- 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 |
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/6N Tac |
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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