C3HeB/FeJ-CasrBCH004/Ieg

Status

Available to order

EMMA IDEM:02558
International strain nameC3HeB/FeJ-CasrBCH004/Ieg
Alternative nameBCH004
Strain typeInduced Mutant Strains : Chemically-induced
Allele/Transgene symbolCasrBCH004
Gene/Transgene symbolCasr

Information from provider

ProviderMartin Hrabe de Angelis
Provider affiliationInstitute of Experimental Genetics, Helmholtz Zentrum Muenchen - German Research Center for Environmental Health (GmbH)
Genetic informationMutation in exon 4 of Casr gene, c.1366 G to T, p.456 Glu to stop.
Phenotypic informationCalcium high.
Breeding historyMore than 2 times backcrossed to C3HeB/FeJ.
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
Homozygous fertilenot known
Homozygous viablenot known
Homozygous matings requiredno
Immunocompromisedno

Information from EMMA

Archiving centreHelmholtz Zentrum Muenchen - German Research Center for Environmental Health (GmbH), Oberschleißheim, Germany
Animals used for archivingheterozygous C3H

Disease and phenotype information

MGI allele-associated human disease models

Orphanet associated rare diseases, based on orthologous gene matching

IMPC phenotypes (gene matching)
  • increased circulating calcium level / IMPC
  • decreased prepulse inhibition / IMPC
  • edema / IMPC
  • abnormal pancreas morphology / IMPC
  • small superior vagus ganglion / IMPC
  • increased circulating phosphate level / IMPC
  • preweaning lethality, complete penetrance / IMPC
  • enlarged uterus / IMPC
MGI phenotypes (allele matching)
  • increased circulating calcium level / MGI
MGI phenotypes (gene matching)
  • delayed bone ossification / MGI
  • decreased bone mineral density / MGI
  • kyphoscoliosis / MGI
  • increased circulating calcium level / MGI
  • decreased circulating calcium level / MGI
  • decreased circulating phosphate level / MGI
  • decreased body weight / MGI
  • decreased body size / MGI
  • cataract / MGI
  • dehydration / MGI
  • aphagia / MGI
  • abnormal posture / MGI
  • increased circulating phosphate level / MGI
  • postnatal growth retardation / MGI
  • abnormal coat/hair pigmentation / MGI
  • premature death / MGI
  • increased hematocrit / MGI
  • abnormal bone mineralization / MGI
  • decreased urine phosphate level / MGI
  • increased circulating parathyroid hormone level / MGI
  • decreased circulating parathyroid hormone level / MGI
  • abnormal postural reflex / MGI
  • decreased urine calcium level / MGI
  • enlarged parathyroid gland / MGI
  • pigmented parathyroid gland / MGI
  • rickets / MGI
  • calcinosis / MGI
  • nephrocalcinosis / MGI
  • calcified muscle / MGI
  • increased width of hypertrophic chondrocyte zone / MGI
  • parathyroid gland hyperplasia / MGI
  • lethargy / MGI
  • renal/urinary system phenotype / MGI
  • growth/size/body region phenotype / MGI
  • endocrine/exocrine gland phenotype / MGI
  • skeleton phenotype / MGI
  • hematopoietic system phenotype / MGI
  • increased circulating magnesium level / MGI
  • postnatal lethality, complete penetrance / MGI
  • abnormal parathyroid gland chief cell morphology / MGI
  • tongue inflammation / 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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Practical information

Genotyping protocol

Example health report
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Material Transfer Agreement (MTA)
Distribution of this strain is subject to a provider MTA. Both signing of the MTA and submission of the online EMMA Mutant Request Form are required before material can be shipped.

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Legally binding conditions for the transfer

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