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Former Names T30H (Changed: 15-DEC-04 ) Type Chromosome Aberration; Translocation; Additional information on Mice with Chromosomal Aberrations. Type Mutant Stock; Additional information on Genetically Engineered and Mutant Mice. Visit our online Nomenclature tutorial. Species laboratory mouse
Reciprocal Translocations
View Reciprocal Translocations (46 strains)
Strains carrying Gdf5bp-H allele
000251 AEJ.Cg-ae +/a Gdf5bp-H/J View Strains carrying Gdf5bp-H (1 strain)
Strains carrying a allele
View Strains carrying a (104 strains)
Strains carrying other alleles of Gdf5
002239 B6 x BALB/cJ-Gdf5bp-3J/J View Strains carrying other alleles of Gdf5 (1 strain)
Strains carrying other alleles of a
View Strains carrying other alleles of a (81 strains)
View Research Applications
Research Applications
This mouse can be used to support research in many areas including:
Gdf5bp-H relatedResearch Tools
Genetics Research
Gdf5bp-J relatedDevelopmental Biology Research
Growth Defects
Mouse/Human Gene Homologs
acromesomelic dysplasia, Hunter-Thompson Type
Developmental Biology Research
Growth Defects
Mouse/Human Gene Homologs
acromesomelic dysplasia, Hunter-Thompson Type
| Allele Symbol | Gdf5bp-H | ||
|---|---|---|---|
| Allele Name | brachypodism Harwell | ||
| Allele Type | Spontaneous | ||
| Strain of Origin | PCT | ||
| Gene Symbol and Name | Gdf5, growth differentiation factor 5 | ||
| Chromosome | 2 | ||
| Gene Common Name(s) | BMP14; CDMP-1; CDMP1; LAP4; OS5; SYNS2; bp; brachypod Japan; brachypodism; brp; cartilage-derived morphogenetic protein-1; | ||
| General Note | This remutation arose spontaneously at Harwell in the PCT multiple recessive stock (J:13391). It is essentially identical in effect with Gdf5bp, and has been used extensively in studies of brachypodism. Dissociated mesoderm cells from 12-day hindlimb buds of Gdfbp-H homozygous mutant embryos make fewer and smaller condensations than those of control embryos and chondrogenesis is delayed (J:12041). Cells of the limb mesenchyme are more adhesive than in normal embryos (J:6104). Cell aggregation and cartilaginous nodule formation were determined in cultures of various combinations of cells from different stages and parts of limb buds of 10- to 13-day embryos. In limb buds from mice homozygous for Gdf5bp-H, there is reduced ability of a specific mesenchyme cell population to provide inductive stimulus for chondrogenesis. This cell-cell interaction results in a lower proportion of chondrogenic cells and a higher proportion of more mature non-chondrogenic cells. A factor produced by the femur and fibula or by the postaxial part of the hindlimb bud of 13-day Gdf5bp-H homozygous mutant mice inhibits the growth in vitro of tibias of 13-day wild-typeembryos (J:5444). Although tibias from 13-day mutant embryos grow normally in standard cultures, addition of a factor from the postaxial part of limb buds from 11- to 12-day wild-type mice causes reduces growth of mutant but not of wild-type 13-day tibias (J:11997). In an in vitro system which supports autonomous development of individual limb elements, the proximal-to-distal increase of severity of cartilage reduction is intensified in explants from homozygous mutant mice. (J:942). | ||
| Allele Symbol | Gdf5bp-J | ||
| Allele Name | brachypodism Jackson | ||
| Allele Type | Spontaneous | ||
| Common Name(s) | GdfbpJ; | ||
| Strain of Origin | A/J | ||
| Gene Symbol and Name | Gdf5, growth differentiation factor 5 | ||
| Chromosome | 2 | ||
| Gene Common Name(s) | BMP14; CDMP-1; CDMP1; LAP4; OS5; SYNS2; bp; brachypod Japan; brachypodism; brp; cartilage-derived morphogenetic protein-1; | ||
| General Note | The long bones of the limbs of mutant mice are slightly shorter than controls, and the fibula is shortened proximally. The bones of the axial skeleton are unaffected. | ||
| Molecular Note | This remutation to brachypodism occurred in the A/J strain at The Jackson Laboratory. The mutation is caused by the insertion of a guanine residue into a stretch of three guanine residues in the gene sequence (position 1444-1448), producing a stop codon 41 amino acids later. [MGI Ref ID J:17582] | ||
| Allele Symbol | a | ||
| Allele Name | nonagouti | ||
| Allele Type | Spontaneous | ||
| Gene Symbol and Name | T(2;11)30H, reciprocal translocation, Chr 2 and 11, Harwell 30 | ||
| Chromosome | 11 | ||
| Gene Common Name(s) | T30H; | ||
This strain will not have a genotyping protocol or one is not currently available.
Helpful Links
Genotyping resources and troubleshooting
Gdf5bp-H relatedGdf5bp-J relatedBugrilova RS; Konyukhov BV. 1978. Regulator of the expression of the gene brachypodism-H in the mouse. Sov Genet 14:1272-1278. [MGI Ref ID J:11997]
Duke J; Elmer WA. 1978. Cell adhesion and chondrogenesis in brachypod mouse limb mesenchyme: fragment fusion studies. J Embryol Exp Morphol 48:161-8. [PubMed: 744946] [MGI Ref ID J:6104]
Duke J; Elmer WA. 1977. Effect of the brachypod mutation on cell adhesion and chondrogenesis in aggregates of mouse limb mesenchyme. J Embryol Exp Morphol 42:209-217. [MGI Ref ID J:12041]
Kwasigroch TE; Curtis SK; Knudsen TB; Barrach HJ; Elmer WA. 1992. Morphological analysis of abnormal digital chondrogenesis in the brachypod (bpH) mouse limb in organ culture. Anat Embryol (Berl) 185(4):307-15. [PubMed: 1609959] [MGI Ref ID J:942]
Lyon MF. 1958. brachypody, bp Mouse News Lett 19:22. [MGI Ref ID J:13391]
Owens EM; Solursh M. 1983. Accelerated maturation of limb mesenchyme by the BrachypodH mouse mutation. Differentiation 24(2):145-8. [PubMed: 6309591] [MGI Ref ID J:7163]
Owens EM; Solursh M. 1982. Cell-cell interaction by mouse limb cells during in vitro chondrogenesis: analysis of the brachypod mutation. Dev Biol 91(2):376-88. [PubMed: 7095270] [MGI Ref ID J:6808]
Pleskova MV; Rodionov VM; Bugrilova RS; Konyukhov BV. 1974. The partial purification of growth-inhibiting factor of the brachypodism-H mouse embryos. Dev Biol 37(2):417-21. [PubMed: 4826284] [MGI Ref ID J:5444]
Baur ST; Mai JJ; Dymecki SM. 2000. Combinatorial signaling through BMP receptor IB and GDF5: shaping of the distal mouse limb and the genetics of distal limb diversity. Development 127(3):605-19. [PubMed: 10631181] [MGI Ref ID J:59288]
Clark RT; Johnson TL; Schalet BJ; Davis L; Gaschen V; Hunziker EB; Oldberg A; Mikic B. 2001. GDF-5 deficiency in mice leads to disruption of tail tendon form and function. Connect Tissue Res 42(3):175-86. [PubMed: 11913489] [MGI Ref ID J:117311]
Kanauchi Y; Takahara M; Harada M; Ogino T. 2008. Growth of severely hypoplastic phalanges and metacarpals in symbrachydactyly: an experimental study in mice. J Hand Surg [Am] 33(9):1589-96. [PubMed: 18984342] [MGI Ref ID J:143089]
Mikic B; Battaglia TC; Taylor EA; Clark RT. 2002. The effect of growth/differentiation factor-5 deficiency on femoral composition and mechanical behavior in mice. Bone 30(5):733-7. [PubMed: 11996912] [MGI Ref ID J:109392]
Mikic B; Schalet BJ; Clark RT; Gaschen V; Hunziker EB. 2001. GDF-5 deficiency in mice alters the ultrastructure, mechanical properties and composition of the Achilles tendon. J Orthop Res 19(3):365-71. [PubMed: 11398847] [MGI Ref ID J:113154]
Settle SH Jr; Rountree RB; Sinha A; Thacker A; Higgins K; Kingsley DM. 2003. Multiple joint and skeletal patterning defects caused by single and double mutations in the mouse Gdf6 and Gdf5 genes. Dev Biol 254(1):116-30. [PubMed: 12606286] [MGI Ref ID J:83132]
Storm EE; Huynh TV; Copeland NG; Jenkins NA; Kingsley DM; Lee SJ. 1994. Limb alterations in brachypodism mice due to mutations in a new member of the TGF beta-superfamily [see comments] Nature 368(6472):639-43. [PubMed: 8145850] [MGI Ref ID J:17582]
Storm EE; Kingsley DM. 1996. Joint patterning defects caused by single and double mutations in members of the bone morphogenetic protein (BMP) family. Development 122(12):3969-79. [PubMed: 9012517] [MGI Ref ID J:38423]
Takahara M; Harada M; Guan D; Otsuji M; Naruse T; Takagi M; Ogino T. 2004. Developmental failure of phalanges in the absence of growth/differentiation factor 5. Bone 35(5):1069-76. [PubMed: 15542031] [MGI Ref ID J:94510]
Yi SE; Daluiski A; Pederson R; Rosen V; Lyons KM. 2000. The type I BMP receptor BMPRIB is required for chondrogenesis in the mouse limb. Development 127(3):621-30. [PubMed: 10631182] [MGI Ref ID J:59282]
Currently there no information available for this strain. This may be due to the supply level of this strain.
| Pricing for USA, Canada and Mexico shipping destinations |
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Animals Provided
Price (US dollars $) Cryorecovery Fee $1900.00 At least two mice that carry the mutation (if it is a mutant strain) will be provided. Their genotypes may not reflect those discussed in the strain description. Please inquire for possible genotypes and see additional details below.
| Pricing for International shipping destinations |
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Animals Provided
Price (US dollars $) Cryorecovery Fee $2470.00 At least two mice that carry the mutation (if it is a mutant strain) will be provided. Their genotypes may not reflect those discussed in the strain description. Please inquire for possible genotypes and see additional details below.
| Standard Supply | Cryopreserved. Ready for recovery. Please refer to pricing and supply notes for further information. |
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| Supply Notes |
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