ASAH1 Chromosome 8

N-acylsphingosine amidohydrolase 1
123 variants 123 Health Risk

Upload your DNA to see your personal genotypes for variants in ASAH1.

What This Gene Does
This gene encodes a member of the acid ceramidase family of proteins. Alternative splicing results in multiple transcript variants, at least one of which encodes a preproprotein that is proteolytically processed. Processing of this preproprotein generates alpha and beta subunits that heterodimerize to form the mature lysosomal enzyme, which catalyzes the degradation of ceramide into sphingosine and free fatty acid. This enzyme is overexpressed in multiple human cancers and may play a role in cancer progression. Mutations in this gene are associated with the lysosomal storage disorder, Farber lipogranulomatosis, and a neuromuscular disorder, spinal muscular atrophy with progressive myoclonic epilepsy. [provided by RefSeq, Oct 2015]
Associated Conditions (13)
Farber lipogranulomatosis
Inborn genetic diseases
Self-limited epilepsy with centrotemporal spikes
ASAH1-related disorders
Lung cancer
ASAH1-related sphingolipidosis
Arthrogryposis multiplex congenita
Fetal akinesia deformation sequence 1
Spinal muscular atrophy-progressive myoclonic epilepsy syndrome
Abnormality of the nervous system
Uveal melanoma
Ovarian serous cystadenocarcinoma
Abnormality of metabolism/homeostasis
Key Variants
RS1267356970
Conflicting classifications of pathogenicity
Health Risk
RS1354060089
Conflicting classifications of pathogenicity
Farber lipogranulomatosis, Farber lipogranulomatosis
Health Risk
RS138662754
Conflicting classifications of pathogenicity
Farber lipogranulomatosis, Farber lipogranulomatosis
Health Risk
RS138920776
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS141068211
Conflicting classifications of pathogenicity
Farber lipogranulomatosis, Self-limited epilepsy with centrotemporal spikes, Inborn genetic diseases
Health Risk
RS141785977
Conflicting classifications of pathogenicity
Lung cancer, Lung cancer
Health Risk
RS147233112
Conflicting classifications of pathogenicity
Farber lipogranulomatosis, ASAH1-related disorders, Farber lipogranulomatosis
Health Risk
RS147896487
Conflicting classifications of pathogenicity
Self-limited epilepsy with centrotemporal spikes, ASAH1-related sphingolipidosis, Self-limited epilepsy with centrotemporal spikes
Health Risk
RS1588974098
Conflicting classifications of pathogenicity
Farber lipogranulomatosis, Farber lipogranulomatosis
Health Risk
RS1588980220
Conflicting classifications of pathogenicity
Arthrogryposis multiplex congenita, Fetal akinesia deformation sequence 1, Arthrogryposis multiplex congenita
Health Risk
RS1799692515
Conflicting classifications of pathogenicity
Farber lipogranulomatosis, Farber lipogranulomatosis
Health Risk
RS1799735312
Conflicting classifications of pathogenicity
Farber lipogranulomatosis, Farber lipogranulomatosis
Health Risk
All Variants (123)
RSID Category Clinical Significance Conditions
RS1267356970 Health Risk Conflicting classifications of pathogenicity
RS1354060089 Health Risk Conflicting classifications of pathogenicity Farber lipogranulomatosis, Farber lipogranulomatosis
RS138662754 Health Risk Conflicting classifications of pathogenicity Farber lipogranulomatosis, Farber lipogranulomatosis
RS138920776 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS141068211 Health Risk Conflicting classifications of pathogenicity Farber lipogranulomatosis, Self-limited epilepsy with centrotemporal spikes, Inborn genetic diseases
RS141785977 Health Risk Conflicting classifications of pathogenicity Lung cancer, Lung cancer
RS147233112 Health Risk Conflicting classifications of pathogenicity Farber lipogranulomatosis, ASAH1-related disorders, Farber lipogranulomatosis
RS147896487 Health Risk Conflicting classifications of pathogenicity Self-limited epilepsy with centrotemporal spikes, ASAH1-related sphingolipidosis, Self-limited epilepsy with centrotemporal spikes
RS1588974098 Health Risk Conflicting classifications of pathogenicity Farber lipogranulomatosis, Farber lipogranulomatosis
RS1588980220 Health Risk Conflicting classifications of pathogenicity Arthrogryposis multiplex congenita, Fetal akinesia deformation sequence 1, Arthrogryposis multiplex congenita
RS1799692515 Health Risk Conflicting classifications of pathogenicity Farber lipogranulomatosis, Farber lipogranulomatosis
RS1799735312 Health Risk Conflicting classifications of pathogenicity Farber lipogranulomatosis, Farber lipogranulomatosis
RS1800367831 Health Risk Conflicting classifications of pathogenicity Spinal muscular atrophy-progressive myoclonic epilepsy syndrome, Farber lipogranulomatosis, Spinal muscular atrophy-progressive myoclonic epilepsy syndrome
RS189892461 Health Risk Conflicting classifications of pathogenicity Farber lipogranulomatosis, Farber lipogranulomatosis
RS200503438 Health Risk Conflicting classifications of pathogenicity Farber lipogranulomatosis, Farber lipogranulomatosis
RS200758704 Health Risk Conflicting classifications of pathogenicity Arthrogryposis multiplex congenita, Fetal akinesia deformation sequence 1, Farber lipogranulomatosis
RS201735910 Health Risk Conflicting classifications of pathogenicity Farber lipogranulomatosis, Farber lipogranulomatosis
RS371977439 Health Risk Conflicting classifications of pathogenicity Farber lipogranulomatosis, Farber lipogranulomatosis
RS548868946 Health Risk Conflicting classifications of pathogenicity
RS559209309 Health Risk Conflicting classifications of pathogenicity Farber lipogranulomatosis, Farber lipogranulomatosis
RS759177869 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS766257867 Health Risk Conflicting classifications of pathogenicity Spinal muscular atrophy-progressive myoclonic epilepsy syndrome, Spinal muscular atrophy-progressive myoclonic epilepsy syndrome
RS770772909 Health Risk Conflicting classifications of pathogenicity Farber lipogranulomatosis, Farber lipogranulomatosis
RS771021569 Health Risk Conflicting classifications of pathogenicity
RS779888892 Health Risk Conflicting classifications of pathogenicity Spinal muscular atrophy-progressive myoclonic epilepsy syndrome, Spinal muscular atrophy-progressive myoclonic epilepsy syndrome
RS781019071 Health Risk Conflicting classifications of pathogenicity Farber lipogranulomatosis, Farber lipogranulomatosis
RS941670381 Health Risk Conflicting classifications of pathogenicity
RS1019450405 Health Risk Likely pathogenic
RS113532166 Health Risk Likely pathogenic
RS1157855841 Health Risk Likely pathogenic
RS1226438110 Health Risk Likely pathogenic
RS137853594 Health Risk Likely pathogenic Farber lipogranulomatosis, Farber lipogranulomatosis, Farber lipogranulomatosis
RS1411267767 Health Risk Likely pathogenic Farber lipogranulomatosis, Farber lipogranulomatosis
RS1564540455 Health Risk Likely pathogenic Farber lipogranulomatosis, Farber lipogranulomatosis
RS1588973202 Health Risk Likely pathogenic Farber lipogranulomatosis, Spinal muscular atrophy-progressive myoclonic epilepsy syndrome, Farber lipogranulomatosis
RS1588973247 Health Risk Likely pathogenic Farber lipogranulomatosis, Farber lipogranulomatosis
RS1588974267 Health Risk Likely pathogenic Farber lipogranulomatosis, Farber lipogranulomatosis
RS1588974593 Health Risk Likely pathogenic Farber lipogranulomatosis, Farber lipogranulomatosis
RS1588977010 Health Risk Likely pathogenic Farber lipogranulomatosis, Farber lipogranulomatosis
RS1588977181 Health Risk Likely pathogenic Farber lipogranulomatosis, Farber lipogranulomatosis
RS1588978706 Health Risk Likely pathogenic Farber lipogranulomatosis, Farber lipogranulomatosis
RS1588982421 Health Risk Likely pathogenic Farber lipogranulomatosis, Farber lipogranulomatosis
RS1588986195 Health Risk Likely pathogenic Farber lipogranulomatosis, Farber lipogranulomatosis
RS1588999386 Health Risk Likely pathogenic Farber lipogranulomatosis, Farber lipogranulomatosis
RS1588999402 Health Risk Likely pathogenic Farber lipogranulomatosis, Farber lipogranulomatosis
RS1799849914 Health Risk Likely pathogenic
RS2117019094 Health Risk Likely pathogenic
RS2117062166 Health Risk Likely pathogenic
RS2117078394 Health Risk Likely pathogenic Abnormality of the nervous system, Abnormality of the nervous system
RS2537913306 Health Risk Likely pathogenic
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