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- Gene Symbol
- FRMD4A
- Assay Reference Genome
Location
Chr.10:13768312 on build GRCh38- Cytoband
Genomic Map
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Target Gene Details
Entrez Gene ID: | 55691 |
Gene Name: | FERM domain containing 4A |
Gene Aliases: |
CCAFCA, FRMD4, bA295P9.4 |
Location: |
Chr.10:13643706-14330924 on Build GRCh38 |
Assay Gene Location: | Within Intron 10 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| FRMD4A | NM_001318336.2 | NP_001305265.1 | ||
| NM_001318337.2 | NP_001305266.1 | |||
| NM_018027.5 | NP_060497.3 | |||
| AB037715.1 | BAA92532.2 | |||
| AK001072.1 | BAA91492.1 | |||
| AK094045.1 | ||||
| AK289693.1 | BAF82382.1 | |||
| BC151244.1 | AAI51245.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2025-12-01, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv508569 | Chr.10:13673697 - 13777350 on Build GRCh38 | Deletion |
 FRMD4A
|
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Additional Information:
For this assay, SNP(s) [rs80068779] 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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