Assay Details
Target Gene Details
Entrez Gene ID: | 1602 |
Gene Name: | dachshund family transcription factor 1 |
Gene Aliases: |
DACH |
Location: |
Chr.13:71437966-71868068 on Build GRCh38 |
Assay Gene Location: | Within Intron 14 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
DACH1 | NM_004392.6 | NP_004383.4 | ||
NM_080759.5 | NP_542937.3 | |||
NM_080760.5 | NP_542938.3 | |||
XM_011534939.2 | XP_011533241.1 | |||
XM_011534942.2 | XP_011533244.1 | |||
XM_017020396.1 | XP_016875885.1 | |||
AF102546.1 | AAF01351.1 | |||
AF356492.1 | AAL08487.1 | |||
AJ005670.1 | CAA06666.1 | |||
AK001000.1 | ||||
AL079278.1 | CAB45153.1 | |||
BC021219.2 | AAH21219.2 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv471153 | Chr.13:71435470 - 71473964 on Build GRCh38 | Loss | DACH1 |
nsv1038176 | Chr.13:70898018 - 71772254 on Build GRCh38 | Gain | DACH1 LINC00348 |
More Information
Additional Information:
For this assay, SNP(s) [rs79757294] 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 |