STOCK Pafah1b1tm1c(EUCOMM)Hmgu/Ics
Status | Available to order |
EMMA ID | EM:11256 |
Citation information | RRID:IMSR_EM:11256 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 | STOCK Pafah1b1tm1c(EUCOMM)Hmgu/Ics |
Alternative name | HEPD0602_6_E12 |
Strain type | Targeted Mutant Strains : Targeted Conditional |
Allele/Transgene symbol | Pafah1b1tm1c(EUCOMM)Hmgu |
Gene/Transgene symbol | Pafah1b1 |
Disclaimer | Please note that for EUCOMM and KOMP-CSD mice supplied to the scientific community by INFRAFRONTIER/EMMA:
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Information from provider
Provider | ICS, Institut Clinique de la Souris |
Provider affiliation | ICS, Institut Clinique de la Souris |
Genetic information | This line originates from EUCOMM ES clone HEPD0602_6_E12, after breeding with a Flp recombinase deleter line to convert the original targeted allele tm1a (knock-out first allele) into a conditional allele tm1c. 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 | ICS, Institut Clinique de la Souris, Illkirch-Graffenstaden, France |
Animals used for archiving | heterozygous C57BL/6N males |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Subcortical band heterotopia / Orphanet_99796
- Lissencephaly due to LIS1 mutation / Orphanet_95232
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