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- Gene Symbol
- FEZ2
- Assay Reference Genome
Location
Chr.2:36565662 on build GRCh38- Cytoband
Genomic Map
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Target Gene Details
Entrez Gene ID: | 9637 |
Gene Name: | fasciculation and elongation protein zeta 2 |
Gene Aliases: |
HUM3CL |
Location: |
Chr.2:36552258-36598168 on Build GRCh38 |
Assay Gene Location: | Within Intron 5 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| FEZ2 | NM_001042548.2 | NP_001036013.1 | ||
| NM_005102.3 | NP_005093.2 | |||
| AB076184.1 | BAD06207.1 | |||
| AB209719.1 | BAD92956.1 | |||
| AF113124.1 | AAF14865.1 | |||
| AK025274.1 | ||||
| BC089390.1 | AAH89390.1 | |||
| BC110386.1 | AAI10387.1 | |||
| BX537785.1 | CAD97842.1 | |||
| U60061.1 | AAC51283.1 | |||
| U69140.1 | AAB40661.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2025-12-01, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv6340640 | Chr.2:36562701 - 36565900 on Build GRCh38 | Deletion |
 FEZ2
|
| nsv4066559 | Chr.2:36398935 - 36738385 on Build GRCh38 | Duplication |
FEZ2
CRIM1
VIT
|
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Additional Information:
For this assay, SNP(s) [rs72868447] 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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