- decreased bone mineral density / IMPC
- decreased startle reflex / IMPC
- abnormal retina vasculature morphology / IMPC
- decreased lean body mass / IMPC
- increased circulating cholesterol level / IMPC
- increased total body fat amount / IMPC
- abnormal vitreous body morphology / IMPC
- abnormal response to new environment / IMPC
- decreased heart weight / IMPC
- abnormal auditory brainstem response / IMPC
- abnormal head morphology / IMPC
- abnormal startle reflex / IMPC
- increased bone mineral content / IMPC
- preweaning lethality, complete penetrance / IMPC
- decreased prepulse inhibition / IMPC
- decreased body length / IMPC
- abnormal embryo development / IMPC
- increased circulating HDL cholesterol level / IMPC
Ankrd11tm1c(EUCOMM)Wtsi/Ics
| Status | Available to order |
| EMMA ID | EM:16058 |
| Citation information | RRID:IMSR_EM:16058 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 | Ankrd11tm1c(EUCOMM)Wtsi/Ics |
| Alternative name | Ankrd11tm1c(EUCOMM)Wtsi/Ics |
| Strain type | Targeted Mutant Strains : Conditional mutation |
| Allele/Transgene symbol | Ankrd11tm1c(EUCOMM)Wtsi |
| Gene/Transgene symbol | Ankrd11 |
Information from provider
| Provider | ICS, Institut Clinique de la Souris |
| Provider affiliation | ICS, Institut Clinique de la Souris |
| Genetic information | "Conditional ready" (floxed) allele obtained from the line STOCK Ankrd11tm1a(EUCOMM)Wtsi/IcsOrl (EMMA strain EM:07651). The L1L2_Bact_P cassette was removed by flp-mediated recombination using a flpo deleter mouse line (MGI:5285396). |
| Phenotypic information | Homozygous:N/AHeterozygous:N/A |
| Breeding history | Line produced in C57BL/6N genetic background, 6 breedings steps, one with a CamKIIa-cre line with little C57BL/6J genetic background. Current background: C57BL/6J 1.5625%, C57BL/6N 98.4375% |
| References |
|
| Homozygous fertile | not known |
| Homozygous viable | not known |
| Homozygous matings required | no |
| Immunocompromised | no |
Information from EMMA
| Archiving centre | ICS, Institut Clinique de la Souris, Illkirch-Graffenstaden, France |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- KBG syndrome / Orphanet_2332
IMPC phenotypes (gene matching)
MGI phenotypes (gene matching)
- decreased bone mineral density / MGI
- abnormal nasal bone morphology / MGI
- kyphosis / MGI
- domed cranium / MGI
- increased cranium width / MGI
- decreased body length / MGI
- decreased body weight / MGI
- decreased embryo size / MGI
- abnormal craniofacial bone morphology / MGI
- abnormal bone structure / MGI
- abnormal metopic suture morphology / MGI
- decreased bone mass / MGI
- failure of initiation of embryo turning / MGI
- short frontal bone / MGI
- enlarged parietal bone / MGI
- short nasal bone / MGI
- decreased osteoclast cell number / MGI
- decreased circulating leptin level / MGI
- abnormal frontonasal suture morphology / MGI
- decreased compact bone area / MGI
- embryonic lethality during organogenesis, complete penetrance / MGI
- short face / MGI
- broad face / MGI
Literature references
- Large-Scale Functional Assessment of Genes Involved in Rare Diseases with Intellectual Disabilities Unravels Unique Developmental and Behaviour Profiles in Mouse Models.;Meziane Hamid, Birling Marie-Christine, Wendling Olivia, Leblanc Sophie, Dubos Aline, Selloum Mohammed, Pavlovic Guillaume, Sorg Tania, Kalscheuer Vera M, Billuart Pierre, Laumonnier Frédéric, Chelly Jamel, van Bokhoven Hans, Herault Yann, ;2022;Biomedicines;10;; 36551904
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