Genomic Map
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Target Gene Details
Entrez Gene ID: | 90427 |
Gene Name: | Bcl2 modifying factor |
Gene Aliases: |
- |
Location: |
Chr.15:40087890-40108884 on Build GRCh38 |
Assay Gene Location: | Within Intron 5 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| BMF | NM_001003940.1 | NP_001003940.1 | ||
| NM_001003942.1 | NP_001003942.1 | |||
| NM_001003943.2 | NP_001003943.1 | |||
| NM_033503.3 | NP_277038.1 | |||
| AK024472.1 | ||||
| AY029254.1 | AAK38748.1 | |||
| AY222040.1 | AAP22965.1 | |||
| AY222041.1 | AAP22966.1 | |||
| BC060783.1 | AAH60783.1 | |||
| BC069328.1 | AAH69328.1 | |||
| BC069505.1 | AAH69505.1 | |||
| BC070043.1 | ||||
| BC104983.1 | AAI04984.1 | |||
| BC104985.1 | AAI04986.1 | |||
| BP280415.1 |
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Additional Information:
For this assay, SNP(s) [rs143110745] 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
non-DGV Variation
|
Gene Ontology Categories:
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