Genomic Map
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Target Gene Details
Entrez Gene ID: | 102723885 |
Gene Name: | uncharacterized LOC102723885 |
Gene Aliases: |
- |
Location: |
Chr.7:88216660-88229768 on Build GRCh38 |
Assay Gene Location: |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| LOC102723885 |
Target Gene Details
Entrez Gene ID: | 6717 |
Gene Name: | sorcin |
Gene Aliases: |
CP-22, CP22, SCN, V19 |
Location: |
Chr.7:88205115-88226993 on Build GRCh38 |
Assay Gene Location: | Within Intron 2 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| SRI | NM_001256891.1 | NP_001243820.1 | ||
| NM_001256892.1 | NP_001243821.1 | |||
| NM_003130.3 | NP_003121.1 | |||
| NM_198901.1 | NP_944490.1 | |||
| XM_011516528.1 | XP_011514830.1 | |||
| AK129770.1 | ||||
| AK295225.1 | ||||
| AK296601.1 | ||||
| AK310366.1 | ||||
| AL039198.1 | ||||
| BC011025.1 | AAH11025.1 | |||
| BI524104.1 | ||||
| BI559592.1 | ||||
| BI597920.1 | ||||
| BM739144.1 | ||||
| DA268050.1 | ||||
| L12387.1 | AAA92155.1 | |||
| M32886.1 | AAA60588.1 |
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Additional Information:
For this assay, SNP(s) [rs77291874] 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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