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COL5A1 collagen type V alpha 1 chain [ Homo sapiens (human) ]

Gene ID: 1289, updated on 3-Apr-2024

Summary

Official Symbol
COL5A1provided by HGNC
Official Full Name
collagen type V alpha 1 chainprovided by HGNC
Primary source
HGNC:HGNC:2209
See related
Ensembl:ENSG00000130635 MIM:120215; AllianceGenome:HGNC:2209
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
EDSC; FMDMF; EDSCL1
Summary
This gene encodes an alpha chain for one of the low abundance fibrillar collagens. Fibrillar collagen molecules are trimers that can be composed of one or more types of alpha chains. Type V collagen is found in tissues containing type I collagen and appears to regulate the assembly of heterotypic fibers composed of both type I and type V collagen. This gene product is closely related to type XI collagen and it is possible that the collagen chains of types V and XI constitute a single collagen type with tissue-specific chain combinations. The encoded procollagen protein occurs commonly as the heterotrimer pro-alpha1(V)-pro-alpha1(V)-pro-alpha2(V). Mutations in this gene are associated with Ehlers-Danlos syndrome, types I and II. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, May 2013]
Expression
Broad expression in placenta (RPKM 45.0), endometrium (RPKM 38.1) and 16 other tissues See more
Orthologs
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Genomic context

Location:
9q34.3
Exon count:
68
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 9 NC_000009.12 (134641803..134844843)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 9 NC_060933.1 (146859174..147065950)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 9 NC_000009.11 (137533649..137736689)

Chromosome 9 - NC_000009.12Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105376311 Neighboring gene ReSE screen-validated silencer GRCh37_chr9:137338907-137339314 Neighboring gene Sharpr-MPRA regulatory region 11314 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr9:137346195-137347030 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:137347374-137348311 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:137348312-137349248 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr9:137353764-137354264 Neighboring gene H3K27ac hESC enhancer GRCh37_chr9:137367387-137367888 Neighboring gene uncharacterized LOC100506532 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr9:137385020-137385642 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr9:137410305-137410805 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr9:137414037-137414741 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr9:137430547-137431179 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:137437101-137437866 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr9:137444755-137445276 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr9:137445277-137445797 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr9:137446661-137447263 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 29285 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr9:137481596-137482127 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr9:137486667-137487168 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:137494155-137495067 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:137495068-137495979 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:137518819-137519400 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:137519401-137519982 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr9:137534628-137535334 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:137536590-137537174 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:137539157-137539956 Neighboring gene uncharacterized LOC124902300 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr9:137540681-137541180 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr9:137546641-137547505 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr9:137547506-137548369 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr9:137549426-137550233 Neighboring gene COL5A1 antisense RNA 1 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr9:137571911-137572432 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr9:137572433-137572952 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr9:137572953-137573473 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr9:137573474-137573993 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr9:137580636-137581426 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr9:137589714-137590538 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr9:137590539-137591361 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr9:137600147-137600714 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr9:137615715-137616537 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:137642670-137643182 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:137643183-137643695 Neighboring gene ReSE screen-validated silencer GRCh37_chr9:137644538-137644744 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 29286 Neighboring gene uncharacterized LOC124902301 Neighboring gene H3K27ac hESC enhancer GRCh37_chr9:137665167-137665668 Neighboring gene ReSE screen-validated silencer GRCh37_chr9:137669421-137669566 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr9:137670079-137670688 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr9:137676102-137677054 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr9:137696519-137697019 Neighboring gene uncharacterized LOC101448202 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr9:137733985-137734819 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr9:137737131-137737631 Neighboring gene microRNA 3689c Neighboring gene microRNA 3689a

Genomic regions, transcripts, and products

Expression

  • Project title: HPA RNA-seq normal tissues
  • Description: RNA-seq was performed of tissue samples from 95 human individuals representing 27 different tissues in order to determine tissue-specificity of all protein-coding genes
  • BioProject: PRJEB4337
  • Publication: PMID 24309898
  • Analysis date: Wed Apr 4 07:08:55 2018

Bibliography

GeneRIFs: Gene References Into Functions

What's a GeneRIF?

Phenotypes

Associated conditions

Description Tests
Ehlers-Danlos syndrome, classic type, 1
MedGen: C0268335 OMIM: 130000 GeneReviews: Classic Ehlers-Danlos Syndrome
Compare labs
Fibromuscular dysplasia, multifocal
MedGen: C5543412 OMIM: 619329 GeneReviews: Not available
Compare labs

Copy number response

Description
Copy number response
Triplosensitivity

No evidence available (Last evaluated 2017-12-14)

ClinGen Genome Curation Page
Haploinsufficency

Sufficient evidence for dosage pathogenicity (Last evaluated 2017-12-14)

ClinGen Genome Curation PagePubMed

EBI GWAS Catalog

Description
A genome-wide association study of central corneal thickness in Latinos.
EBI GWAS Catalog
Gene-age interactions in blood pressure regulation: a large-scale investigation with the CHARGE, Global BPgen, and ICBP Consortia.
EBI GWAS Catalog
Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus.
EBI GWAS Catalog
Joint influence of small-effect genetic variants on human longevity.
EBI GWAS Catalog
Multidimensional prognostic risk assessment identifies association between IL12B variation and surgery in Crohn's disease.
EBI GWAS Catalog
New loci associated with central cornea thickness include COL5A1, AKAP13 and AVGR8.
EBI GWAS Catalog
Population-based meta-analysis in Caucasians confirms association with COL5A1 and ZNF469 but not COL8A2 with central corneal thickness.
EBI GWAS Catalog

HIV-1 interactions

Replication interactions

Interaction Pubs
Knockdown of collagen, type V, alpha 1 (COL5A1) by siRNA inhibits the early stages of HIV-1 replication in 293T cells infected with VSV-G pseudotyped HIV-1 PubMed

Go to the HIV-1, Human Interaction Database

Pathways from PubChem

Interactions

Products Interactant Other Gene Complex Source Pubs Description

General gene information

Markers

Clone Names

  • FLJ45760

Gene Ontology Provided by GOA

Process Evidence Code Pubs
involved_in blood vessel development IEA
Inferred from Electronic Annotation
more info
 
involved_in cell adhesion IBA
Inferred from Biological aspect of Ancestor
more info
 
involved_in cell adhesion IMP
Inferred from Mutant Phenotype
more info
PubMed 
involved_in cell migration IMP
Inferred from Mutant Phenotype
more info
PubMed 
involved_in collagen biosynthetic process IMP
Inferred from Mutant Phenotype
more info
PubMed 
involved_in collagen fibril organization IBA
Inferred from Biological aspect of Ancestor
more info
 
involved_in collagen fibril organization IMP
Inferred from Mutant Phenotype
more info
PubMed 
involved_in collagen fibril organization NAS
Non-traceable Author Statement
more info
PubMed 
involved_in eye morphogenesis IMP
Inferred from Mutant Phenotype
more info
PubMed 
involved_in heart morphogenesis IEA
Inferred from Electronic Annotation
more info
 
involved_in integrin biosynthetic process IMP
Inferred from Mutant Phenotype
more info
PubMed 
involved_in negative regulation of endodermal cell differentiation IDA
Inferred from Direct Assay
more info
PubMed 
involved_in regulation of cellular component organization IEA
Inferred from Electronic Annotation
more info
 
involved_in skin development IMP
Inferred from Mutant Phenotype
more info
PubMed 
involved_in supramolecular fiber organization IMP
Inferred from Mutant Phenotype
more info
PubMed 
involved_in tendon development IEA
Inferred from Electronic Annotation
more info
 
involved_in wound healing, spreading of epidermal cells IMP
Inferred from Mutant Phenotype
more info
PubMed 

General protein information

Preferred Names
collagen alpha-1(V) chain
Names
collagen, type V, alpha 1

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

  1. NG_008030.1 RefSeqGene

    Range
    5000..208038
    Download
    GenBank, FASTA, Sequence Viewer (Graphics), LRG_737

mRNA and Protein(s)

  1. NM_000093.5NP_000084.3  collagen alpha-1(V) chain isoform 1 preproprotein

    See identical proteins and their annotated locations for NP_000084.3

    Status: REVIEWED

    Description
    Transcript Variant: This variant (1) encodes isoform 1.
    Source sequence(s)
    AB209864, AB371583, AI190929, AL591890, BC032405, BM051019, CA446007, CB152831, CN399221, CN399265, CN484933, ES314363
    Consensus CDS
    CCDS6982.1
    UniProtKB/Swiss-Prot
    A0A087WXW9, P20908, Q15094, Q5SUX4
    UniProtKB/TrEMBL
    B2ZZ86
    Related
    ENSP00000360882.3, ENST00000371817.8
    Conserved Domains (3) summary
    pfam01391
    Location:871930
    Collagen; Collagen triple helix repeat (20 copies)
    smart00210
    Location:39230
    TSPN; Thrombospondin N-terminal -like domains
    pfam01410
    Location:16101836
    COLFI; Fibrillar collagen C-terminal domain
  2. NM_001278074.1NP_001265003.1  collagen alpha-1(V) chain isoform 2 preproprotein

    Status: REVIEWED

    Description
    Transcript Variant: This variant (2) contains an alternate in-frame exon in the 3' coding region compared to variant 1. It encodes isoform 2 which is of the same length but contains an alternate segment, compared to isoform 1. This variant is based on experimental data in PMID 22149965 and is supported by partial transcripts and RNA-seq data.
    Source sequence(s)
    AB209864, AB371583, AI190929, AL591890, BC032405, BM051019, CA446007, CB152831, CN399198, CN399221, CN399265, CN484933, ES314363
    Consensus CDS
    CCDS75932.1
    UniProtKB/TrEMBL
    B2ZZ86
    Related
    ENSP00000360885.4, ENST00000371820.4
    Conserved Domains (3) summary
    pfam01391
    Location:871930
    Collagen; Collagen triple helix repeat (20 copies)
    smart00210
    Location:39230
    TSPN; Thrombospondin N-terminal -like domains
    pfam01410
    Location:16101836
    COLFI; Fibrillar collagen C-terminal domain

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2023_10

The following sections contain reference sequences that belong to a specific genome build. Explain

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000009.12 Reference GRCh38.p14 Primary Assembly

    Range
    134641803..134844843
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

mRNA and Protein(s)

  1. XM_017014266.3XP_016869755.1  collagen alpha-1(V) chain isoform X1

    UniProtKB/TrEMBL
    B2ZZ86

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060933.1 Alternate T2T-CHM13v2.0

    Range
    146859174..147065950
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

mRNA and Protein(s)

  1. XM_054361962.1XP_054217937.1  collagen alpha-1(V) chain isoform X1