SPG11 Chromosome 15

SPG11 vesicle trafficking associated, spatacsin
595 variants 595 Health Risk

Upload your DNA to see your personal genotypes for variants in SPG11.

What This Gene Does
The protein encoded by this gene is a potential transmembrane protein that is phosphorylated upon DNA damage. Defects in this gene are a cause of spastic paraplegia type 11 (SPG11). Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2009]
Associated Conditions (41)
Autism spectrum disorder
Hereditary spastic paraplegia 11
Amyotrophic lateral sclerosis type 5
Charcot-Marie-Tooth disease axonal type 2X
Spastic paraparesis
Gait disturbance
Generalized hyperreflexia
Difficulty walking
Amyotrophic lateral sclerosis
Hereditary spastic paraplegia
Malignant tumor of esophagus
Nonpapillary renal cell carcinoma
Melanoma
Hepatocellular carcinoma
Thyroid cancer
nonmedullary
1
Acute myeloid leukemia
Clear cell carcinoma of kidney
Gastric cancer
+21 more conditions
Key Variants
RS2082749902
association
Autism spectrum disorder, Autism spectrum disorder
Health Risk
RS1040633382
Conflicting classifications of pathogenicity
Hereditary spastic paraplegia 11, Amyotrophic lateral sclerosis type 5, Charcot-Marie-Tooth disease axonal type 2X
Health Risk
RS1057518874
Conflicting classifications of pathogenicity
Spastic paraparesis, Gait disturbance, Generalized hyperreflexia
Health Risk
RS111347025
Conflicting classifications of pathogenicity
Hereditary spastic paraplegia 11, Amyotrophic lateral sclerosis, Hereditary spastic paraplegia
Health Risk
RS114945876
Conflicting classifications of pathogenicity
Hereditary spastic paraplegia 11, Inborn genetic diseases, Hereditary spastic paraplegia 11
Health Risk
RS117683234
Conflicting classifications of pathogenicity
Hereditary spastic paraplegia 11, SPG11-related disorder, Hereditary spastic paraplegia 11
Health Risk
RS1256036525
Conflicting classifications of pathogenicity
Inborn genetic diseases, Hereditary spastic paraplegia 11, Inborn genetic diseases
Health Risk
RS1322622893
Conflicting classifications of pathogenicity
Inborn genetic diseases, Hereditary spastic paraplegia 11, Inborn genetic diseases
Health Risk
RS1331589550
Conflicting classifications of pathogenicity
Hereditary spastic paraplegia 11, Inborn genetic diseases, Hereditary spastic paraplegia 11
Health Risk
RS1352070054
Conflicting classifications of pathogenicity
Hereditary spastic paraplegia 11, Hereditary spastic paraplegia 11
Health Risk
RS1360895808
Conflicting classifications of pathogenicity
Hereditary spastic paraplegia 11, Hereditary spastic paraplegia 11
Health Risk
RS1379359957
Conflicting classifications of pathogenicity
Charcot-Marie-Tooth disease axonal type 2X, Hereditary spastic paraplegia 11, Inborn genetic diseases
Health Risk
All Variants (595)
RSID Category Clinical Significance Conditions
RS2141011028 Health Risk Pathogenic Hereditary spastic paraplegia 11, Hereditary spastic paraplegia 11
RS2141014662 Health Risk Pathogenic Hereditary spastic paraplegia 11, Hereditary spastic paraplegia 11
RS2141027919 Health Risk Pathogenic Hereditary spastic paraplegia 11, Hereditary spastic paraplegia 11
RS2141029118 Health Risk Pathogenic Hereditary spastic paraplegia 11, Hereditary spastic paraplegia 11
RS2141056921 Health Risk Pathogenic Hereditary spastic paraplegia 11, Hereditary spastic paraplegia 11
RS2141098660 Health Risk Pathogenic Hereditary spastic paraplegia 11, Hereditary spastic paraplegia 11
RS2141106328 Health Risk Pathogenic Hereditary spastic paraplegia 11, Hereditary spastic paraplegia 11
RS2141106403 Health Risk Pathogenic Hereditary spastic paraplegia 11, Hereditary spastic paraplegia 11
RS2141106935 Health Risk Pathogenic Hereditary spastic paraplegia 11, Hereditary spastic paraplegia 11
RS2141106983 Health Risk Pathogenic Hereditary spastic paraplegia 11, Hereditary spastic paraplegia 11
RS2141107140 Health Risk Pathogenic Hereditary spastic paraplegia 11, Hereditary spastic paraplegia 11
RS2141108180 Health Risk Pathogenic Hereditary spastic paraplegia 11, Hereditary spastic paraplegia 11
RS2141121011 Health Risk Pathogenic Hereditary spastic paraplegia 11, Hereditary spastic paraplegia 11
RS2141138155 Health Risk Pathogenic Hereditary spastic paraplegia 11, Hereditary spastic paraplegia 11
RS2141138493 Health Risk Pathogenic Hereditary spastic paraplegia 11, Hereditary spastic paraplegia 11
RS2505162652 Health Risk Pathogenic Hereditary spastic paraplegia 11, Hereditary spastic paraplegia 11
RS2505176651 Health Risk Pathogenic Hereditary spastic paraplegia 11, Hereditary spastic paraplegia 11
RS2505186780 Health Risk Pathogenic Inborn genetic diseases, Inborn genetic diseases
RS2505197931 Health Risk Pathogenic Hereditary spastic paraplegia 11, Hereditary spastic paraplegia 11
RS2505205547 Health Risk Pathogenic Hereditary spastic paraplegia 11, Hereditary spastic paraplegia 11
RS2505206459 Health Risk Pathogenic Hereditary spastic paraplegia 11, Hereditary spastic paraplegia 11
RS2505221112 Health Risk Pathogenic Hereditary spastic paraplegia 11, Hereditary spastic paraplegia 11
RS2505221225 Health Risk Pathogenic Hereditary spastic paraplegia 11, Hereditary spastic paraplegia 11
RS2505221578 Health Risk Pathogenic Hereditary spastic paraplegia 11, Hereditary spastic paraplegia 11
RS2505229607 Health Risk Pathogenic Hereditary spastic paraplegia 11, Hereditary spastic paraplegia 11
RS2505229934 Health Risk Pathogenic Hereditary spastic paraplegia 11, Hereditary spastic paraplegia 11
RS2505238309 Health Risk Pathogenic Hereditary spastic paraplegia 11, Hereditary spastic paraplegia 11
RS2505239376 Health Risk Pathogenic Hereditary spastic paraplegia 11, Hereditary spastic paraplegia 11
RS2505239464 Health Risk Pathogenic Hereditary spastic paraplegia 11, Hereditary spastic paraplegia 11
RS2505289183 Health Risk Pathogenic Hereditary spastic paraplegia 11, Hereditary spastic paraplegia 11
RS2505289244 Health Risk Pathogenic Hereditary spastic paraplegia 11, Hereditary spastic paraplegia 11
RS2505289475 Health Risk Pathogenic Hereditary spastic paraplegia 11, Hereditary spastic paraplegia 11
RS2505289556 Health Risk Pathogenic Hereditary spastic paraplegia 11, Amyotrophic lateral sclerosis type 5, Charcot-Marie-Tooth disease axonal type 2X
RS2505290665 Health Risk Pathogenic Hereditary spastic paraplegia 11, Hereditary spastic paraplegia 11
RS2505290776 Health Risk Pathogenic Hereditary spastic paraplegia 11, Hereditary spastic paraplegia 11
RS2505291205 Health Risk Pathogenic Hereditary spastic paraplegia 11, Hereditary spastic paraplegia 11
RS2505293484 Health Risk Pathogenic Hereditary spastic paraplegia 11, Hereditary spastic paraplegia 11
RS2505293700 Health Risk Pathogenic Hereditary spastic paraplegia 11, Hereditary spastic paraplegia 11
RS2505293828 Health Risk Pathogenic Hereditary spastic paraplegia 11, Hereditary spastic paraplegia 11
RS2505300929 Health Risk Pathogenic Hereditary spastic paraplegia 11, Hereditary spastic paraplegia 11
RS2505301305 Health Risk Pathogenic Hereditary spastic paraplegia 11, Hereditary spastic paraplegia 11
RS2505324418 Health Risk Pathogenic Hereditary spastic paraplegia 11, Hereditary spastic paraplegia 11
RS2505324758 Health Risk Pathogenic Hereditary spastic paraplegia 11, Hereditary spastic paraplegia 11
RS2505324800 Health Risk Pathogenic Hereditary spastic paraplegia 11, Hereditary spastic paraplegia 11
RS2505324938 Health Risk Pathogenic Hereditary spastic paraplegia 11, Hereditary spastic paraplegia 11
RS2505325601 Health Risk Pathogenic Hereditary spastic paraplegia 11, Hereditary spastic paraplegia 11
RS2505342376 Health Risk Pathogenic Hereditary spastic paraplegia 11, Hereditary spastic paraplegia 11
RS2505361735 Health Risk Pathogenic Hereditary spastic paraplegia 11, Hereditary spastic paraplegia 11
RS2505362765 Health Risk Pathogenic Hereditary spastic paraplegia 11, Hereditary spastic paraplegia 11
RS2505369647 Health Risk Pathogenic Hereditary spastic paraplegia 11, Hereditary spastic paraplegia 11
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