Genomic Map
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Target Gene Details
Entrez Gene ID: | 83416 |
Gene Name: | Fc receptor like 5 |
Gene Aliases: |
BXMAS1, CD307, CD307e, FCRH5, IRTA2, PRO820 |
Location: |
Chr.1:157513377-157552520 on Build GRCh38 |
Assay Gene Location: | Within Intron 13 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| FCRL5 | NM_001195388.1 | NP_001182317.1 | ||
| NM_031281.2 | NP_112571.2 | |||
| XM_011510030.1 | XP_011508332.1 | |||
| XM_011510031.1 | XP_011508333.1 | |||
| XM_011510032.1 | XP_011508334.1 | |||
| AF343664.1 | AAK31327.1 | |||
| AF369794.2 | AAK50059.2 | |||
| AF397453.1 | AAK93971.1 | |||
| AK090423.1 | BAC03404.1 | |||
| AK090475.1 | BAC03456.1 | |||
| BC101066.2 | AAI01067.1 | |||
| BC101067.1 | AAI01068.1 | |||
| BC101069.2 | AAI01070.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv831681 | Chr.1:157425048 - 157527722 on Build GRCh38 | Gain+Loss |
 FCRL5
|
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Additional Information:
For this assay, SNP(s) [rs75774149] 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
|
Panther Classification:
Gene Ontology Categories:
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