Assay Details
Target Gene Details
Entrez Gene ID: | 441549 |
Gene Name: | cerebral dopamine neurotrophic factor |
Gene Aliases: |
ARMETL1 |
Location: |
Chr.10:14819245-14838073 on Build GRCh38 |
Assay Gene Location: | Within Intron 3 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
CDNF | NM_001029954.2 | NP_001025125.2 | ||
XM_011519488.2 | XP_011517790.1 | |||
BC037872.1 | AAH37872.1 | |||
BC133042.1 | ||||
BC133044.1 | ||||
CN311321.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv471664 | Chr.10:14676176 - 14826378 on Build GRCh38 | Gain+Loss | FAM107B CDNF |
nsv1043133 | Chr.10:14711571 - 14869583 on Build GRCh38 | Loss | FAM107B CDNF HSPA14 |
nsv5899 | Chr.10:14803505 - 14837648 on Build GRCh38 | Insertion | CDNF |
More Information
Additional Information:
For this assay, SNP(s) [rs117718719] 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 Intronic Non-exonic DGV Variation |