- 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
STOCK Ankrd11tm1a(EUCOMM)Wtsi/IcsOrl
Status | Available to order |
EMMA ID | EM:07651 |
Citation information | RRID:IMSR_EM:07651 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 Ankrd11tm1a(EUCOMM)Wtsi/IcsOrl |
Alternative name | EPD0678_1_F03 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Ankrd11tm1a(EUCOMM)Wtsi |
Gene/Transgene symbol | Ankrd11 |
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 mouse line originates from EUCOMM ES clone EPD0678_1_F03. 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/6NTac males |
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
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