Genomic Map
Back To TopAssay Details
Target Gene Details
Entrez Gene ID: | 10529 |
Gene Name: | nebulette |
Gene Aliases: |
LASP2, LNEBL |
Location: |
Chr.10:20779973-21174187 on Build GRCh38 |
Assay Gene Location: | Within Exon 38 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| NEBL | NM_001173484.1 | 7 | 2546 | NP_001166955.1 |
| NM_006393.2 | 28 | 4823 | NP_006384.1 | |
| NM_213569.2 | 7 | 2548 | NP_998734.1 | |
| XM_005252342.4 | 27 | 4825 | XP_005252399.1 | |
| XM_005252343.4 | 26 | 4684 | XP_005252400.1 | |
| XM_005252344.4 | 27 | 4728 | XP_005252401.1 | |
| XM_011519291.2 | 30 | 4819 | XP_011517593.1 | |
| XM_017015467.1 | 30 | 4935 | XP_016870956.1 | |
| XM_017015468.1 | 31 | 4703 | XP_016870957.1 | |
| AB209311.1 | 7 | 2420 | BAD92548.1 | |
| AK096540.1 | 7 | 2170 | BAC04812.1 | |
| BC110452.1 | AAI10453.1 | |||
| BC110453.1 | AAI10454.1 | |||
| Y16241.1 | 28 | 4823 | CAA76130.1 |
Back To TopMore Information
Additional Information:
For this assay, SNP(s) [rs111346650] 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
Exonic
non-DGV Variation
|
Gene Ontology Categories:
Back To Top