Collagen, Type I, Alpha-1

Alternative Names

  • COL1A1
  • Collagen of Skin, Tendon, and Bone, Alpha-1 Chain
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OMIM Number

120150

NCBI Gene ID

1277

Uniprot ID

P02452

Length

17,554 bases

No. of Exons

51

No. of isoforms

1

Protein Name

Collagen alpha-1(I) chain

Molecular Mass

138941 Da

Amino Acid Count

1464

Genomic Location

chr17:50,184,095-50,201,648

Gene Map Locus
17q21.33

Description

COL1A1  gene encodes pro-alpha1 chains of type I collagen.  Type I collagen is the most abundant and widely expressed collagen in humans, found in most connective tissues, especially in bone, cornea, dermis, and tendon.  It is a heterotrimer comprising two alpha 1 chains and one alpha 2 chain. 

Mutations in this gene are associated with a variety of conditions, including osteogenesis imperfecta types I-IV, Ehlers-Danlos syndrome type VIIA, Ehlers-Danlos syndrome Classical type, Caffey Disease and idiopathic osteoporosis.

Epidemiology in the Arab World

View Map
Variant NameCountryGenomic LocationClinvar Clinical SignificanceCTGA Clinical Significance Condition(s)HGVS ExpressionsdbSNPClinvar
NM_000088.4:c.1273G>ASaudi ArabiaNC_000017.11:g.50195258C>TPathogenicLikely PathogenicOsteogenesis Imperfecta, Type ING_007400.1:g.11382G>A; NM_000088.4:c.1273G>A; NP_000079.2:p.Gly425Ser72648330647159
NM_000088.4:c.2127+2T>ASaudi ArabiaNC_000017.11:g.50191786A>TPathogenicPathogenicOsteogenesis Imperfecta, Type ING_007400.1:g.14854T>A; NM_000088.4:c.2127+2T>A72651644574055
NM_000088.4:c.2299G>AEgyptNC_000017.11:g.50190861C>TPathogenicPathogenicOsteogenesis Imperfecta, Type ING_007400.1:g.15779G>A; NM_000088.4:c.2299G>A; NP_000079.2:p.Gly767Ser72651658546096
NM_000088.4:c.299-2A>GSaudi ArabiaNC_000017.11:g.50199592T>CPathogenicOsteogenesis Imperfecta, Type ING_007400.1:g.7048A>G; NM_000088.4:c.299-2A>G
NM_000088.4:c.841G>ASaudi ArabiaNC_000017.11:g.50196634C>TPathogenicLikely PathogenicOsteogenesis Imperfecta, Type ING_007400.1:g.10006G>A; NM_000088.4:c.841G>A; NP_000079.2:p.Gly281Ser72645334425590

Other Reports

Saudi Arabia

Linjawi et al, (2016) recruited 47 patients with scars and 37 healthy controls to evaluate the association of COL1A1 SNPs with scar formation.  About 32 of the 47 patients had keloid scars, while the rest had hypertrophic scars.  Genotyping study found that there was significant association between –1997 G/T (rs1107946) polymorphism in the COL1A1 gene and scar formation, especially in female participants.  In addition, no association between +1245 G/T (rs1800012) polymorphism and scars was found.  The authors suggested that GG haplotype was responsible for enhancing the transcriptional activity of the COL1A1 gene.  Therefore, they suggested further investigations to explain the relationship between susceptibility to scars and COL1A1 gene expression.

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