Genomic Map
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Target Gene Details
Entrez Gene ID: | 10400 |
Gene Name: | phosphatidylethanolamine N-methyltransferase |
Gene Aliases: |
PEAMT, PEMPT, PEMT2, PNMT |
Location: |
Chr.17:17505561-17591703 on Build GRCh38 |
Assay Gene Location: | Within Intron 6 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| PEMT | NM_001267551.1 | NP_001254480.1 | ||
| NM_001267552.1 | NP_001254481.1 | |||
| NM_007169.2 | NP_009100.2 | |||
| NM_148172.2 | NP_680477.1 | |||
| NM_148173.1 | NP_680478.1 | |||
| XM_006721418.3 | XP_006721481.2 | |||
| AB029821.1 | BAA82407.1 | |||
| AF044214.1 | AAQ13425.1 | |||
| AF113126.1 | AAF14867.1 | |||
| AF176806.1 | AAD53291.1 | |||
| AF176807.1 | AAD53292.1 | |||
| AK302251.1 | ||||
| BC000557.2 | AAH00557.1 | |||
| BC050593.1 | AAH50593.1 | |||
| BM011377.1 | ||||
| CR457099.1 | CAG33380.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv524158 | Chr.17:17516885 - 17527335 on Build GRCh38 | Loss |
 PEMT
|
| nsv523094 | Chr.17:17511903 - 17527335 on Build GRCh38 | Loss |
PEMT
|
| nsv574526 | Chr.17:17519294 - 17541055 on Build GRCh38 | Loss |
PEMT
|
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Set Membership: |
Intragenic
Intronic
Non-exonic
DGV Variation
|
Panther Classification:
Gene Ontology Categories:
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