Assay Details
Target Gene Details
Entrez Gene ID: | 102723508 |
Gene Name: | KDM5C adjacent non-coding transcript |
Gene Aliases: |
LINC01155, Spasm |
Location: |
Chr.X:53094157-53144072 on Build GRCh38 |
Assay Gene Location: | Within Intron 2 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| KANTR | NR_110456.1 | |||
| AL599773.1 | ||||
| BX353482.2 | ||||
| CF994433.1 | ||||
| EF565109.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv508773 | Chr.X:53034408 - 53141410 on Build GRCh38 | Insertion |
|
| esv2740175 | Chr.X:52862926 - 55652533 on Build GRCh38 | Deletion |
|
| nsv435891 | Chr.X:52861979 - 55653313 on Build GRCh38 | Deletion |
|
More Information
Additional Information:
For this assay, SNP(s) [rs79055434] 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: |
|

Genomic Map