- abnormal vertebral arch morphology / IMPC
- short tail / IMPC
- decreased blood urea nitrogen level / IMPC
- decreased heart weight / IMPC
- decreased body length / IMPC
- abnormal vertebrae morphology / IMPC
- decreased circulating calcium level / IMPC
- thin tail / IMPC
- abnormal body size / IMPC
- abnormal radius morphology / IMPC
- abnormal ulna morphology / IMPC
- abnormal bone mineralization / IMPC
- decreased circulating phosphate level / IMPC
- decreased circulating amylase level / IMPC
- decreased body weight / IMPC
- decreased circulating triglyceride level / IMPC
- increased circulating potassium level / IMPC
- abnormal joint morphology / IMPC
- decreased bone mineral density / IMPC
- abnormal tail movements / IMPC
- abnormal tibia morphology / IMPC
- increased circulating alkaline phosphatase level / IMPC
- increased bone mineral content / IMPC
- abnormal tail morphology / IMPC
C3HeB/FeJ-PhexMhdabap012/Ieg
Status | Available to order |
EMMA ID | EM:02439 |
International strain name | C3HeB/FeJ-PhexMhdabap012/Ieg |
Alternative name | BAP012 |
Strain type | Induced Mutant Strains : Chemically-induced |
Allele/Transgene symbol | PhexMhdabap012 |
Gene/Transgene symbol | Phex |
Information from provider
Provider | Martin Hrabe de Angelis |
Provider affiliation | Institute of Experimental Genetics, Helmholtz Zentrum Muenchen - German Research Center for Environmental Health (GmbH) |
Genetic information | Mutation in exon 2 of Phex gene at position 148, A to T (aminoacid 50: Lys to STOP). |
Phenotypic information | High alkaline phosphatase. |
Breeding history | More than 2 times backcrossed to C3HeB/FeJ. |
References |
|
Homozygous fertile | not known |
Homozygous viable | not known |
Homozygous matings required | no |
Immunocompromised | no |
Information from EMMA
Archiving centre | Helmholtz Zentrum Muenchen - German Research Center for Environmental Health (GmbH), Oberschleißheim, Germany |
Animals used for archiving | heterozygous C3H |
Disease and phenotype information
MGI allele-associated human disease models
Orphanet associated rare diseases, based on orthologous gene matching
- X-linked hypophosphatemia / Orphanet_89936
IMPC phenotypes (gene matching)
MGI phenotypes (gene matching)
- decreased bone mineral density / MGI
- short mandible / MGI
- short premaxilla / MGI
- abnormal long bone metaphysis morphology / MGI
- decreased compact bone thickness / MGI
- abnormal vertebrae morphology / MGI
- abnormal rib morphology / MGI
- decreased circulating calcium level / MGI
- decreased circulating phosphate level / MGI
- abnormal cranium morphology / MGI
- domed cranium / MGI
- short limbs / MGI
- abnormal hindlimb morphology / MGI
- short tail / MGI
- decreased body length / MGI
- decreased body weight / MGI
- decreased body size / MGI
- circling / MGI
- abnormal gait / MGI
- abnormal osteoclast physiology / MGI
- abnormal intestinal absorption / MGI
- postnatal growth retardation / MGI
- abnormal postnatal growth/weight/body size / MGI
- disproportionate dwarf / MGI
- abnormal caudal vertebrae morphology / MGI
- short tibia / MGI
- short fibula / MGI
- abnormal cranial suture morphology / MGI
- abnormal bone mineralization / MGI
- increased urine phosphate level / MGI
- increased circulating parathyroid hormone level / MGI
- abnormal joint morphology / MGI
- decreased circulating alkaline phosphatase level / MGI
- increased circulating alkaline phosphatase level / MGI
- decreased urine calcium level / MGI
- abnormal long bone epiphyseal plate morphology / MGI
- short femur / MGI
- rickets / MGI
- increased width of hypertrophic chondrocyte zone / MGI
- increased activity of parathyroid / MGI
- maternal effect / MGI
- abnormal long bone morphology / MGI
- abnormal bone structure / MGI
- small clavicle / MGI
- short humerus / MGI
- short radius / MGI
- short ulna / MGI
- short frontal bone / MGI
- short nasal bone / MGI
- abnormal pelvic girdle bone morphology / MGI
- small vertebrae / MGI
- small caudal vertebrae / MGI
- decreased length of long bones / MGI
- decreased bone resorption / MGI
- renal/urinary system phenotype / MGI
- cellular phenotype / MGI
- cardiovascular system phenotype / MGI
- abnormal skeleton morphology / MGI
- increased diameter of femur / MGI
- decreased cranium height / MGI
- osteomalacia / MGI
- abnormal blood homeostasis / MGI
- exostosis / MGI
- decreased intestinal calcium absorption / MGI
- abnormal limb long bone morphology / MGI
- camptomelia / MGI
- abnormal obturator foramen morphology / MGI
- abnormal acetabulum morphology / MGI
- abnormal costochondral joint morphology / MGI
Literature references
- Genome-wide, large-scale production of mutant mice by ENU mutagenesis.;Hrabé de Angelis M H, Flaswinkel H, Fuchs H, Rathkolb B, Soewarto D, Marschall S, Heffner S, Pargent W, Wuensch K, Jung M, Reis A, Richter T, Alessandrini F, Jakob T, Fuchs E, Kolb H, Kremmer E, Schaeble K, Rollinski B, Roscher A, Peters C, Meitinger T, Strom T, Steckler T, Holsboer F, Klopstock T, Gekeler F, Schindewolf C, Jung T, Avraham K, Behrendt H, Ring J, Zimmer A, Schughart K, Pfeffer K, Wolf E, Balling R, ;2000;Nature genetics;25;444-7; 10932192
- Screening for dysmorphological abnormalities--a powerful tool to isolate new mouse mutants.;Fuchs H, Schughart K, Wolf E, Balling R, Hrabé de Angelis M, ;2000;Mammalian genome : official journal of the International Mammalian Genome Society;11;528-30; 10886017
- New mouse models for metabolic bone diseases generated by genome-wide ENU mutagenesis.;Sabrautzki Sibylle, Rubio-Aliaga Isabel, Hans Wolfgang, Fuchs Helmut, Rathkolb Birgit, Calzada-Wack Julia, Cohrs Christian M, Klaften Matthias, Seedorf Hartwig, Eck Sebastian, Benet-Pagès Ana, Favor Jack, Esposito Irene, Strom Tim M, Wolf Eckhard, Lorenz-Depiereux Bettina, Hrabě de Angelis Martin, ;2012;Mammalian genome : official journal of the International Mammalian Genome Society;23;416-30; 22527485
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