- 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 |
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 |
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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