Genomic Map
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Target Gene Details
Entrez Gene ID: | 25936 |
Gene Name: | NSL1, MIS12 kinetochore complex component |
Gene Aliases: |
C1orf48, DC8, MIS14 |
Location: |
Chr.1:212726153-212798900 on Build GRCh38 |
Assay Gene Location: | Within Exon 9 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| NSL1 | NM_001042549.1 | 7 | 10709 | NP_001036014.1 |
| NM_001297736.1 | 4 | 10501 | NP_001284665.1 | |
| NM_001297737.1 | 5 | 10556 | NP_001284666.1 | |
| NM_001297739.1 | NP_001284668.1 | |||
| NM_015471.3 | 6 | 10624 | NP_056286.3 | |
| AI703127.1 | ||||
| AK092359.1 | 1 | 388 | ||
| AK124596.1 | 1 | 1122 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv549148 | Chr.1:212703560 - 212788865 on Build GRCh38 | Loss |
 NSL1
|
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Additional Information:
For this assay, SNP(s) [rs74138622] 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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