Genomic Map
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Target Gene Details
Entrez Gene ID: | 23322 |
Gene Name: | RPGRIP1 like |
Gene Aliases: |
CORS3, FTM, JBTS7, MKS5, NPHP8, PPP1R134 |
Location: |
Chr.16:53599239-53703934 on Build GRCh38 |
Assay Gene Location: | Within Intron 29 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| RPGRIP1L | XM_005255867.1 | XP_005255924.1 | ||
| XM_005255868.1 | XP_005255925.1 | |||
| XM_017023094.1 | XP_016878583.1 | |||
| XM_017023095.1 | XP_016878584.1 | |||
| XM_017023096.1 | XP_016878585.1 | |||
| XM_017023098.1 | XP_016878587.1 | |||
| XM_017023099.1 | XP_016878588.1 | |||
| AB023222.1 | BAA76849.1 | |||
| AK026552.1 | ||||
| AK304790.1 | ||||
| AK307929.1 | ||||
| BC136433.1 | ||||
| CR749645.1 | CAH18439.1 |
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Additional Information:
For this assay, SNP(s) [rs78029223] 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
non-DGV Variation
|
Panther Classification:
Gene Ontology Categories:
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