C57BL/6N-Avptm1a(EUCOMM)Wtsi/H
Status | Available to order |
EMMA ID | EM:07776 |
International strain name | C57BL/6N-Avptm1a(EUCOMM)Wtsi/H |
Alternative name | EPD0339_3_H07 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Avptm1a(EUCOMM)Wtsi |
Gene/Transgene symbol | Avp |
Disclaimer | Please note that for EUCOMM and KOMP-CSD mice supplied to the scientific community by INFRAFRONTIER/EMMA:
|
Information from provider
Provider | MRC, Medical Research Council |
Provider affiliation | Mary Lyon Centre at MRC Harwell |
Genetic information | This mouse line originates from EUCOMM ES clone EPD0339_3_H07. For further details on the construction of this clone see the page at the IMPC portal. |
Phenotypic information | Potential phenotyping data in the IMPC portal |
References | None available |
Information from EMMA
Archiving centre | Mary Lyon Centre at MRC Harwell, Oxford, United Kingdom |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Hereditary central diabetes insipidus / Orphanet_30925
- Familial cold urticaria / Orphanet_47045
- Muckle-Wells syndrome / Orphanet_575
- CINCA syndrome / Orphanet_1451
IMPC phenotypes (gene matching)
MGI phenotypes (gene matching)
- abnormal hypothalamus morphology / MGI
- dehydration / MGI
- polyuria / MGI
- no abnormal phenotype detected / MGI
- decreased urine osmolality / MGI
- no phenotypic analysis / MGI
- abnormal hormone level / MGI
- abnormal circulating hormone level / MGI
- abnormal hypothalamus physiology / MGI
- abnormal supraoptic nucleus morphology / MGI
- postnatal lethality, complete penetrance / MGI
- increased fluid intake / MGI
Information on how we integrate external resources can be found here
INFRAFRONTIER® and European Mouse Mutant Archive - EMMA® are registered trademarks at the European Union Intellectual Property Office (EUIPO).