Genomic Map
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Target Gene Details
Entrez Gene ID: | 10015 |
Gene Name: | programmed cell death 6 interacting protein |
Gene Aliases: |
AIP1, ALIX, DRIP4, HP95 |
Location: |
Chr.3:33798571-33869707 on Build GRCh38 |
Assay Gene Location: | Within Intron 3 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| PDCD6IP | NM_001162429.2 | NP_001155901.1 | ||
| NM_001256192.1 | NP_001243121.1 | |||
| NM_013374.5 | NP_037506.2 | |||
| XM_011533252.1 | XP_011531554.1 | |||
| XM_011533253.1 | XP_011531555.1 | |||
| XM_017005488.1 | XP_016860977.1 | |||
| AF151793.1 | AAF08220.1 | |||
| AF250394.1 | AAQ14260.1 | |||
| AF349951.1 | AAK20398.1 | |||
| BC020066.1 | AAH20066.1 | |||
| BC068454.1 | AAH68454.1 | |||
| BT007367.1 | AAP36031.1 | |||
| DA652213.1 | ||||
| GQ131806.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv522881 | Chr.3:33694634 - 34200194 on Build GRCh38 | Gain |
 CLASP2
PDCD6IP
|
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Additional Information:
For this assay, SNP(s) [rs113387809] 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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