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COL11A1 gene

Known as: COL11A1, collagen type XI alpha 1, COLLAGEN, TYPE XI, ALPHA-1 
This gene is involved in the maintenance of cartilage.
National Institutes of Health

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COL11A1 wt Allele
COL15A1 geneCell AdhesionCell MovementCollagen Alpha-1 (XI) Chain

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
Application of high‐resolution array platform for genome‐wide copy number variation analysis in patients with nonsyndromic cleft lip and palate
Although more than 14 loci may be involved in the development of nonsyndromic cleft lip and palate (NSCLP), the etiology has not… 
2017
2017
A genetic variant in COL11A1 is functionally associated with lumbar disc herniation in Chinese population
This study aimed to explore whether the genetic variant of COL11A1 is functionally associated with the development of lumbar disc… 
2017
2017
Screening key genes and miRNAs in early-stage colon adenocarcinoma by RNA-sequencing
Colon adenocarcinoma is the third leading cause of cancer-related deaths across the world, developing novel and non-invasive… 
2017
2017
Sesamin encouraging effects on chondrogenic differentiation of human amniotic fluid-derived mesenchymal stem cells.
Review
2015
Review
2015
Genetic associations in PLEKHA7 and COL11A1 with primary angle closure glaucoma: a meta‐analysis
Single nucleotide polymorphisms (SNPs) rs11024102 in PLEKHA7 and rs3753841 in COL11A1 were identified to be associated with… 
Review
2013
Review
2013
An Extensive Replication Study on Three New Susceptibility Loci of Primary Angle Closure Glaucoma in Han Chinese: Jiangsu Eye Study
Genome-wide association study (GWAS) analysis identified three new susceptibility loci for PACG. In this study, we aimed to… 
2003
2003
Posterior chorioretinal atrophy and vitreous phenotype in a family with Stickler syndrome from a mutation in the COL2A1 gene.
Highly Cited
2001
Highly Cited
2001
Auditory dysfunction in Stickler syndrome.
OBJECTIVES To characterize the natural history and possible mechanisms of hearing loss in Stickler syndrome (OMIM 108300; or… 
2000
2000
Audiovestibular phenotype associated with a COL11A1 mutation in Marshall syndrome.
BACKGROUND Marshall syndrome is a dominant disorder characterized by craniofacial and skeletal abnormalities, sensorineural… 
1995
1995
Structural and Functional Analysis of the Promoter of the Human 1(XI) Collagen Gene (*)
In order to eventually elucidate the mechanisms regulating α1(XI) collagen expression in cartilaginous and non-cartilaginous… 
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