Assay Details
Target Gene Details
Entrez Gene ID: | 3229 |
Gene Name: | homeobox C13 |
Gene Aliases: |
ECTD9, HOX3, HOX3G |
Location: |
Chr.12:53938792-53946544 on Build GRCh38 |
Assay Gene Location: | Within Intron 1 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| HOXC13 | NM_017410.2 | NP_059106.2 | ||
| AF255676.1 | AAF67760.1 | |||
| AF263466.2 | AAF73439.1 | |||
| AK024027.1 | BAB14786.1 | |||
| BC090850.1 | AAH90850.1 | |||
| BT009908.1 | AAP88910.1 | |||
| BU158600.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv826379 | Chr.12:53935085 - 54056069 on Build GRCh38 | Gain |
|
More Information
Additional Information:
For this assay, SNP(s) [rs79833984] 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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Genomic Map