Genomic Map
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Target Gene Details
Entrez Gene ID: | 79993 |
Gene Name: | ELOVL fatty acid elongase 7 |
Gene Aliases: |
- |
Location: |
Chr.5:60751789-60844292 on Build GRCh38 |
Assay Gene Location: | Within Exon 15 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| ELOVL7 | NM_001104558.1 | 8 | 1821 | NP_001098028.1 |
| NM_001297617.1 | 11 | 2219 | NP_001284546.1 | |
| NM_001297618.1 | 9 | 1826 | NP_001284547.1 | |
| NM_024930.2 | 9 | 1872 | NP_079206.2 | |
| XM_005248606.4 | 8 | 2436 | XP_005248663.1 | |
| XM_005248607.3 | 9 | 2149 | XP_005248664.1 | |
| XM_006714695.3 | 10 | 1928 | XP_006714758.1 | |
| XM_011543651.2 | 10 | 2118 | XP_011541953.1 | |
| XM_017009885.1 | 9 | 1809 | XP_016865374.1 | |
| XM_017009886.1 | 11 | 2048 | XP_016865375.1 | |
| XM_017009887.1 | 11 | 2239 | XP_016865376.1 | |
| AB181393.1 | 9 | 1813 | BAD93238.1 | |
| AK027216.1 | 7 | 1642 | BAB15697.1 | |
| AL137506.1 | 4 | 1303 | CAB70777.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| esv2763456 | Chr.5:60711528 - 60855940 on Build GRCh38 | Loss |
 ELOVL7
|
| esv3894195 | Chr.5:60697464 - 60793609 on Build GRCh38 | Loss |
ELOVL7
DEPDC1B
|
| nsv1023403 | Chr.5:60673707 - 60783995 on Build GRCh38 | Gain |
ELOVL7
DEPDC1B
|
| nsv598298 | Chr.5:60673188 - 60820786 on Build GRCh38 | Loss |
ELOVL7
DEPDC1B
|
| esv2752073 | Chr.5:60738648 - 60840799 on Build GRCh38 | Loss |
ELOVL7
|
| nsv4851 | Chr.5:60741337 - 60765578 on Build GRCh38 | Insertion |
ELOVL7
|
| nsv508362 | Chr.5:60694481 - 60755067 on Build GRCh38 | Deletion |
ELOVL7
DEPDC1B
|
Back To TopMore Information
Set Membership: |
Intragenic
Exonic
DGV Variation
|
Panther Classification:
Gene Ontology Categories:
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