- abnormal organ of Corti morphology / MGI
- abnormal semicircular canal morphology / MGI
- abnormal cochlear hair cell morphology / MGI
- head shaking / MGI
- abnormal crista ampullaris morphology / MGI
- increased cochlear inner hair cell number / MGI
- decreased cochlear outer hair cell number / MGI
- head tossing / MGI
- hearing/vestibular/ear phenotype / MGI
- abnormal semicircular canal ampulla morphology / MGI
- enlarged pericardium / MGI
- abnormal blood vessel morphology / MGI
- hemorrhage / MGI
- abnormal vitelline vasculature morphology / MGI
- kinked neural tube / MGI
- embryonic growth retardation / MGI
- embryonic lethality during organogenesis, complete penetrance / MGI
- embryonic lethality during organogenesis / MGI
- embryo tissue necrosis / MGI
C3HeB/FeJ-Jag1Mhdahtu/Ieg
Status | Available to order |
EMMA ID | EM:00199 |
International strain name | C3HeB/FeJ-Jag1Mhdahtu/Ieg |
Alternative name | ABE2 |
Strain type | Induced Mutant Strains : Chemically-induced |
Allele/Transgene symbol | Jag1Mhdahtu, |
Gene/Transgene symbol | Jag1 |
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 | ENU-induced mutation of Jag1. Strains EM:00199 and EM:04920 carry the same mutant allele. Strain EM:00199 has been backcrossed around 5 times to C3HeB/FeJ. Strain EM:04920 has possibly been further backcrossed 1/2 times to C3HeB/FeJ. |
Phenotypic information | Head tossing. |
Breeding history | Around 5 times backcrossed to C3HeB/FeJ. |
References |
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Information from EMMA
Archiving centre | Helmholtz Zentrum Muenchen - German Research Center for Environmental Health (GmbH), Oberschleißheim, Germany |
Disease and phenotype information
MGI allele-associated human disease models
Orphanet associated rare diseases, based on orthologous gene matching
- Tetralogy of Fallot / Orphanet_3303
- Alagille syndrome due to a JAG1 point mutation / Orphanet_261619
MGI phenotypes (allele matching)
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
- The Notch ligand Jagged1 is required for inner ear sensory development.;Kiernan A E, Ahituv N, Fuchs H, Balling R, Avraham K B, Steel K P, Hrabé de Angelis M, ;2001;Proceedings of the National Academy of Sciences of the United States of America;98;3873-8; 11259677
- 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
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