Assay Details
Target Gene Details
Entrez Gene ID: | 54617 |
Gene Name: | INO80 complex subunit |
Gene Aliases: |
INO80A, INOC1, hINO80 |
Location: |
Chr.15:40978880-41117081 on Build GRCh38 |
Assay Gene Location: | Within Exon 37 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
INO80 | NM_017553.2 | 36 | 5074 | NP_060023.1 |
NR_104038.1 | 35 | 4946 | ||
XM_011521686.2 | 22 | 2885 | XP_011519988.1 | |
AB033085.1 | 36 | 4970 | ||
AK002176.1 | 8 | 1238 | BAA92122.1 | |
AL137280.1 | 5 | 854 | CAB70675.1 | |
BC146785.1 | 36 | 4982 | ||
BX350023.2 | 1 | 261 | ||
CB155560.1 | 1 | 244 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv1053462 | Chr.15:40977869 - 41103896 on Build GRCh38 | Gain |
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More Information
Additional Information:
For this assay, SNP(s) [rs66470529] 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: |
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Gene Ontology Categories:
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