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
RS1337761270 Health Risk Pathogenic Hereditary spastic paraplegia 11, Hereditary spastic paraplegia 11
RS1339135039 Health Risk Pathogenic Hereditary spastic paraplegia 11, Hereditary spastic paraplegia 11
RS1363959441 Health Risk Pathogenic Hereditary spastic paraplegia 11, Hereditary spastic paraplegia 11
RS1366914385 Health Risk Pathogenic Hereditary spastic paraplegia 11, Hereditary spastic paraplegia 11
RS138103656 Health Risk Pathogenic Hereditary spastic paraplegia 11, Hereditary spastic paraplegia 11
RS1381237268 Health Risk Pathogenic
RS1397432412 Health Risk Pathogenic Hereditary spastic paraplegia 11, Hereditary spastic paraplegia 11
RS140385286 Health Risk Pathogenic Hereditary spastic paraplegia 11, Amyotrophic lateral sclerosis type 5, Charcot-Marie-Tooth disease axonal type 2X
RS141848292 Health Risk Pathogenic Hereditary spastic paraplegia 11, Inborn genetic diseases, Charcot-Marie-Tooth disease axonal type 2X
RS1422477670 Health Risk Pathogenic Hereditary spastic paraplegia 11, Amyotrophic lateral sclerosis type 5, Charcot-Marie-Tooth disease axonal type 2X
RS1432604396 Health Risk Pathogenic Hereditary spastic paraplegia 11, Hereditary spastic paraplegia 11
RS1439018038 Health Risk Pathogenic Hereditary spastic paraplegia 11, Hereditary spastic paraplegia 11
RS1440947266 Health Risk Pathogenic Hereditary spastic paraplegia 11, Hereditary spastic paraplegia 11
RS1442912535 Health Risk Pathogenic Hereditary spastic paraplegia 11, Hereditary spastic paraplegia 11
RS1454768655 Health Risk Pathogenic Hereditary spastic paraplegia 11, Hereditary spastic paraplegia 11, Hereditary spastic paraplegia
RS146098780 Health Risk Pathogenic Hereditary spastic paraplegia 11, Hereditary spastic paraplegia 11
RS1462607878 Health Risk Pathogenic Hereditary spastic paraplegia, Hereditary spastic paraplegia 11, Hereditary spastic paraplegia
RS1470463921 Health Risk Pathogenic Hereditary spastic paraplegia 11, Hereditary spastic paraplegia, Hereditary spastic paraplegia 11
RS1470512931 Health Risk Pathogenic Hereditary spastic paraplegia 11, Hereditary spastic paraplegia 11
RS1473836469 Health Risk Pathogenic Hereditary spastic paraplegia 11, Hereditary spastic paraplegia, Hereditary spastic paraplegia 11
RS1476614745 Health Risk Pathogenic Hereditary spastic paraplegia 11, Thyroid cancer, nonmedullary
RS147713329 Health Risk Pathogenic Hereditary spastic paraplegia 11, Amyotrophic lateral sclerosis type 5, Hereditary spastic paraplegia
RS1482197593 Health Risk Pathogenic Hereditary spastic paraplegia 11, Hereditary spastic paraplegia 11
RS1488708341 Health Risk Pathogenic
RS1555381616 Health Risk Pathogenic Hereditary spastic paraplegia 11, Hereditary spastic paraplegia 11
RS1555446712 Health Risk Pathogenic Hereditary spastic paraplegia 11, Hereditary spastic paraplegia 11, Hereditary spastic paraplegia 11
RS1555447724 Health Risk Pathogenic Hereditary spastic paraplegia 11, Hereditary spastic paraplegia 11
RS1555448810 Health Risk Pathogenic Hereditary spastic paraplegia 11, Hereditary spastic paraplegia 11
RS1555450825 Health Risk Pathogenic Hereditary spastic paraplegia 11, Hereditary spastic paraplegia 11
RS1555451491 Health Risk Pathogenic
RS1555451983 Health Risk Pathogenic
RS1555454508 Health Risk Pathogenic Hereditary spastic paraplegia 11, Hereditary spastic paraplegia 11
RS1555455246 Health Risk Pathogenic Hereditary spastic paraplegia 11, Hereditary spastic paraplegia 11
RS1555455266 Health Risk Pathogenic Hereditary spastic paraplegia 11, Hereditary spastic paraplegia 11
RS1555456457 Health Risk Pathogenic
RS1566838280 Health Risk Pathogenic Inborn genetic diseases, Inborn genetic diseases
RS1567127243 Health Risk Pathogenic Hereditary spastic paraplegia 11, Hereditary spastic paraplegia 11
RS1567129475 Health Risk Pathogenic Hereditary spastic paraplegia 11, Hereditary spastic paraplegia 11
RS1567131767 Health Risk Pathogenic Hereditary spastic paraplegia 11, Hereditary spastic paraplegia 11
RS1567138536 Health Risk Pathogenic Hereditary spastic paraplegia 11, Hereditary spastic paraplegia 11
RS1595842556 Health Risk Pathogenic Hereditary spastic paraplegia 11, Hereditary spastic paraplegia 11
RS1595865855 Health Risk Pathogenic Hereditary spastic paraplegia 11, Hereditary spastic paraplegia 11
RS1595878941 Health Risk Pathogenic Hereditary spastic paraplegia 11, Hereditary spastic paraplegia 11
RS1595898030 Health Risk Pathogenic Hereditary spastic paraplegia 11, Hereditary spastic paraplegia 11
RS1595898055 Health Risk Pathogenic Hereditary spastic paraplegia 11, Hereditary spastic paraplegia 11
RS1595898078 Health Risk Pathogenic Hereditary spastic paraplegia 11, Hereditary spastic paraplegia 11
RS1595935001 Health Risk Pathogenic Hereditary spastic paraplegia 11, Hereditary spastic paraplegia 11
RS1595938132 Health Risk Pathogenic Hereditary spastic paraplegia 11, Hereditary spastic paraplegia 11
RS1595940058 Health Risk Pathogenic Hereditary spastic paraplegia 11, Hereditary spastic paraplegia 11
RS1595940106 Health Risk Pathogenic Hereditary spastic paraplegia 11, Hereditary spastic paraplegia 11
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