Assay Details
Target Gene Details
Entrez Gene ID: | 55954 |
Gene Name: | zinc finger matrin-type 5 |
Gene Aliases: |
SNRNP20, U11/U12-20K, ZC3H19 |
Location: |
Chr.22:29730956-29767011 on Build GRCh38 |
Assay Gene Location: | Within Intron 6 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
ZMAT5 | NM_001003692.1 | NP_001003692.1 | ||
NM_001318129.1 | NP_001305058.1 | |||
NM_019103.2 | NP_061976.1 | |||
AK292671.1 | ||||
AL160311.1 | CAB77284.1 | |||
BC009717.1 | AAH09717.1 | |||
BG285784.1 | ||||
BQ931527.1 | ||||
BU598307.1 | ||||
CR456353.1 | CAG30239.1 | |||
CR457393.1 | CAG33674.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv515720 | Chr.22:29685726 - 29767537 on Build GRCh38 | Gain+Loss | CABP7 NF2 ZMAT5 UQCR10 |
More Information
Additional Information:
For this assay, SNP(s) [rs115982059,rs73390974] 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 |