Genomic Map
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Target Gene Details
Entrez Gene ID: | 57545 |
Gene Name: | coiled-coil and C2 domain containing 2A |
Gene Aliases: |
JBTS9, MKS6 |
Location: |
Chr.4:15468660-15601971 on Build GRCh38 |
Assay Gene Location: | Within Intron 7 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| CC2D2A | NM_001080522.2 | NP_001073991.2 | ||
| XM_005248177.1 | XP_005248234.1 | |||
| XM_011513872.2 | XP_011512174.1 | |||
| XM_017008482.1 | XP_016863971.1 | |||
| AB037766.1 | BAA92583.1 | |||
| AK096047.1 | ||||
| AK309178.1 | ||||
| BC103710.1 | AAI03711.1 | |||
| BX647334.1 | ||||
| DA860072.1 | ||||
| DB043556.1 | ||||
| EU450799.1 | ||||
| N35522.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| esv2759227 | Chr.4:15442993 - 15747897 on Build GRCh38 | Gain+Loss |
 FAM200B
FBXL5
CC2D2A
C1QTNF7
BST1
|
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Additional Information:
For this assay, SNP(s) [rs146899690] 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
|
Gene Ontology Categories:
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