1. Gene
  2. COL21A1 - collagen type XXI alpha 1 chain Gene

COL21A1 - collagen type XXI alpha 1 chain Gene

Homo sapiens

Also known as FP633; COLA1L

Gene ID: 81578 | Gene type: protein coding

About COL21A1

Cytogenetic location: 6p12.1 Genomic coordinates (GRCh38): 6:56,056,590-56,394,128 (from NCBI)

This gene has 12 transcripts (splice variants), 109 orthologues and 37 paralogues. Broad expression in placenta (RPKM 9.8), heart (RPKM 8.6) and 16 other tissues.

Summary

This gene encodes the alpha chain of type XXI collagen, a member of the FACIT (fibril-associated collagens with interrupted helices) collagen family. Type XXI collagen is localized to tissues containing type I collagen and maintains the integrity of the extracellular matrix. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]

COL21A1 Products(5)

mRNA Protein Name
NM_001318751.2 NP_001305680.1 collagen alpha-1(XXI) chain isoform a precursor
NM_001318752.2 NP_001305681.1 collagen alpha-1(XXI) chain isoform b precursor
NM_001318753.2 NP_001305682.1 collagen alpha-1(XXI) chain isoform c
NM_001318754.2 NP_001305683.1 collagen alpha-1(XXI) chain isoform d
NM_030820.4 NP_110447.2 collagen alpha-1(XXI) chain isoform a precursor

COL21A1 Protein Structure

VWA

VWA: von Willebrand factor type A domain (37 - 206)

Collagen

Collagen: Collagen triple helix repeat (20 copies) (448 - 500)

Collagen

Collagen: Collagen triple helix repeat (20 copies) (486 - 542)

Collagen

Collagen: Collagen triple helix repeat (20 copies) (536 - 594)

Collagen

Collagen: Collagen triple helix repeat (20 copies) (681 - 733)

Collagen

Collagen: Collagen triple helix repeat (20 copies) (731 - 787)

Collagen

Collagen: Collagen triple helix repeat (20 copies) (825 - 882)

Collagen

Collagen: Collagen triple helix repeat (20 copies) (884 - 934)

  • 0
  • 200
  • 400
  • 600
  • 800
  • 957 a.a.
Protein Preferred Names Protein Names

collagen alpha-1(XXI) chain

alpha 1 chain-like collagen

Recombinant COL21A1 Proteins

Cat. No. Product Name Accession Purity
HY-P70094 COL21A1 Protein, Human (HEK293, His) Q96P44 (E23-Y957) ≥95%

Related Diseases

Diseases Alias
Ullrich Congenital Muscular Dystrophy 1

Ullrich Congenital Muscular Dystrophy

Ullrich Disease

Ucmd

Ullrich Scleroatonic Muscular Dystrophy

Scleroatonic Muscular Dystrophy

UCMD1

Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 22

Lgmdr22

Muscular Dystrophy, Scleroatonic

Late Onset Scleroatonic Familial Myopathy

Congenital Muscular Dystrophy, Ullrich Type

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma