The detail information of Osteogenesis imperfecta, COL1A2-related
OMIA Basic Information

Possible human homologues (MIM numbers):

Mendelian trait/disorder: yes

Mode of inheritance: Autosomal Dominant

Considered a defect: yes

Year key mutation first reported: 2001

Species-specific name: -

Species-specific symbol: -

More detail information can see in

Associated Breeds
iDog Breed Number Breed Name Personality Height Weight History Breed Source
CB24 English Beagle 33 cm & under 33-38.1 cm under 9.1 kg (5.9 inches & under), 9.1-13.6 kg (5.9-6.8 inches) United Kingdom (England)
Associated Gene
There are no associated genes.
References
Note: the references are listed in reverse chronological order (from the most recent year to the earliest year), and alphabetically by first author within a year.
2019 Letko,A.,Zdora,I.,Hitzler,V.,Jagannathan,V.,Beineke,A.,Möhrke,C.,Drögemüller,C.,Letko,A.,Zdora,I.,Hitzler,V.,Jagannathan,V.,Beineke,A.,Möhrke,C.,Drögemüller,C.: :
A de novo in-frame duplication in the COL1A2 gene in a Lagotto Romagnolo dog with osteogenesis imperfecta. Anim Genet :, 2019.
Pubmed reference: 31468557 . DOI: 10.1111/age.12843 .
2017 Quist,E.M.,Doan,R.,Pool,R.R.,Porter,B.F.,Bannasch,D.L.,Dindot,S.V.: :
Identification of a candidate mutation in the COL1A2 gene of a Chow Chow with osteogenesis imperfecta. J Hered :, 2017.
Pubmed reference: 29036614 . DOI: 10.1093/jhered/esx074 .
2001 Campbell,B.G.,Wootton,J.A.M.,Macleod,J.N.,Minor,R.R.: :
Canine COL1A2 mutation resulting in C-terminal truncation of pro-alpha 2(I) and severe osteogenesis imperfecta Journal of Bone & Mineral Research 16:1147-1153, 2001.
Pubmed reference: 11393792 . DOI: 10.1359/jbmr.2001.16.6.1147 .