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- Gene Symbol
- CDH2
- Assay Reference Genome
Location
Chr.18:28149502 on build GRCh38- Cytoband
- 18q12.1
Genomic Map
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Target Gene Details
Entrez Gene ID: | 1000 |
Gene Name: | cadherin 2 |
Gene Aliases: |
CD325, CDHN, CDw325, NCAD |
Location: |
Chr.18:27932878-28177446 on Build GRCh38 |
Assay Gene Location: | Within Intron 2 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| CDH2 | NM_001792.4 | NP_001783.2 | ||
| XM_011525788.1 | XP_011524090.1 | |||
| XM_017025514.1 | XP_016881003.1 | |||
| AI752180.1 | ||||
| BC036470.1 | AAH36470.1 | |||
| CN263272.1 | ||||
| DA225616.1 | ||||
| S42303.1 | AAB22854.1 | |||
| X54315.1 | CAA38213.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv1059472 | Chr.18:27276596 - 28749090 on Build GRCh38 | Gain |
 CDH2
LOC105372038
|
| esv2761996 | Chr.18:27286119 - 28238654 on Build GRCh38 | Loss |
CDH2
LOC105372038
|
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Additional Information:
For this assay, SNP(s) [rs75084177] 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
|
Panther Classification:
Gene Ontology Categories:
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