- decreased total retina thickness / IMPC
- embryonic lethality prior to organogenesis / IMPC
- embryonic lethality prior to tooth bud stage / IMPC
- preweaning lethality, complete penetrance / IMPC
- decreased erythrocyte cell number / IMPC
- abnormal retina outer nuclear layer morphology / IMPC
- increased prepulse inhibition / IMPC
- thick ventricular wall / IMPC
C57BL/6N-Atm1Brd Yipf5tm1a(EUCOMM)Hmgu/IcsOrl
Status | Available to order |
EMMA ID | EM:07695 |
International strain name | C57BL/6N-Atm1Brd Yipf5tm1a(EUCOMM)Hmgu/IcsOrl |
Alternative name | HEPD0534_4_D04 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Yipf5tm1a(EUCOMM)Hmgu |
Gene/Transgene symbol | Yipf5 |
Disclaimer | Please note that for EUCOMM and KOMP-CSD mice supplied to the scientific community by INFRAFRONTIER/EMMA:
|
Information from provider
Provider | ICS, Institut Clinique de la Souris |
Provider affiliation | ICS, Institut Clinique de la Souris |
Genetic information | This mouse line originates from EUCOMM ES clone HEPD0534_4_D04. 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 | Institut de Transgenose, INTRAGENE, Orléans, France |
Animals used for archiving | heterozygous C57BL/6N Tac, wild-type C57BL/6N Tac |
Stage of embryos | 2-cell |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Primary microcephaly-epilepsy-permanent neonatal diabetes syndrome / Orphanet_306558
IMPC phenotypes (gene matching)
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).