- abnormal heart morphology / MGI
- decreased body size / MGI
- blepharoptosis / MGI
- postnatal growth retardation / MGI
- absent circulating adrenaline / MGI
- absent circulating noradrenaline / MGI
- increased circulating corticosterone level / MGI
- increased dopamine level / MGI
- abnormal glucose homeostasis / MGI
- increased circulating insulin level / MGI
- postnatal lethality / MGI
- premature death / MGI
- no abnormal phenotype detected / MGI
- decreased circulating glucagon level / MGI
- decreased glucagon secretion / MGI
- insulin resistance / MGI
- abnormal food intake / MGI
- decreased circulating glucose level / MGI
- embryonic lethality during organogenesis / MGI
- neonatal lethality, incomplete penetrance / MGI
- prenatal lethality, complete penetrance / MGI
- embryonic lethality during organogenesis, incomplete penetrance / MGI
C57BL/6-Dbhtm1a(EUCOMM)Wtsi/Cnbc
Status | Available to order |
EMMA ID | EM:12233 |
International strain name | C57BL/6-Dbhtm1a(EUCOMM)Wtsi/Cnbc |
Alternative name | Dbhtm1a(EUCOMM)Wtsi |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Dbhtm1a(EUCOMM)Wtsi |
Gene/Transgene symbol | Dbh |
Information from provider
Provider | Miguel Soares |
Provider affiliation | Biomedicine, LAIMM - Faculty of Medicine of Porto, Portugal |
Genetic information | Gene targeted: Dbh (dopamine beta hydroxylase; MGI:94864). Knockout first mice (KOMP tm1a allele; reporter-tagged insertion with conditional potential). |
Phenotypic information | Homozygous:http://www.informatics.jax.org/marker/phenotypes/MGI:94864Heterozygous:no abnormal phenotype detected |
Breeding history | 10+ generations. First backcrosses (not with parents but with unrelated C57BL/6J animals), then intercrosses (avoided consanguinity). |
References | None available |
Homozygous fertile | not known |
Homozygous viable | no |
Homozygous matings required | no |
Immunocompromised | no |
Information from EMMA
Archiving centre | CNB-CSIC, Centro Nacional de Biotecnologia, Madrid, Spain |
Animals used for archiving | heterozygous C57BL/6J |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Dopamine beta-hydroxylase deficiency / Orphanet_230
MGI phenotypes (gene matching)
Information on how we integrate external resources can be found here
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