Genomic Map
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Target Gene Details
Entrez Gene ID: | 4998 |
Gene Name: | origin recognition complex subunit 1 |
Gene Aliases: |
HSORC1, ORC1L, PARC1 |
Location: |
Chr.1:52371408-52404471 on Build GRCh38 |
Assay Gene Location: | Overlaps Intron 17 - Exon 18 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| ORC1 | NM_001190818.1 | NP_001177747.1 | ||
| NM_001190819.1 | NP_001177748.1 | |||
| NM_004153.3 | NP_004144.2 | |||
| XM_011541527.2 | XP_011539829.1 | |||
| XM_017001388.1 | XP_016856877.1 | |||
| XM_017001389.1 | XP_016856878.1 | |||
| AK291909.1 | ||||
| AK303420.1 | ||||
| BC011539.1 | AAH11539.1 | |||
| U40152.1 | AAC50325.1 | |||
| U43416.1 | AAA86260.1 |
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Additional Information:
For this assay, SNP(s) [rs77077945] 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
Non-exonic
non-DGV Variation
|
Panther Classification:
Gene Ontology Categories:
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