Genomic Map
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Target Gene Details
Entrez Gene ID: | 10266 |
Gene Name: | receptor activity modifying protein 2 |
Gene Aliases: |
- |
Location: |
Chr.17:42761194-42763041 on Build GRCh38 |
Assay Gene Location: | Overlaps Intron 3 - Exon 4 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| RAMP2 | NM_005854.2 | NP_005845.2 | ||
| AJ001015.1 | CAA04473.1 | |||
| AL548945.3 | ||||
| AY265458.1 | AAP23299.1 | |||
| BC027975.1 | AAH27975.1 | |||
| EF687002.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv833450 | Chr.17:42660985 - 42825144 on Build GRCh38 | Loss |
 COA3
BECN1
CNTNAP1
TUBG2
VPS25
MIR6780A
CNTD1
EZH1
RAMP2
WNK4
MIR6781
CCR10
RAMP2-AS1
PLEKHH3
|
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Additional Information:
For this assay, SNP(s) [rs150879757] 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
Non-exonic
DGV Variation
|
Panther Classification:
Gene Ontology Categories:
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