chr.1:213983239-214041510 on Build GRCh38 |
Assay Gene Location: | Within Intron 6 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| PROX1 | NM_001270616.1 | NP_001257545.1 | ||
| NM_002763.4 | NP_002754.2 | |||
| XM_005273194.1 | XP_005273251.1 | |||
| XM_005273195.4 | XP_005273252.1 | |||
| XM_011509771.1 | XP_011508073.1 | |||
| XM_011509772.2 | XP_011508074.1 | |||
| XM_011509773.2 | XP_011508075.1 | |||
| XM_017001832.1 | XP_016857321.1 | |||
| XM_017001833.1 | XP_016857322.1 | |||
| AK298182.1 | ||||
| BC024201.2 | AAH24201.1 | |||
| U44060.1 | AAC50656.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv4498 | Chr.1:213981463 - 214016219 on Build GRCh38 | Insertion |
 PROX1
PROX1-AS1
|
Back To TopMore Information
Additional Information:
For this assay, SNP(s) [rs117353249] 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:
Back To Top