Genomic Map
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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 Intron 39 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| SPG11 | NM_001160227.1 | NP_001153699.1 | ||
| NM_025137.3 | NP_079413.3 | |||
| XM_006720700.1 | XP_006720763.1 | |||
| XM_017022634.1 | XP_016878123.1 | |||
| XM_017022636.1 | XP_016878125.1 | |||
| AB058743.2 | BAB47469.2 | |||
| AB470308.1 | ||||
| AB470309.1 | ||||
| AB470310.1 | ||||
| AK025092.1 | BAB15065.1 | |||
| AK057869.1 | ||||
| AK225186.1 | ||||
| BC024161.1 | ||||
| BC067798.1 | AAH67798.1 | |||
| BC094704.1 | AAH94704.1 | |||
| BC150640.1 | ||||
| BC153879.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv827313 | Chr.15:44565158 - 44571284 on Build GRCh38 | Loss |
 SPG11
|
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Set Membership: |
Intragenic
Intronic
Non-exonic
DGV Variation
|
Gene Ontology Categories:
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