- abnormal craniofacial morphology / MGI
- absent facial nuclei / MGI
- abnormal facial motor nucleus morphology / MGI
- small facial motor nucleus / MGI
- decreased sensory neuron number / MGI
- abnormal facial nerve morphology / MGI
- decreased body size / MGI
- abnormal reflex / MGI
- abnormal tooth morphology / MGI
- no abnormal phenotype detected / MGI
- abnormal axon guidance / MGI
- no phenotypic analysis / MGI
- nervous system phenotype / MGI
- abnormal nervous system morphology / MGI
- abnormal masseter muscle morphology / MGI
- abnormal temporalis muscle morphology / MGI
- absent facial nerve / MGI
- behavior/neurological phenotype / MGI
- abnormal neuron differentiation / MGI
- postnatal lethality, incomplete penetrance / MGI
- neonatal lethality, incomplete penetrance / MGI
- abnormal cochlear VIII nucleus morphology / MGI
- abnormal lower lip morphology / MGI
- abnormal rhombomere 4 morphology / MGI
- absent facial muscle / MGI
- narrow face / MGI
- facial paralysis / MGI
- facial muscle degeneration / MGI
- abnormal digastric posterior belly morphology / MGI
- abnormal buccinator muscle morphology / MGI
- abnormal depressor anguli oris muscle morphology / MGI
- abnormal zygomaticus muscle morphology / MGI
- absent levator nasolabialis muscle / MGI
C3HeB/FeJ-Hoxb1m1Mhda/Ieg
Status | Available to order |
EMMA ID | EM:10203 |
Citation information | RRID:IMSR_EM:10203 Research Resource Identifiers (RRID) are persistent unique ID numbers assigned to help researchers cite key resources (e.g. antibodies, model organisms and software projects) in the biomedical literature to improve transparency and reproducibility in research. See https://www.rrids.org/ for more information. |
International strain name | C3HeB/FeJ-Hoxb1m1Mhda/Ieg |
Alternative name | C3HeB/FeJ-Hoxb1T207AMhda |
Strain type | Induced Mutant Strains : Chemically-induced |
Allele/Transgene symbol | Hoxb1m1Mhda |
Gene/Transgene symbol | Hoxb1 |
Information from provider
Provider | Martin Hrabe de Angelis |
Provider affiliation | Institute of Experimental Genetics, Helmholtz Zentrum München |
Genetic information | Exon 2 c.619 A to G, p.Thr207Ala; PROVEAN prediction: -4.105 (deleterious). |
Phenotypic information | Homozygous:Not phenotyped.Heterozygous:Not phenotyped. |
Breeding history | Outcrossed candidate gene obtained by next generation sequencing of ENU mutagenesis-derived mutant lines. |
References | None available |
Homozygous fertile | not known |
Homozygous viable | yes |
Homozygous matings required | not known |
Immunocompromised | not known |
Information from EMMA
Archiving centre | Helmholtz Zentrum Muenchen - German Research Center for Environmental Health (GmbH), Oberschleißheim, Germany |
Animals used for archiving | homozygous C3H males |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Congenital hereditary facial paralysis-variable hearing loss syndrome / Orphanet_306530
MGI phenotypes (gene matching)
Information on how we integrate external resources can be found here
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