Genomic Map
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Target Gene Details
Entrez Gene ID: | 84869 |
Gene Name: | carbonyl reductase 4 |
Gene Aliases: |
SDR45C1 |
Location: |
Chr.4:168894484-169010317 on Build GRCh38 |
Assay Gene Location: | Within Intron 8 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| CBR4 | XM_005263315.2 | XP_005263372.1 | ||
| XM_017008782.1 | XP_016864271.1 |
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 Exon 28 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| PALLD | NM_001166108.1 | 22 | 3673 | NP_001159580.1 |
| NM_001166109.1 | 19 | 2741 | NP_001159581.1 | |
| NM_001166110.1 | 12 | 2240 | NP_001159582.1 | |
| NM_016081.3 | 21 | 3622 | NP_057165.3 | |
| XM_005262861.4 | 22 | 4326 | XP_005262918.1 | |
| XM_005262866.2 | 21 | 3876 | XP_005262923.1 | |
| XM_011531768.2 | 23 | 4580 | XP_011530070.1 | |
| XM_011531769.2 | 22 | 4529 | XP_011530071.1 | |
| XM_011531770.2 | 24 | 4626 | XP_011530072.1 | |
| XM_011531771.2 | 21 | 4307 | XP_011530073.1 | |
| XM_011531772.2 | 20 | 4208 | XP_011530074.1 | |
| XM_011531773.1 | 22 | 3908 | XP_011530075.1 | |
| XM_011531774.1 | 21 | 3857 | XP_011530076.1 | |
| XM_011531775.1 | 21 | 3261 | XP_011530077.1 | |
| XM_017007910.1 | 23 | 4575 | XP_016863399.1 | |
| AB023209.1 | 12 | 2204 | ||
| AF077041.1 | 8 | 1690 | AAD27774.1 | |
| AF151909.1 | 8 | 1596 | AAD34146.1 | |
| AF464873.1 | 21 | 3622 | AAL69964.1 | |
| AK000845.1 | 8 | 1165 | ||
| AK025843.1 | 8 | 1167 | ||
| AK095512.1 | 19 | 2703 | ||
| AL050093.1 | 3 | 325 | CAB43265.1 | |
| BC013867.2 | 11 | 1420 | AAH13867.2 | |
| BC140850.1 | ||||
| BC144666.1 | ||||
| BX537391.1 | 5 | 524 | CAD97633.1 | |
| DB257974.1 | 3 | 241 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| esv34043 | Chr.4:168909873 - 169008517 on Build GRCh38 | Loss |
 CBR4
PALLD
|
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Set Membership: |
Intragenic
Exonic
Intronic
Non-exonic
DGV Variation
|
Panther Classification:
Gene Ontology Categories:
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