Genomic Map
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Target Gene Details
Entrez Gene ID: | 9848 |
Gene Name: | microfibrillar associated protein 3 like |
Gene Aliases: |
NYD-sp9 |
Location: |
Chr.4:169986597-170033028 on Build GRCh38 |
Assay Gene Location: | Within Intron 9 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| MFAP3L | NM_001009554.3 | NP_001009554.1 | ||
| NM_001301647.1 | NP_001288576.1 | |||
| NM_001301648.1 | NP_001288577.1 | |||
| NM_021647.7 | NP_067679.6 | |||
| XM_005263366.3 | XP_005263423.1 | |||
| XM_017008864.1 | XP_016864353.1 | |||
| XM_017008865.1 | XP_016864354.1 | |||
| XM_017008866.1 | XP_016864355.1 | |||
| XM_017008867.1 | XP_016864356.1 | |||
| XM_017008868.1 | XP_016864357.1 | |||
| XM_017008869.1 | XP_016864358.1 | |||
| XM_017008870.1 | XP_016864359.1 | |||
| XM_017008871.1 | XP_016864360.1 | |||
| AB014526.1 | ||||
| AF327560.1 | AAK15700.1 | |||
| AK290041.1 | ||||
| AK308263.1 | ||||
| AY391838.1 | AAS55434.1 | |||
| BC066912.1 | AAH66912.1 | |||
| BI459190.1 | ||||
| BM552945.1 | ||||
| DA412844.1 | ||||
| DB026038.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| esv3603133 | Chr.4:169999442 - 170001794 on Build GRCh38 | Loss |
 MFAP3L
|
| esv2661256 | Chr.4:169999364 - 170001774 on Build GRCh38 | Deletion |
MFAP3L
|
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Additional Information:
For this assay, SNP(s) [rs73864512] 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
|
Gene Ontology Categories:
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