Assay Details
Target Gene Details
Entrez Gene ID: | 80208 |
Gene Name: | spastic paraplegia 11 (autosomal recessive) |
Gene Aliases: |
ALS5, CMT2X, KIAA1840 |
Location: |
Chr.15:44562696-44663678 on Build GRCh38 |
Assay Gene Location: | Within Exon 40 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
SPG11 | NM_001160227.1 | 37 | 6750 | NP_001153699.1 |
NM_025137.3 | 39 | 7089 | NP_079413.3 | |
XM_006720700.1 | 39 | 6945 | XP_006720763.1 | |
XM_017022634.1 | 38 | 6981 | XP_016878123.1 | |
XM_017022636.1 | 28 | 4898 | XP_016878125.1 | |
AB058743.2 | 39 | 7059 | BAB47469.2 | |
AB470308.1 | ||||
AB470309.1 | 39 | 7058 | ||
AB470310.1 | 39 | 7058 | ||
AK025092.1 | 10 | 1210 | BAB15065.1 | |
AK057869.1 | 7 | 1429 | ||
AK225186.1 | 10 | 1210 | ||
BC024161.1 | 9 | 1175 | ||
BC067798.1 | 10 | 1451 | AAH67798.1 | |
BC094704.1 | 10 | 1583 | AAH94704.1 | |
BC150640.1 | 37 | 6747 | ||
BC153879.1 | 39 | 7059 |
More Information
Additional Information:
For this assay, SNP(s) [rs80338869] 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 |