Genomic Map
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Target Gene Details
Entrez Gene ID: | 23022 |
Gene Name: | palladin, cytoskeletal associated protein |
Gene Aliases: |
CGI-151, CGI151, MYN, PNCA1, SIH002 |
Location: |
Chr.4:168497039-168928457 on Build GRCh38 |
Assay Gene Location: | Within Intron 1 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| PALLD | NM_001166108.1 | NP_001159580.1 | ||
| NM_016081.3 | NP_057165.3 | |||
| XM_005262861.4 | XP_005262918.1 | |||
| XM_011531768.2 | XP_011530070.1 | |||
| XM_011531769.2 | XP_011530071.1 | |||
| XM_011531770.2 | XP_011530072.1 | |||
| XM_011531771.2 | XP_011530073.1 | |||
| XM_011531772.2 | XP_011530074.1 | |||
| XM_011531773.1 | XP_011530075.1 | |||
| XM_011531774.1 | XP_011530076.1 | |||
| XM_017007910.1 | XP_016863399.1 | |||
| XM_017007911.1 | XP_016863400.1 | |||
| AF464873.1 | AAL69964.1 | |||
| BC140850.1 | ||||
| BC144666.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| esv3569818 | Chr.4:168503865 - 168506049 on Build GRCh38 | Loss |
 PALLD
|
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Set Membership: |
Intragenic
Intronic
Non-exonic
DGV Variation
|
Panther Classification:
Gene Ontology Categories:
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