LTBP2 Chromosome 14

Latent transforming growth factor beta binding protein 2
155 variants 155 Health Risk

Upload your DNA to see your personal genotypes for variants in LTBP2.

What This Gene Does
The protein encoded by this gene belongs to the family of latent transforming growth factor (TGF)-beta binding proteins (LTBP), which are extracellular matrix proteins with multi-domain structure. This protein is the largest member of the LTBP family possessing unique regions and with most similarity to the fibrillins. It has thus been suggested that it may have multiple functions: as a member of the TGF-beta latent complex, as a structural component of microfibrils, and a role in cell adhesion. [provided by RefSeq, Jul 2008]
Gene Info
Gene Group
Latent transforming growth factor beta binding proteins
Locus Type
gene with protein product
Location
14q24.3
Ensembl
ENSG00000119681
Associated Conditions (22)
Glaucoma 3
primary congenital
D
Weill-Marchesani syndrome
Weill-Marchesani syndrome 3
Microspherophakia and/or megalocornea
with ectopia lentis and with or without secondary glaucoma
LTBP2-related disorder
Inborn genetic diseases
Pseudoexfoliation glaucoma
Primary open angle glaucoma
primary infantile
B
Ovarian serous cystadenocarcinoma
Uterine carcinosarcoma
Thymoma
Familial cancer of breast
Microspherophakia
Glaucoma 3A
Marfan syndrome
+2 more conditions
Key Variants
RS1004486722
Conflicting classifications of pathogenicity
Glaucoma 3, primary congenital, D
Health Risk
RS111342797
Conflicting classifications of pathogenicity
Weill-Marchesani syndrome, Glaucoma 3, primary congenital
Health Risk
RS113219139
Conflicting classifications of pathogenicity
Weill-Marchesani syndrome, Glaucoma 3, primary congenital
Health Risk
RS117800773
Conflicting classifications of pathogenicity
Glaucoma 3, primary congenital, D
Health Risk
RS1194291909
Conflicting classifications of pathogenicity
Weill-Marchesani syndrome, Glaucoma 3, primary congenital
Health Risk
RS1206472219
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS137854861
Conflicting classifications of pathogenicity
Pseudoexfoliation glaucoma, Weill-Marchesani syndrome, Weill-Marchesani syndrome 3
Health Risk
RS137854863
Conflicting classifications of pathogenicity
Primary open angle glaucoma, Microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucoma
Health Risk
RS137854886
Conflicting classifications of pathogenicity
Pseudoexfoliation glaucoma, Weill-Marchesani syndrome, Glaucoma 3
Health Risk
RS137871407
Conflicting classifications of pathogenicity
Glaucoma 3, primary congenital, D
Health Risk
RS138194436
Conflicting classifications of pathogenicity
Weill-Marchesani syndrome, Glaucoma 3, primary congenital
Health Risk
RS139018077
Conflicting classifications of pathogenicity
Weill-Marchesani syndrome, Glaucoma 3, primary congenital
Health Risk
All Variants (155)
RSID Category Clinical Significance Conditions
RS1327636983 Health Risk Likely pathogenic Weill-Marchesani syndrome 3, Glaucoma 3, primary infantile
RS137854858 Health Risk Likely pathogenic Primary open angle glaucoma, Primary open angle glaucoma
RS1566660365 Health Risk Likely pathogenic Glaucoma 3, primary congenital, D
RS201872469 Health Risk Likely pathogenic
RS2087144643 Health Risk Likely pathogenic
RS2139689656 Health Risk Likely pathogenic
RS2139715414 Health Risk Likely pathogenic Microspherophakia, Microspherophakia
RS2139815316 Health Risk Likely pathogenic
RS2506127645 Health Risk Likely pathogenic LTBP2-related disorder, LTBP2-related disorder
RS2506144425 Health Risk Likely pathogenic
RS2506152687 Health Risk Likely pathogenic
RS387907175 Health Risk Likely pathogenic Microspherophakia, Microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucoma
RS756727211 Health Risk Likely pathogenic
RS773910322 Health Risk Likely pathogenic Microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucoma, Microspherophakia and/or megalocornea
RS774139166 Health Risk Likely pathogenic Glaucoma 3, primary congenital, D
RS778560568 Health Risk Likely pathogenic
RS1160610120 Health Risk Pathogenic
RS1216378691 Health Risk Pathogenic
RS121918355 Health Risk Pathogenic Glaucoma 3, primary congenital, D
RS121918356 Health Risk Pathogenic Glaucoma 3, primary congenital, D
RS1296682446 Health Risk Pathogenic
RS1299329919 Health Risk Pathogenic
RS137854855 Health Risk Pathogenic Marfan syndrome, Marfan syndrome
RS137854856 Health Risk Pathogenic Weill-Marchesani syndrome 3, Weill-Marchesani syndrome 1, Weill-Marchesani syndrome 3
RS137854895 Health Risk Pathogenic Glaucoma 3, primary congenital, D
RS1388677499 Health Risk Pathogenic
RS1420141860 Health Risk Pathogenic
RS1454530658 Health Risk Pathogenic
RS1467675240 Health Risk Pathogenic
RS1566628109 Health Risk Pathogenic Microspherophakia, Microspherophakia
RS1566634475 Health Risk Pathogenic Glaucoma 3, primary congenital, D
RS1566635134 Health Risk Pathogenic Glaucoma 3, primary congenital, D
RS1566636728 Health Risk Pathogenic Microspherophakia, Microspherophakia
RS2139693289 Health Risk Pathogenic
RS2139718507 Health Risk Pathogenic
RS2139788041 Health Risk Pathogenic
RS2139815717 Health Risk Pathogenic
RS2506128996 Health Risk Pathogenic
RS2506133762 Health Risk Pathogenic Microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucoma, Microspherophakia and/or megalocornea
RS2506134863 Health Risk Pathogenic
RS2506136232 Health Risk Pathogenic
RS2506136529 Health Risk Pathogenic
RS2506148934 Health Risk Pathogenic
RS35915872 Health Risk Pathogenic
RS387907174 Health Risk Pathogenic Microspherophakia, Microspherophakia
RS747161431 Health Risk Pathogenic
RS760404952 Health Risk Pathogenic
RS762228239 Health Risk Pathogenic
RS766444609 Health Risk Pathogenic
RS768947464 Health Risk Pathogenic
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