ATL1 Chromosome 14

Atlastin GTPase 1
111 variants 111 Health Risk

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What This Gene Does
The protein encoded by this gene is a GTPase and a Golgi body transmembrane protein. The encoded protein can form a homotetramer and has been shown to interact with spastin and with mitogen-activated protein kinase kinase kinase kinase 4. This protein may be involved in axonal maintenance as evidenced by the fact that defects in this gene are a cause of spastic paraplegia type 3. Three transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
Gene Info
Gene Group
Atlastins
Locus Type
gene with protein product
Location
14q22.1
Ensembl
ENSG00000198513
Associated Conditions (19)
Hereditary spastic paraplegia 3A
Abnormal pyramidal sign
Inborn genetic diseases
ATL1-related disorder
Hereditary spastic paraplegia
Neuropathy
hereditary sensory
type 1D
Charcot-Marie-Tooth disease
Abnormality of the nervous system
Spastic paraplegia
Accessory ectopic thyroid tissue
Neurodevelopmental delay
ATL1-related spastic paraplegia
recessive
Osteomyelitis leading to amputation due to slow healing fractures
Penetrating foot ulcers
Distal sensory impairment
Distal lower limb muscle weakness
Key Variants
RS1060502971
Conflicting classifications of pathogenicity
Hereditary spastic paraplegia 3A, Abnormal pyramidal sign, Hereditary spastic paraplegia 3A
Health Risk
RS112496709
Conflicting classifications of pathogenicity
Hereditary spastic paraplegia 3A, Inborn genetic diseases, Hereditary spastic paraplegia 3A
Health Risk
RS1181733510
Conflicting classifications of pathogenicity
Hereditary spastic paraplegia 3A, Hereditary spastic paraplegia 3A
Health Risk
RS119476047
Conflicting classifications of pathogenicity
Hereditary spastic paraplegia 3A, Hereditary spastic paraplegia 3A, Hereditary spastic paraplegia 3A
Health Risk
RS1395551564
Conflicting classifications of pathogenicity
Hereditary spastic paraplegia 3A, Inborn genetic diseases, Hereditary spastic paraplegia 3A
Health Risk
RS1402672430
Conflicting classifications of pathogenicity
Hereditary spastic paraplegia 3A, Hereditary spastic paraplegia 3A
Health Risk
RS144792471
Conflicting classifications of pathogenicity
Hereditary spastic paraplegia 3A, Inborn genetic diseases, Hereditary spastic paraplegia 3A
Health Risk
RS147839037
Conflicting classifications of pathogenicity
Hereditary spastic paraplegia 3A, Inborn genetic diseases, ATL1-related disorder
Health Risk
RS1555363969
Conflicting classifications of pathogenicity
Hereditary spastic paraplegia 3A, Hereditary spastic paraplegia 3A
Health Risk
RS1555364149
Conflicting classifications of pathogenicity
Hereditary spastic paraplegia 3A, Hereditary spastic paraplegia 3A
Health Risk
RS1555364246
Conflicting classifications of pathogenicity
Hereditary spastic paraplegia 3A, Hereditary spastic paraplegia 3A
Health Risk
RS1595615134
Conflicting classifications of pathogenicity
Hereditary spastic paraplegia 3A, Hereditary spastic paraplegia 3A
Health Risk
All Variants (111)
RSID Category Clinical Significance Conditions
RS1060502971 Health Risk Conflicting classifications of pathogenicity Hereditary spastic paraplegia 3A, Abnormal pyramidal sign, Hereditary spastic paraplegia 3A
RS112496709 Health Risk Conflicting classifications of pathogenicity Hereditary spastic paraplegia 3A, Inborn genetic diseases, Hereditary spastic paraplegia 3A
RS1181733510 Health Risk Conflicting classifications of pathogenicity Hereditary spastic paraplegia 3A, Hereditary spastic paraplegia 3A
RS119476047 Health Risk Conflicting classifications of pathogenicity Hereditary spastic paraplegia 3A, Hereditary spastic paraplegia 3A, Hereditary spastic paraplegia 3A
RS1395551564 Health Risk Conflicting classifications of pathogenicity Hereditary spastic paraplegia 3A, Inborn genetic diseases, Hereditary spastic paraplegia 3A
RS1402672430 Health Risk Conflicting classifications of pathogenicity Hereditary spastic paraplegia 3A, Hereditary spastic paraplegia 3A
RS144792471 Health Risk Conflicting classifications of pathogenicity Hereditary spastic paraplegia 3A, Inborn genetic diseases, Hereditary spastic paraplegia 3A
RS147839037 Health Risk Conflicting classifications of pathogenicity Hereditary spastic paraplegia 3A, Inborn genetic diseases, ATL1-related disorder
RS1555363969 Health Risk Conflicting classifications of pathogenicity Hereditary spastic paraplegia 3A, Hereditary spastic paraplegia 3A
RS1555364149 Health Risk Conflicting classifications of pathogenicity Hereditary spastic paraplegia 3A, Hereditary spastic paraplegia 3A
RS1555364246 Health Risk Conflicting classifications of pathogenicity Hereditary spastic paraplegia 3A, Hereditary spastic paraplegia 3A
RS1595615134 Health Risk Conflicting classifications of pathogenicity Hereditary spastic paraplegia 3A, Hereditary spastic paraplegia 3A
RS1595619553 Health Risk Conflicting classifications of pathogenicity Neuropathy, hereditary sensory, type 1D
RS1595620366 Health Risk Conflicting classifications of pathogenicity Hereditary spastic paraplegia 3A, Hereditary spastic paraplegia 3A
RS1595625010 Health Risk Conflicting classifications of pathogenicity Hereditary spastic paraplegia 3A, Hereditary spastic paraplegia 3A
RS186528086 Health Risk Conflicting classifications of pathogenicity Hereditary spastic paraplegia 3A, ATL1-related disorder, Hereditary spastic paraplegia 3A
RS200314808 Health Risk Conflicting classifications of pathogenicity Neuropathy, hereditary sensory, type 1D
RS2039208042 Health Risk Conflicting classifications of pathogenicity Hereditary spastic paraplegia 3A, Hereditary spastic paraplegia 3A, Hereditary spastic paraplegia 3A
RS2039539644 Health Risk Conflicting classifications of pathogenicity Hereditary spastic paraplegia, Hereditary spastic paraplegia 3A, Hereditary spastic paraplegia
RS2140226921 Health Risk Conflicting classifications of pathogenicity Hereditary spastic paraplegia 3A, Hereditary spastic paraplegia 3A
RS2140234793 Health Risk Conflicting classifications of pathogenicity Hereditary spastic paraplegia 3A, Hereditary spastic paraplegia 3A
RS2140239163 Health Risk Conflicting classifications of pathogenicity Hereditary spastic paraplegia 3A, Hereditary spastic paraplegia 3A
RS2140239426 Health Risk Conflicting classifications of pathogenicity Hereditary spastic paraplegia 3A, Hereditary spastic paraplegia 3A
RS2504577368 Health Risk Conflicting classifications of pathogenicity Hereditary spastic paraplegia 3A, Hereditary spastic paraplegia 3A, Hereditary spastic paraplegia 3A
RS2504578020 Health Risk Conflicting classifications of pathogenicity Hereditary spastic paraplegia 3A, Hereditary spastic paraplegia 3A
RS372029461 Health Risk Conflicting classifications of pathogenicity Hereditary spastic paraplegia 3A, Inborn genetic diseases, Hereditary spastic paraplegia 3A
RS373267047 Health Risk Conflicting classifications of pathogenicity Hereditary spastic paraplegia 3A, Inborn genetic diseases, Hereditary spastic paraplegia 3A
RS377127492 Health Risk Conflicting classifications of pathogenicity Hereditary spastic paraplegia 3A, Inborn genetic diseases, Hereditary spastic paraplegia 3A
RS377736535 Health Risk Conflicting classifications of pathogenicity Hereditary spastic paraplegia 3A, Hereditary spastic paraplegia 3A
RS387906941 Health Risk Conflicting classifications of pathogenicity Hereditary spastic paraplegia 3A, Hereditary spastic paraplegia, Inborn genetic diseases
RS397514712 Health Risk Conflicting classifications of pathogenicity Hereditary spastic paraplegia 3A, Hereditary spastic paraplegia 3A
RS749993404 Health Risk Conflicting classifications of pathogenicity Hereditary spastic paraplegia 3A, Inborn genetic diseases, Hereditary spastic paraplegia 3A
RS752593199 Health Risk Conflicting classifications of pathogenicity Hereditary spastic paraplegia 3A, Inborn genetic diseases, Hereditary spastic paraplegia 3A
RS763169900 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Hereditary spastic paraplegia 3A, Inborn genetic diseases
RS771031586 Health Risk Conflicting classifications of pathogenicity Hereditary spastic paraplegia 3A, Inborn genetic diseases, Hereditary spastic paraplegia 3A
RS771568686 Health Risk Conflicting classifications of pathogenicity Hereditary spastic paraplegia 3A, Hereditary spastic paraplegia 3A
RS772206990 Health Risk Conflicting classifications of pathogenicity Hereditary spastic paraplegia 3A, Inborn genetic diseases, Hereditary spastic paraplegia 3A
RS773401705 Health Risk Conflicting classifications of pathogenicity Neuropathy, hereditary sensory, type 1D
RS777479928 Health Risk Conflicting classifications of pathogenicity Hereditary spastic paraplegia 3A, Inborn genetic diseases, Hereditary spastic paraplegia 3A
RS863223314 Health Risk Conflicting classifications of pathogenicity Hereditary spastic paraplegia 3A, Hereditary spastic paraplegia 3A
RS863224772 Health Risk Conflicting classifications of pathogenicity Hereditary spastic paraplegia 3A, Inborn genetic diseases, Hereditary spastic paraplegia 3A
RS864622520 Health Risk Conflicting classifications of pathogenicity Hereditary spastic paraplegia 3A, Hereditary spastic paraplegia, Hereditary spastic paraplegia 3A
RS886041897 Health Risk Conflicting classifications of pathogenicity Hereditary spastic paraplegia 3A, Hereditary spastic paraplegia 3A
RS985551666 Health Risk Conflicting classifications of pathogenicity Hereditary spastic paraplegia 3A, Hereditary spastic paraplegia 3A
RS1033998490 Health Risk Likely pathogenic
RS1064795212 Health Risk Likely pathogenic Hereditary spastic paraplegia 3A, Abnormality of the nervous system, Hereditary spastic paraplegia 3A
RS1241621325 Health Risk Likely pathogenic Hereditary spastic paraplegia 3A, Hereditary spastic paraplegia 3A, Spastic paraplegia
RS1555364153 Health Risk Likely pathogenic
RS1555364247 Health Risk Likely pathogenic Hereditary spastic paraplegia 3A, Hereditary spastic paraplegia 3A
RS1555365512 Health Risk Likely pathogenic Hereditary spastic paraplegia 3A, Hereditary spastic paraplegia 3A, Hereditary spastic paraplegia 3A
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