Genomic Map
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Target Gene Details
Entrez Gene ID: | 29799 |
Gene Name: | yippee like 1 |
Gene Aliases: |
FKSG3 |
Location: |
Chr.22:21697536-21735834 on Build GRCh38 |
Assay Gene Location: | Within Exon 5 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| YPEL1 | NM_013313.4 | 5 | 704 | NP_037445.1 |
| NR_130910.1 | 5 | 1088 | ||
| AB098734.1 | 5 | 704 | BAD51375.1 | |
| AB098735.1 | 5 | 704 | BAD51376.1 | |
| AF060862.1 | 4 | 404 | AAC15461.1 | |
| AF305069.1 | 4 | 464 | AAL09353.1 | |
| AW006162.1 | 1 | 308 | ||
| BC034486.1 | 5 | 562 | AAH34486.1 | |
| BC074501.1 | 5 | 569 | AAH74501.1 | |
| BI461654.1 | 5 | 761 | ||
| BI559478.1 | 5 | 584 | ||
| CR456376.2 | 4 | 351 | CAG30262.1 | |
| CR933630.1 | 4 | 4807 | CAI45937.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv191511 | Chr.22:21698277 - 21704496 on Build GRCh38 | Deletion |
 YPEL1
|
| nsv510804 | Chr.22:21670242 - 21778475 on Build GRCh38 | Deletion |
YPEL1
PPIL2
MAPK1
|
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Additional Information:
For this assay, SNP(s) [rs78391197] 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
|
Gene Ontology Categories:
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