LAMC3 Chromosome 9

Laminin subunit gamma 3
155 variants 155 Health Risk

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What This Gene Does
Laminins, a family of extracellular matrix glycoproteins, are the major noncollagenous constituent of basement membranes. They have been implicated in a wide variety of biological processes including cell adhesion, differentiation, migration, signaling, neurite outgrowth and metastasis. Laminins are composed of 3 non identical chains: laminin alpha, beta and gamma (formerly A, B1, and B2, respectively) and they form a cruciform structure consisting of 3 short arms, each formed by a different chain, and a long arm composed of all 3 chains. Each laminin chain is a multidomain protein encoded by a distinct gene. Several isoforms of each chain have been described. Different alpha, beta and gamma chain isomers combine to give rise to different heterotrimeric laminin isoforms which are designated by Arabic numerals in the order of their discovery, i.e. alpha1beta1gamma1 heterotrimer is laminin 1. The biological functions of the different chains and trimer molecules are largely unknown, but some of the chains have been shown to differ with respect to their tissue distribution, presumably reflecting diverse functions in vivo. This gene encodes the gamma chain isoform laminin, gamma 3. The gamma 3 chain is most similar to the gamma 1 chain, and contains all the 6 domains expected of the gamma chain. It is a component of laminin 12. The gamma 3 chain is broadly expressed in skin, heart, lung, and the reproductive tracts. In skin, it is seen within the basement membrane of the dermal-epidermal junction at points of nerve penetration. Gamma 3 is also a prominent element of the apical surface of ciliated epithelial cells of lung, oviduct, epididymis, ductus deferens, and seminiferous tubules. The distribution of gamma 3-containing laminins along ciliated epithelial surfaces suggests that the apical laminins are important in the morphogenesis and structural stability of the ciliated processes of these cells. [provided by RefSeq, Aug 2011]
Gene Info
Gene Group
Laminin subunits
Locus Type
gene with protein product
Location
9q34.12
Ensembl
ENSG00000050555
Associated Conditions (15)
Inborn genetic diseases
Occipital pachygyria and polymicrogyria
LAMC3-related disorder
Clear cell carcinoma of kidney
Malignant tumor of esophagus
Melanoma
Ovarian cancer
Left ventricular noncompaction
Colon adenocarcinoma
Hepatocellular carcinoma
See cases
Intellectual disability
Thyroid cancer
nonmedullary
1
Key Variants
RS1055925150
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS1057207177
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS1057520165
Conflicting classifications of pathogenicity
Occipital pachygyria and polymicrogyria, Occipital pachygyria and polymicrogyria
Health Risk
RS113354770
Conflicting classifications of pathogenicity
Occipital pachygyria and polymicrogyria, Inborn genetic diseases, Occipital pachygyria and polymicrogyria
Health Risk
RS113443891
Conflicting classifications of pathogenicity
Occipital pachygyria and polymicrogyria, Inborn genetic diseases, LAMC3-related disorder
Health Risk
RS113785045
Conflicting classifications of pathogenicity
Inborn genetic diseases, LAMC3-related disorder, Inborn genetic diseases
Health Risk
RS1238856355
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS1377008496
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS137883250
Conflicting classifications of pathogenicity
Health Risk
RS138481447
Conflicting classifications of pathogenicity
Occipital pachygyria and polymicrogyria, Inborn genetic diseases, LAMC3-related disorder
Health Risk
RS139905505
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS140325029
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
All Variants (155)
RSID Category Clinical Significance Conditions
RS371411184 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS373660982 Health Risk Conflicting classifications of pathogenicity Thyroid cancer, nonmedullary, 1
RS375139277 Health Risk Conflicting classifications of pathogenicity
RS375541717 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS375971925 Health Risk Conflicting classifications of pathogenicity
RS555619019 Health Risk Conflicting classifications of pathogenicity
RS563444562 Health Risk Conflicting classifications of pathogenicity
RS749496192 Health Risk Conflicting classifications of pathogenicity Intellectual disability, Inborn genetic diseases, Occipital pachygyria and polymicrogyria
RS754122699 Health Risk Conflicting classifications of pathogenicity
RS756683242 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS765657893 Health Risk Conflicting classifications of pathogenicity
RS769198717 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS770428385 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS771657438 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS774738544 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS778920875 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS900991986 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS927249367 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS1170064033 Health Risk Likely pathogenic Occipital pachygyria and polymicrogyria, Occipital pachygyria and polymicrogyria
RS1285969385 Health Risk Likely pathogenic
RS1402701697 Health Risk Likely pathogenic Occipital pachygyria and polymicrogyria, Occipital pachygyria and polymicrogyria
RS1439284027 Health Risk Likely pathogenic Occipital pachygyria and polymicrogyria, Occipital pachygyria and polymicrogyria
RS1554789398 Health Risk Likely pathogenic
RS1564368059 Health Risk Likely pathogenic
RS1564371083 Health Risk Likely pathogenic
RS1588171883 Health Risk Likely pathogenic
RS1829945601 Health Risk Likely pathogenic
RS1833833523 Health Risk Likely pathogenic LAMC3-related disorder, LAMC3-related disorder
RS2133322852 Health Risk Likely pathogenic Occipital pachygyria and polymicrogyria, Occipital pachygyria and polymicrogyria
RS2490680513 Health Risk Likely pathogenic
RS2490714618 Health Risk Likely pathogenic
RS2490715564 Health Risk Likely pathogenic Occipital pachygyria and polymicrogyria, Occipital pachygyria and polymicrogyria
RS2490716828 Health Risk Likely pathogenic
RS2538300291 Health Risk Likely pathogenic
RS2538301349 Health Risk Likely pathogenic
RS2538314828 Health Risk Likely pathogenic
RS746890847 Health Risk Likely pathogenic
RS756587349 Health Risk Likely pathogenic
RS761516738 Health Risk Likely pathogenic Occipital pachygyria and polymicrogyria, Occipital pachygyria and polymicrogyria
RS765835831 Health Risk Likely pathogenic
RS768710385 Health Risk Likely pathogenic
RS775851709 Health Risk Likely pathogenic Occipital pachygyria and polymicrogyria, Occipital pachygyria and polymicrogyria
RS778619122 Health Risk Likely pathogenic
RS781432366 Health Risk Likely pathogenic Occipital pachygyria and polymicrogyria, Occipital pachygyria and polymicrogyria
RS927587368 Health Risk Likely pathogenic
RS1011715171 Health Risk Pathogenic
RS1030229080 Health Risk Pathogenic
RS1219639490 Health Risk Pathogenic
RS1288962949 Health Risk Pathogenic
RS1334057595 Health Risk Pathogenic
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