Genomic Map
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Target Gene Details
Entrez Gene ID: | 10445 |
Gene Name: | microspherule protein 1 |
Gene Aliases: |
ICP22BP, INO80Q, MCRS2, MSP58, P78 |
Location: |
Chr.12:49558294-49572157 on Build GRCh38 |
Assay Gene Location: | Within Exon 16 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| MCRS1 | NM_001012300.1 | 14 | 1582 | NP_001012300.1 |
| NM_001278341.1 | 13 | 1492 | NP_001265270.1 | |
| NM_006337.4 | 15 | 1751 | NP_006328.2 | |
| XM_005268572.3 | 16 | 1851 | XP_005268629.1 | |
| XM_011537760.2 | 14 | 5643 | XP_011536062.1 | |
| XM_017018689.1 | 15 | 2087 | XP_016874178.1 | |
| XM_017018690.1 | 16 | 2172 | XP_016874179.1 | |
| AF015308.1 | 14 | 1659 | AAC52086.1 | |
| AF068007.1 | 14 | 2291 | AAC68599.1 | |
| BC011794.2 | 15 | 1734 | AAH11794.1 | |
| BX538079.1 | 13 | 1479 | CAD98003.1 | |
| R66413.1 | 1 | 211 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv832406 | Chr.12:49466910 - 49668353 on Build GRCh38 | Loss |
 KCNH3
FAM186B
MCRS1
LOC100422296
FMNL3
PRPF40B
SPATS2
|
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Additional Information:
For this assay, SNP(s) [rs144315524] 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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