COL11A1 collagen type XI alpha 1 chain [Homo sapiens (human)] - Gene

Summary

Official Symbol: COL11A1provided by HGNC
Official Full Name: collagen type XI alpha 1 chainprovided by HGNC
Primary source: HGNC:HGNC:2186
See related: Ensembl:ENSG00000060718 MIM:120280; AllianceGenome:HGNC:2186
Gene type: protein coding
RefSeq status: REVIEWED
Organism: Homo sapiens
Lineage: Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as: STL2; COLL6; CO11A1; DFNA37
Summary: This gene encodes one of the two alpha chains of type XI collagen, a minor fibrillar collagen. Type XI collagen is a heterotrimer but the third alpha chain is a post-translationally modified alpha 1 type II chain. Mutations in this gene are associated with type II Stickler syndrome and with Marshall syndrome. A single-nucleotide polymorphism in this gene is also associated with susceptibility to lumbar disc herniation. Multiple transcript variants have been identified for this gene. [provided by RefSeq, Nov 2009]
Expression: Biased expression in placenta (RPKM 6.4), gall bladder (RPKM 1.9) and 4 other tissues See more
Orthologs: mouse all
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Genomic context

Location:: 1p21.1

Exon count:: 73

Annotation release	Status	Assembly	Chr	Location
RS_2024_08	current	GRCh38.p14 (GCF_000001405.40)	1	NC_000001.11 (102876473..103108522, complement)
RS_2024_08	current	T2T-CHM13v2.0 (GCF_009914755.1)	1	NC_060925.1 (102725394..102957399, complement)
RS_2024_09	previous assembly	GRCh37.p13 (GCF_000001405.25)	1	NC_000001.10 (103342029..103574078, complement)

Chromosome 1 - NC_000001.11 Genomic Context describing neighboring genes

Genomic regions, transcripts, and products

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Go to reference sequence details

Genomic Sequence:

Go to nucleotide: Graphics FASTA GenBank

Expression

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See details

Project title: Tissue-specific circular RNA induction during human fetal development
Description: 35 human fetal samples from 6 tissues (3 - 7 replicates per tissue) collected between 10 and 20 weeks gestational time were sequenced using Illumina TruSeq Stranded Total RNA
BioProject: PRJNA270632
Publication: PMID 26076956
Analysis date: Mon Apr 2 22:54:59 2018

Bibliography

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GeneRIFs: Gene References Into Functions

What's a GeneRIF?

Microphthalmia and congenital cataract in two patients with Stickler syndrome type II: a case report.
Title: Microphthalmia and congenital cataract in two patients with Stickler syndrome type II: a case report.
Analysis of cancer-associated fibroblasts related genes identifies COL11A1 associated with lung adenocarcinoma prognosis.
Title: Analysis of cancer-associated fibroblasts related genes identifies COL11A1 associated with lung adenocarcinoma prognosis.
Association of genetic variation in COL11A1 with adolescent idiopathic scoliosis.
Title: Association of genetic variation in COL11A1 with adolescent idiopathic scoliosis.
Circular circRANGAP1 Contributes to Non-small Cell Lung Cancer Progression by Increasing COL11A1 Expression Through Sponging miR-653-5p.
Title: Circular circRANGAP1 Contributes to Non-small Cell Lung Cancer Progression by Increasing COL11A1 Expression Through Sponging miR-653-5p.
Collagen 1A1 (COL1A1) and Collagen11A1(COL11A1) as diagnostic biomarkers in Breast, colorectal and gastric cancers.
Title: Collagen 1A1 (COL1A1) and Collagen11A1(COL11A1) as diagnostic biomarkers in Breast, colorectal and gastric cancers.
Association Between COL5a1, COL11a1, and COL11a2 Gene Variations and Rotator Cuff Tendinopathy in Young Athletes.
Title: Association Between COL5a1, COL11a1, and COL11a2 Gene Variations and Rotator Cuff Tendinopathy in Young Athletes.
[COL11A1 regulates PI3K/Akt/GSK-3beta pathway and promotes human lung adenocarcinoma primary cell migration and invasion].
Title: [COL11A1 regulates PI3K/Akt/GSK-3β pathway and promotes human lung adenocarcinoma primary cell migration and invasion].
COL11A1-driven positive feedback loop modulates fibroblast transformation and activates pancreatic cancer progression.
Title: COL11A1-driven positive feedback loop modulates fibroblast transformation and activates pancreatic cancer progression.
Genetic associations in CHAT and COL11A1 with primary angle-closure glaucoma susceptibility: A systematic review and meta-analysis.
Title: Genetic associations in CHAT and COL11A1 with primary angle-closure glaucoma susceptibility: A systematic review and meta-analysis.
The Association of Variants within Types V and XI Collagen Genes with Knee Joint Laxity Measurements.
Title: The Association of Variants within Types V and XI Collagen Genes with Knee Joint Laxity Measurements.

Submit: New GeneRIF Correction See all GeneRIFs (101)

Phenotypes

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Find tests for this gene in the NIH Genetic Testing Registry (GTR)

Review eQTL and phenotype association data in this region using PheGenI

Associated conditions

Description	Tests
Fibrochondrogenesis 1 MedGen: C3278138 OMIM: 228520 GeneReviews: Not available	Compare labs
Hearing loss, autosomal dominant 37 MedGen: C4760307 OMIM: 618533 GeneReviews: Not available	Compare labs
Intervertebral disc disorder MedGen: C0158252 OMIM: 603932 GeneReviews: Not available	Compare labs
Marshall syndrome MedGen: C0265235 OMIM: 154780 GeneReviews: Not available	Compare labs
Stickler syndrome type 2 MedGen: C1858084 OMIM: 604841 GeneReviews: Stickler Syndrome	Compare labs

Copy number response

Description
Copy number response Triplosensitivity No evidence available (Last evaluated 2011-10-19) ClinGen Genome Curation Page Haploinsufficency Little evidence for dosage pathogenicity (Last evaluated 2011-10-19) ClinGen Genome Curation PagePubMed

EBI GWAS Catalog

Description
A genome-wide association study identifies protein quantitative trait loci (pQTLs). EBI GWAS Catalog EBI GWAS CatalogPubMed
Genome-wide association analyses identify three new susceptibility loci for primary angle closure glaucoma. EBI GWAS Catalog EBI GWAS CatalogPubMed
Genome-wide meta-analysis identifies 56 bone mineral density loci and reveals 14 loci associated with risk of fracture. EBI GWAS Catalog EBI GWAS CatalogPubMed

Variation

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See variants in ClinVar

See studies and variants in dbVar

See Variation Viewer (GRCh37.p13)

See Variation Viewer (GRCh38)

Interactions

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Products	Interactant	Other Gene	Complex	Source	Pubs	Description

General gene information

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Markers

WI-15584 (e-PCR)
- UniSTS:47123

RH98519 (e-PCR)
- UniSTS:90929

SHGC-75227 (e-PCR)
- UniSTS:40016

AL034233 (e-PCR)
- UniSTS:94050

SHGC-75242 (e-PCR)
- UniSTS:26770

Cda1db02 (e-PCR)
- UniSTS:48817

AL033959 (e-PCR)
- UniSTS:93371

SHGC-35204 (e-PCR)
- UniSTS:26060

D1S3215 (e-PCR)
- UniSTS:56272

Gene Ontology Provided by GOA

Function	Evidence Code	Pubs
enables extracellular matrix binding	NAS Non-traceable Author Statement more info	PubMed
enables extracellular matrix structural constituent	NAS Non-traceable Author Statement more info	PubMed
enables extracellular matrix structural constituent conferring tensile strength	IBA Inferred from Biological aspect of Ancestor more info
enables extracellular matrix structural constituent conferring tensile strength	RCA inferred from Reviewed Computational Analysis more info	PubMed
enables heparan sulfate binding	IEA Inferred from Electronic Annotation more info
enables heparin binding	IBA Inferred from Biological aspect of Ancestor more info
enables metal ion binding	IEA Inferred from Electronic Annotation more info
enables protein-macromolecule adaptor activity	NAS Non-traceable Author Statement more info	PubMed

Process	Evidence Code	Pubs
involved_in cartilage condensation	IEA Inferred from Electronic Annotation more info
involved_in chondrocyte development	IEA Inferred from Electronic Annotation more info
involved_in collagen fibril organization	NAS Non-traceable Author Statement more info	PubMed
involved_in detection of mechanical stimulus involved in sensory perception of sound	IMP Inferred from Mutant Phenotype more info	PubMed
involved_in embryonic skeletal system morphogenesis	IEA Inferred from Electronic Annotation more info
involved_in endodermal cell differentiation	IEP Inferred from Expression Pattern more info	PubMed
involved_in extracellular matrix organization	IBA Inferred from Biological aspect of Ancestor more info
involved_in extracellular matrix organization	NAS Non-traceable Author Statement more info	PubMed
involved_in inner ear morphogenesis	IEA Inferred from Electronic Annotation more info
involved_in ossification	IEA Inferred from Electronic Annotation more info
involved_in proteoglycan metabolic process	IEA Inferred from Electronic Annotation more info
involved_in sensory perception of sound	IMP Inferred from Mutant Phenotype more info	PubMed
involved_in tendon development	IEA Inferred from Electronic Annotation more info
involved_in ventricular cardiac muscle tissue morphogenesis	IEA Inferred from Electronic Annotation more info
involved_in visual perception	IMP Inferred from Mutant Phenotype more info	PubMed

Component	Evidence Code	Pubs
part_of collagen type XI trimer	IBA Inferred from Biological aspect of Ancestor more info
part_of collagen type XI trimer	IDA Inferred from Direct Assay more info	PubMed
part_of collagen type XI trimer	NAS Non-traceable Author Statement more info	PubMed
located_in collagen-containing extracellular matrix	HDA more info	PubMed
is_active_in collagen-containing extracellular matrix	IBA Inferred from Biological aspect of Ancestor more info
located_in collagen-containing extracellular matrix	NAS Non-traceable Author Statement more info	PubMed
located_in endoplasmic reticulum lumen	TAS Traceable Author Statement more info
located_in extracellular region	TAS Traceable Author Statement more info
is_active_in extracellular space	IBA Inferred from Biological aspect of Ancestor more info

General protein information

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Preferred Names: collagen alpha-1(XI) chain

Names: collagen XI, alpha-1 polypeptide; collagen, type XI, alpha 1; deafness, autosomal dominant 37

NCBI Reference Sequences (RefSeq)

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RefSeqs maintained independently of Annotated Genomes

These reference sequences exist independently of genome builds. Explain

These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.

Genomic

NG_008033.2 RefSeqGene

Range

4975..237024

Download

GenBank, FASTA, Sequence Viewer (Graphics)

mRNA and Protein(s)

NM_001190709.2 → NP_001177638.1 collagen alpha-1(XI) chain isoform E preproprotein

Status: REVIEWED

Description

Transcript Variant: This variant (E, previously referred to as C) does not utilize either alternate exon 6A or 6B. The encoded isoform (E, previously referred to as C) is shorter than isoform A. There are no publicly available transcripts representing this variant; it is supported by mRNA annotation on DNA accession AF101112.1, protein AAF04724.1, submitted by the authors of PMID:10486316.

Source sequence(s)

AB208844, AC093150, AC099567, BU159588, BX476821, CA448616, J04177

Consensus CDS

CCDS53348.1

Related

ENSP00000302551.6, ENST00000353414.8

Conserved Domains (3) summary

pfam01391
Location:802 → 861

Collagen; Collagen triple helix repeat (20 copies)

smart00210
Location:38 → 229

TSPN; Thrombospondin N-terminal -like domains

pfam01410
Location:1539 → 1765

COLFI; Fibrillar collagen C-terminal domain
NM_001854.4 → NP_001845.3 collagen alpha-1(XI) chain isoform A preproprotein

See identical proteins and their annotated locations for NP_001845.3

Status: REVIEWED

Description

Transcript Variant: This variant (A) utilizes alternate exon 6, designated exon 6A. The encoded isoform (A) has a 39 aa region specified by exon 6A, that differs from the corresponding 51 aa region encoded by exon 6B in isoform B.

Source sequence(s)

AB208844, AC093150, AC099567, BU159588, BX476821, J04177

Consensus CDS

CCDS778.1

UniProtKB/Swiss-Prot

B1ASK7, D3DT73, E9PCU0, P12107, Q14034, Q149N0, Q9UIT4, Q9UIT5, Q9UIT6

Related

ENSP00000359114.3, ENST00000370096.9

Conserved Domains (3) summary

pfam01391
Location:841 → 900

Collagen; Collagen triple helix repeat (20 copies)

smart00210
Location:38 → 229

TSPN; Thrombospondin N-terminal -like domains

pfam01410
Location:1578 → 1804

COLFI; Fibrillar collagen C-terminal domain
NM_080629.3 → NP_542196.2 collagen alpha-1(XI) chain isoform B preproprotein

See identical proteins and their annotated locations for NP_542196.2

Status: REVIEWED

Description

Transcript Variant: This variant (B) utilizes alternate exon 6, designated exon 6B, and encodes the longest isoform (B). There are no publicly available transcripts representing this variant; it is supported by mRNA annotation on DNA accession AF101112.1, protein AAF04726.1, submitted by the authors of PMID:10486316.

Source sequence(s)

AB208844, AC093150, AC099567, BU159588, BX476821, J04177

Related

ENSP00000351163.2, ENST00000358392.6

Conserved Domains (3) summary

pfam01391
Location:853 → 912

Collagen; Collagen triple helix repeat (20 copies)

smart00210
Location:38 → 229

TSPN; Thrombospondin N-terminal -like domains

pfam01410
Location:1590 → 1816

COLFI; Fibrillar collagen C-terminal domain
NM_080630.4 → NP_542197.3 collagen alpha-1(XI) chain isoform C preproprotein

See identical proteins and their annotated locations for NP_542197.3

Status: REVIEWED

Description

Transcript Variant: This variant (C, previously referred to as D) includes alternate exon 6A but lacks two other alternate exons, resulting in the loss of an in-frame segment in the coding region, compared to variant A. The encoded isoform (C, previously referred to as D) is shorter than isoform A.

Source sequence(s)

AC093150, AC099567, BC117697, CA448616

Consensus CDS

CCDS780.2

Related

ENSP00000426533.1, ENST00000512756.5

Conserved Domains (3) summary

pfam01391
Location:725 → 784

Collagen; Collagen triple helix repeat (20 copies)

smart00210
Location:38 → 229

TSPN; Thrombospondin N-terminal -like domains

pfam01410
Location:1462 → 1688

COLFI; Fibrillar collagen C-terminal domain

RNA

NR_134980.2 RNA Sequence

Status: REVIEWED

Description

Transcript Variant: This variant (F) contains an alternate internal exon compared to variant A. This variant is represented as non-coding because the use of the 5'-most expected translational start codon renders the transcript a candidate for nonsense-mediated mRNA decay (NMD).

Source sequence(s)

AB208844, AC093150, AC099567, BC117697, CA448616