DST Chromosome 6

Dystonin
210 variants 210 Health Risk

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What This Gene Does
This gene encodes a member of the plakin protein family of adhesion junction plaque proteins. Multiple alternatively spliced transcript variants encoding distinct isoforms have been found for this gene, but the full-length nature of some variants has not been defined. It has been reported that some isoforms are expressed in neural and muscle tissue, anchoring neural intermediate filaments to the actin cytoskeleton, and some isoforms are expressed in epithelial tissue, anchoring keratin-containing intermediate filaments to hemidesmosomes. Consistent with the expression, mice defective for this gene show skin blistering and neurodegeneration. [provided by RefSeq, Mar 2010]
Gene Info
Gene Group
"EF-hand domain containing|Plakins|Spectrin repeat containing"
Locus Type
gene with protein product
Location
6p12.1
Ensembl
ENSG00000151914
Associated Conditions (14)
Autism spectrum disorder
Epidermolysis bullosa simplex 3
localized or generalized intermediate
with BP230 deficiency
Hereditary sensory and autonomic neuropathy type 6
Inborn genetic diseases
DST-related disorder
Multiple sclerosis
Familial cancer of breast
Distal spinal muscular atrophy
Congenital contracture
Cardiomyopathy
Hypotonia
Global developmental delay
Key Variants
RS1824238311
association
Autism spectrum disorder, Autism spectrum disorder
Health Risk
RS1020828510
Conflicting classifications of pathogenicity
Epidermolysis bullosa simplex 3, localized or generalized intermediate, with BP230 deficiency
Health Risk
RS112473525
Conflicting classifications of pathogenicity
Hereditary sensory and autonomic neuropathy type 6, Epidermolysis bullosa simplex 3, localized or generalized intermediate
Health Risk
RS112635185
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS116774070
Conflicting classifications of pathogenicity
Epidermolysis bullosa simplex 3, localized or generalized intermediate, with BP230 deficiency
Health Risk
RS1213338072
Conflicting classifications of pathogenicity
Hereditary sensory and autonomic neuropathy type 6, Epidermolysis bullosa simplex 3, localized or generalized intermediate
Health Risk
RS138185589
Conflicting classifications of pathogenicity
Hereditary sensory and autonomic neuropathy type 6, Epidermolysis bullosa simplex 3, localized or generalized intermediate
Health Risk
RS138553142
Conflicting classifications of pathogenicity
Hereditary sensory and autonomic neuropathy type 6, Epidermolysis bullosa simplex 3, localized or generalized intermediate
Health Risk
RS141523606
Conflicting classifications of pathogenicity
Hereditary sensory and autonomic neuropathy type 6, Epidermolysis bullosa simplex 3, localized or generalized intermediate
Health Risk
RS142650835
Conflicting classifications of pathogenicity
Hereditary sensory and autonomic neuropathy type 6, Epidermolysis bullosa simplex 3, localized or generalized intermediate
Health Risk
RS143101723
Conflicting classifications of pathogenicity
Hereditary sensory and autonomic neuropathy type 6, Epidermolysis bullosa simplex 3, localized or generalized intermediate
Health Risk
RS143924906
Conflicting classifications of pathogenicity
Epidermolysis bullosa simplex 3, localized or generalized intermediate, with BP230 deficiency
Health Risk
All Variants (210)
RSID Category Clinical Significance Conditions
RS766657292 Health Risk Conflicting classifications of pathogenicity Epidermolysis bullosa simplex 3, localized or generalized intermediate, with BP230 deficiency
RS767292450 Health Risk Conflicting classifications of pathogenicity Epidermolysis bullosa simplex 3, localized or generalized intermediate, with BP230 deficiency
RS773495985 Health Risk Conflicting classifications of pathogenicity Epidermolysis bullosa simplex 3, localized or generalized intermediate, with BP230 deficiency
RS775912185 Health Risk Conflicting classifications of pathogenicity Epidermolysis bullosa simplex 3, localized or generalized intermediate, with BP230 deficiency
RS777558951 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Hereditary sensory and autonomic neuropathy type 6, Epidermolysis bullosa simplex 3
RS779271284 Health Risk Conflicting classifications of pathogenicity Epidermolysis bullosa simplex 3, localized or generalized intermediate, with BP230 deficiency
RS780009389 Health Risk Conflicting classifications of pathogenicity Hereditary sensory and autonomic neuropathy type 6, Epidermolysis bullosa simplex 3, localized or generalized intermediate
RS780386919 Health Risk Conflicting classifications of pathogenicity Epidermolysis bullosa simplex 3, localized or generalized intermediate, with BP230 deficiency
RS79728438 Health Risk Conflicting classifications of pathogenicity Hereditary sensory and autonomic neuropathy type 6, Epidermolysis bullosa simplex 3, localized or generalized intermediate
RS904996327 Health Risk Conflicting classifications of pathogenicity Hereditary sensory and autonomic neuropathy type 6, Epidermolysis bullosa simplex 3, localized or generalized intermediate
RS994026153 Health Risk Conflicting classifications of pathogenicity Hereditary sensory and autonomic neuropathy type 6, Epidermolysis bullosa simplex 3, localized or generalized intermediate
RS1242078669 Health Risk Likely pathogenic Hereditary sensory and autonomic neuropathy type 6, Hereditary sensory and autonomic neuropathy type 6
RS1310802903 Health Risk Likely pathogenic
RS1312420010 Health Risk Likely pathogenic Epidermolysis bullosa simplex 3, localized or generalized intermediate, with BP230 deficiency
RS1341890249 Health Risk Likely pathogenic
RS1404977690 Health Risk Likely pathogenic Hereditary sensory and autonomic neuropathy type 6, Epidermolysis bullosa simplex 3, localized or generalized intermediate
RS1454639285 Health Risk Likely pathogenic Hereditary sensory and autonomic neuropathy type 6, Epidermolysis bullosa simplex 3, localized or generalized intermediate
RS1587154269 Health Risk Likely pathogenic Hereditary sensory and autonomic neuropathy type 6, Epidermolysis bullosa simplex 3, localized or generalized intermediate
RS200803122 Health Risk Likely pathogenic Hereditary sensory and autonomic neuropathy type 6, Epidermolysis bullosa simplex 3, localized or generalized intermediate
RS2094441686 Health Risk Likely pathogenic Epidermolysis bullosa simplex 3, localized or generalized intermediate, with BP230 deficiency
RS2096858510 Health Risk Likely pathogenic Hereditary sensory and autonomic neuropathy type 6, Epidermolysis bullosa simplex 3, localized or generalized intermediate
RS2152370482 Health Risk Likely pathogenic Epidermolysis bullosa simplex 3, localized or generalized intermediate, with BP230 deficiency
RS2152394710 Health Risk Likely pathogenic Hereditary sensory and autonomic neuropathy type 6, Epidermolysis bullosa simplex 3, localized or generalized intermediate
RS2152422891 Health Risk Likely pathogenic Hereditary sensory and autonomic neuropathy type 6, Epidermolysis bullosa simplex 3, localized or generalized intermediate
RS2152427474 Health Risk Likely pathogenic Epidermolysis bullosa simplex 3, localized or generalized intermediate, with BP230 deficiency
RS2152440123 Health Risk Likely pathogenic Epidermolysis bullosa simplex 3, localized or generalized intermediate, with BP230 deficiency
RS2152506082 Health Risk Likely pathogenic Epidermolysis bullosa simplex 3, localized or generalized intermediate, with BP230 deficiency
RS2152697802 Health Risk Likely pathogenic Hereditary sensory and autonomic neuropathy type 6, Epidermolysis bullosa simplex 3, localized or generalized intermediate
RS2533409853 Health Risk Likely pathogenic Hereditary sensory and autonomic neuropathy type 6, Epidermolysis bullosa simplex 3, localized or generalized intermediate
RS2533686042 Health Risk Likely pathogenic Epidermolysis bullosa simplex 3, localized or generalized intermediate, with BP230 deficiency
RS2534159000 Health Risk Likely pathogenic Hereditary sensory and autonomic neuropathy type 6, Epidermolysis bullosa simplex 3, localized or generalized intermediate
RS2534263051 Health Risk Likely pathogenic Hereditary sensory and autonomic neuropathy type 6, Epidermolysis bullosa simplex 3, localized or generalized intermediate
RS2534371010 Health Risk Likely pathogenic Hereditary sensory and autonomic neuropathy type 6, Epidermolysis bullosa simplex 3, localized or generalized intermediate
RS2534813697 Health Risk Likely pathogenic Inborn genetic diseases, Inborn genetic diseases
RS2536399953 Health Risk Likely pathogenic Hereditary sensory and autonomic neuropathy type 6, Hereditary sensory and autonomic neuropathy type 6
RS2536948872 Health Risk Likely pathogenic Epidermolysis bullosa simplex 3, localized or generalized intermediate, with BP230 deficiency
RS2537162620 Health Risk Likely pathogenic Hereditary sensory and autonomic neuropathy type 6, Epidermolysis bullosa simplex 3, localized or generalized intermediate
RS748746313 Health Risk Likely pathogenic Hereditary sensory and autonomic neuropathy type 6, Epidermolysis bullosa simplex 3, localized or generalized intermediate
RS748845919 Health Risk Likely pathogenic
RS757600961 Health Risk Likely pathogenic Hereditary sensory and autonomic neuropathy type 6, Epidermolysis bullosa simplex 3, localized or generalized intermediate
RS779625484 Health Risk Likely pathogenic Hereditary sensory and autonomic neuropathy type 6, Hereditary sensory and autonomic neuropathy type 6
RS1057524203 Health Risk Pathogenic
RS1188417345 Health Risk Pathogenic Hereditary sensory and autonomic neuropathy type 6, Epidermolysis bullosa simplex 3, localized or generalized intermediate
RS1198127456 Health Risk Pathogenic Epidermolysis bullosa simplex 3, localized or generalized intermediate, with BP230 deficiency
RS1247419225 Health Risk Pathogenic Epidermolysis bullosa simplex 3, localized or generalized intermediate, with BP230 deficiency
RS1270417432 Health Risk Pathogenic Hereditary sensory and autonomic neuropathy type 6, Epidermolysis bullosa simplex 3, localized or generalized intermediate
RS1277472105 Health Risk Pathogenic Hereditary sensory and autonomic neuropathy type 6, Epidermolysis bullosa simplex 3, localized or generalized intermediate
RS1284559589 Health Risk Pathogenic Epidermolysis bullosa simplex 3, localized or generalized intermediate, with BP230 deficiency
RS1376812152 Health Risk Pathogenic Hereditary sensory and autonomic neuropathy type 6, Epidermolysis bullosa simplex 3, localized or generalized intermediate
RS1392325549 Health Risk Pathogenic Hereditary sensory and autonomic neuropathy type 6, Epidermolysis bullosa simplex 3, localized or generalized intermediate
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