- vasculature congestion / MGI
- abnormal medulla oblongata morphology / MGI
- small facial motor nucleus / MGI
- abnormal motor neuron morphology / MGI
- abnormal sympathetic ganglion morphology / MGI
- abnormal parasympathetic ganglion morphology / MGI
- abnormal enteric nervous system morphology / MGI
- abnormal enteric ganglia morphology / MGI
- abnormal cranial nerve morphology / MGI
- absent trigeminal nerve / MGI
- abnormal vagus nerve morphology / MGI
- abnormal cranial ganglia morphology / MGI
- abnormal geniculate ganglion morphology / MGI
- abnormal petrosal ganglion morphology / MGI
- abnormal nodose ganglion morphology / MGI
- small trigeminal ganglion / MGI
- abnormal glossopharyngeal ganglion morphology / MGI
- abnormal vagus ganglion morphology / MGI
- cyanosis / MGI
- abnormal lung volume / MGI
- abnormal respiration / MGI
- abnormal breathing pattern / MGI
- respiratory failure / MGI
- apnea / MGI
- postnatal lethality / MGI
- abnormal eye morphology / MGI
- abnormal cardiovascular system morphology / MGI
- no abnormal phenotype detected / MGI
- hypoventilation / MGI
- abnormal respiratory function / MGI
- abnormal pulmonary ventilation / MGI
- mydriasis / MGI
- abnormal autonomic nervous system morphology / MGI
- abnormal carotid body morphology / MGI
- abnormal nervous system morphology / MGI
- abnormal glial cell morphology / MGI
- abnormal locus ceruleus morphology / MGI
- abnormal noradrenaline level / MGI
- abnormal brain interneuron morphology / MGI
- abnormal area postrema morphology / MGI
- absent facial nerve / MGI
- abnormal neuron physiology / MGI
- abnormal neuronal precursor proliferation / MGI
- decreased neuronal precursor cell number / MGI
- abnormal ciliary ganglion morphology / MGI
- decreased pulmonary ventilation / MGI
- impaired pupillary reflex / MGI
- neonatal lethality, complete penetrance / MGI
- embryonic lethality during organogenesis, complete penetrance / MGI
- lethality throughout fetal growth and development, complete penetrance / MGI
- embryonic lethality during organogenesis, incomplete penetrance / MGI
- preweaning lethality, incomplete penetrance / MGI
- abnormal retrotrapezoid nucleus morphology / MGI
- impaired neuron differentiation / MGI
- decreased enteric neural crest cell number / MGI
- decreased enteric neural crest cell proliferation / MGI
- abnormal enteric neural crest cell migration / MGI
C3HeB/FeJ-Phox2bm1Mhda/Ieg
| Status | Available to order |
| EMMA ID | EM:10207 |
| Citation information | RRID:IMSR_EM:10207 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-Phox2bm1Mhda/Ieg |
| Alternative name | C3HeB/FeJ-Phox2bD32AMhda (internal lab code Phox-01) |
| Strain type | Induced Mutant Strains : Chemically-induced |
| Allele/Transgene symbol | Phox2bm1Mhda |
| Gene/Transgene symbol | Phox2b |
Information from provider
| Provider | Martin Hrabe de Angelis |
| Provider affiliation | Institute of Experimental Genetics, Helmholtz Zentrum München |
| Genetic information | Exon 1 c.95 T-to-G, p.Asp32Ala PROVEAN prediction:-4.16 (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 | not known |
| 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 | heterozygous C3H males |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Haddad syndrome / Orphanet_99803
- Ondine syndrome / Orphanet_661
MGI phenotypes (gene matching)
Information on how we integrate external resources can be found here
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