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. 2020 Aug 14;7:9. doi: 10.1186/s40348-020-00101-9

Table 1.

A list of these genes together with the encoded proteins that are changed as well as the mode of inheritance

Gene OMIM gene Protein Phenotype OMIM phenotype
Autosomal-dominant inheritance
COL1A1 120150 Collagen α1(I) chain (COL1A1)

OI type I

OI type II

OI type III

OI type IV

166200

166210

259420

166220

COL1A2 120160 Collagen α2(I) chain (COL1A2)
IFITM5 614757

Interferon-induced transmembrane protein 5 (IFITM5)

Alternative: Bone-restricted interferon-induced transmembrane protein-like protein (BRIL)

OI type V 610967
P4HB 176790

Protein disulfide-isomerase (PDI)

alternative: Prolyl 4-hydroxylase subunit beta (P4HB)

Cole-Carpenter syndrome type 1 112240
Autosomal-recessive inheritance
SERPINF1 172860 Pigment epithelium-derived factor (PEDF) OI type VI 613982
CRTAP 605497 Cartilage-associated protein (CRTAP) OI type VII 610682
P3H1 610339 Prolyl 3-hydroxylase 1 (P3H1) P3H1 610339
PPIB 123841

Peptidyl-prolyl cis-trans isomerase B (PPIB)

Alternative: Cyclophilin B

OI type IX 259440
SERPINH1 600943

Serpin peptidase inhibitor, clade H, member 1 (Serpin H1)

Alternative: Heat shock protein 47 (HSP47)

OI type X 613848
FKBP10 607063

Peptidyl-prolyl cis-trans isomerase FKBP10 (PPIase FKBP10)

Alternative: 65 kDa FK506-binding protein (FKBP65)

Bruck syndrome type 1

OI type XI

259450

610968

SP7 606633

Transcription factor Sp7

Alternative: Zinc finger protein osterix

OI type XII 613849
BMP1 112264 Bone morphogenetic protein 1 (BMP1) OI type XIII 614856
TMEM38B 611236

Trimeric intracellular cation channel type B (TRIC-B)

Alternative: Transmembrane protein 38B (TMEM38B)

OI type XIV 615066
WNT1 164820 Proto-oncogene Wnt1 (wingless-type MMTV integration site family, member 1, WNT1) OI type XV 615220
CREB3L1 616215 Cyclic AMP-responsive element-binding protein 3-like protein 1 (CR3L1) OI type XVI 616229
SPARC 182120 Secreted protein acidic and rich in cysteine (SPARC) OI type XVII 616507
TENT5A 611357

Terminal nucleotidyltransferase 5A (TENT5A)

Alternative: Family with sequence similarity 46, member A (FAM46A)

OI type XVIII 617952
MESD 607783 Mesoderm development LRP chaperone (MESD) OI type XX 618644
PLOD2 601865

Procollagen-lysine,2-oxoglutarate 5-dioxygenase 2 (PLOD2)

Alternative: Lysyl hydroxylase 2 (LH2)

Bruck syndrome type 2 609220
SEC24D 607186

Protein transport protein Sec24D (SEC24D)

Alternative: SEC24-related protein D

Cole-Carpenter syndrome type 2 616294
X-linked inheritance
MBTPS2 300294

Membrane-bound transcription factor site-2 protease (MBTPS2)

Alternative: Endopeptidase S2P

OI type XIX 301014
PLS3 300131 Plastin-3 (PLS3) Osteoporosis (X-linked dominant) 300910