LAMB3 Chromosome 1

Laminin subunit beta 3
315 variants 315 Health Risk

Upload your DNA to see your personal genotypes for variants in LAMB3.

What This Gene Does
The product encoded by this gene is a laminin that belongs to a family of basement membrane proteins. This protein is a beta subunit laminin, which together with an alpha and a gamma subunit, forms laminin-5. Mutations in this gene cause epidermolysis bullosa junctional Herlitz type, and generalized atrophic benign epidermolysis bullosa, diseases that are characterized by blistering of the skin. Multiple alternatively spliced transcript variants that encode the same protein have been found for this gene. [provided by RefSeq, Jul 2008]
Gene Info
Gene Group
"Laminin subunits|MicroRNA protein coding host genes"
Locus Type
gene with protein product
Location
1q32.2
Ensembl
ENSG00000196878
Associated Conditions (12)
Junctional epidermolysis bullosa gravis of Herlitz
Junctional epidermolysis bullosa
non-Herlitz type
LAMB3-related disorder
Inborn genetic diseases
Amelogenesis imperfecta type 1A
Uterine corpus endometrial carcinoma
Abnormality of the skin
Epidermolysis bullosa
Amelogenesis imperfecta
Epidermolysis bullosa simplex 1A
generalized severe
Key Variants
RS1007125449
Conflicting classifications of pathogenicity
Junctional epidermolysis bullosa gravis of Herlitz, Junctional epidermolysis bullosa, non-Herlitz type
Health Risk
RS1033335294
Conflicting classifications of pathogenicity
Health Risk
RS113745536
Conflicting classifications of pathogenicity
Junctional epidermolysis bullosa, LAMB3-related disorder, Junctional epidermolysis bullosa
Health Risk
RS114274965
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS114404740
Conflicting classifications of pathogenicity
Junctional epidermolysis bullosa, Junctional epidermolysis bullosa
Health Risk
RS114875539
Conflicting classifications of pathogenicity
Junctional epidermolysis bullosa gravis of Herlitz, Junctional epidermolysis bullosa, non-Herlitz type
Health Risk
RS115431256
Conflicting classifications of pathogenicity
Junctional epidermolysis bullosa, Junctional epidermolysis bullosa
Health Risk
RS116124880
Conflicting classifications of pathogenicity
Junctional epidermolysis bullosa, Junctional epidermolysis bullosa
Health Risk
RS116218572
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS12091253
Conflicting classifications of pathogenicity
LAMB3-related disorder, Inborn genetic diseases, LAMB3-related disorder
Health Risk
RS121912486
Conflicting classifications of pathogenicity
Junctional epidermolysis bullosa, non-Herlitz type, Junctional epidermolysis bullosa gravis of Herlitz
Health Risk
RS138710333
Conflicting classifications of pathogenicity
Junctional epidermolysis bullosa, Junctional epidermolysis bullosa
Health Risk
All Variants (315)
RSID Category Clinical Significance Conditions
RS1666731161 Health Risk Pathogenic
RS1666824711 Health Risk Pathogenic
RS1666944608 Health Risk Pathogenic
RS200672750 Health Risk Pathogenic
RS201551805 Health Risk Pathogenic Junctional epidermolysis bullosa gravis of Herlitz, Junctional epidermolysis bullosa, non-Herlitz type
RS2076550971 Health Risk Pathogenic
RS2102403618 Health Risk Pathogenic Junctional epidermolysis bullosa, non-Herlitz type, Epidermolysis bullosa
RS2102405073 Health Risk Pathogenic
RS2102405986 Health Risk Pathogenic
RS2102406610 Health Risk Pathogenic
RS2102406831 Health Risk Pathogenic
RS2102413026 Health Risk Pathogenic
RS2102416503 Health Risk Pathogenic
RS2102420104 Health Risk Pathogenic
RS2102420131 Health Risk Pathogenic
RS2102420949 Health Risk Pathogenic
RS2102424137 Health Risk Pathogenic
RS2102424525 Health Risk Pathogenic Abnormality of the skin, Abnormality of the skin
RS2102430895 Health Risk Pathogenic
RS2102434789 Health Risk Pathogenic
RS2102438416 Health Risk Pathogenic
RS2102444886 Health Risk Pathogenic
RS2102446289 Health Risk Pathogenic
RS2464737467 Health Risk Pathogenic Amelogenesis imperfecta, Amelogenesis imperfecta
RS2464752818 Health Risk Pathogenic Amelogenesis imperfecta type 1A, Junctional epidermolysis bullosa gravis of Herlitz, Junctional epidermolysis bullosa
RS2464753233 Health Risk Pathogenic
RS2464763566 Health Risk Pathogenic
RS2464764722 Health Risk Pathogenic
RS2464785989 Health Risk Pathogenic
RS2464791133 Health Risk Pathogenic
RS2464796651 Health Risk Pathogenic
RS2464797223 Health Risk Pathogenic Junctional epidermolysis bullosa, Junctional epidermolysis bullosa
RS2464813722 Health Risk Pathogenic
RS2464815344 Health Risk Pathogenic
RS2464818105 Health Risk Pathogenic
RS2464820348 Health Risk Pathogenic
RS2464826363 Health Risk Pathogenic
RS2464832578 Health Risk Pathogenic
RS2464832936 Health Risk Pathogenic
RS2464833004 Health Risk Pathogenic
RS2464838281 Health Risk Pathogenic
RS2464838549 Health Risk Pathogenic
RS2464855082 Health Risk Pathogenic
RS2464855898 Health Risk Pathogenic
RS2464866736 Health Risk Pathogenic
RS2464871425 Health Risk Pathogenic
RS2464880681 Health Risk Pathogenic
RS2464894271 Health Risk Pathogenic
RS2464894707 Health Risk Pathogenic
RS2464899127 Health Risk Pathogenic
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