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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Ankrd11
ankyrin repeat domain 11
MGI:1924337
79 phenotypes from 3 alleles in 3 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Ankrd11tm1b(EUCOMM)Wtsi/Ankrd11+
C57BL/6N-Ankrd11tm1b(EUCOMM)Wtsi/Ics
abnormal auditory brainstem response J:211773
abnormal startle reflex J:211773
abnormal vitreous body morphology J:211773
decreased body length J:211773
decreased prepulse inhibition J:211773
decreased startle reflex J:211773
increased circulating cholesterol level J:211773
increased circulating HDL cholesterol level J:211773
Ankrd11tm1b(EUCOMM)Wtsi/Ankrd11tm1b(EUCOMM)Wtsi
C57BL/6N-Ankrd11tm1b(EUCOMM)Wtsi/Ics
abnormal embryo development J:211773
preweaning lethality, complete penetrance J:211773
Ankrd11tm1c(EUCOMM)Wtsi/Ankrd11+
E2f1Tg(Wnt1-cre)2Sor/E2f1+
involves: C3H * C57BL/6 * C57BL/6N
abnormal frontal bone morphology J:306391
abnormal mandible morphology J:306391
abnormal midface morphology J:306391
abnormal neurocranium morphology J:306391
abnormal nose morphology J:306391
abnormal pterygoid bone morphology J:306391
enlarged neurocranium J:306391
large anterior fontanelle J:306391
midface hypoplasia J:306391
normal mortality/aging J:306391
narrow face J:306391
wide metopic suture J:306391
Ankrd11tm1c(EUCOMM)Wtsi/Ankrd11tm1c(EUCOMM)Wtsi
E2f1Tg(Wnt1-cre)2Sor/E2f1+
involves: C3H * C57BL/6 * C57BL/6N
abnormal basicranium morphology J:306391
abnormal bone collagen fibril morphology J:306391
abnormal bone remodeling J:306391
abnormal cranial blood vasculature morphology J:306391
abnormal craniofacial morphology J:306391
abnormal head morphology J:306391
abnormal intramembranous bone ossification J:306391
abnormal neurocranium morphology J:306391
abnormal osteocyte morphology J:306391
abnormal palatal mesenchymal cell proliferation J:306391
abnormal palatal shelf morphology J:306391
abnormal palatine bone morphology J:306391
abnormal snout skin morphology J:306391
absent pterygoid process J:306391
cleft hard palate J:306391
cleft palate J:306391
decreased bone ossification J:306391
decreased bone resorption J:306391
decreased bone trabecula number J:306391
decreased osteoclast cell number J:306391
decreased tongue size J:306391
delayed intramembranous bone ossification J:306391
domed cranium J:306391
eyelids open at birth J:306391
frontal bone hypoplasia J:306391
hypopigmentation J:306391
impaired ossification of basisphenoid bone J:306391
large anterior fontanelle J:306391
micrognathia J:306391
midface hypoplasia J:306391
palatal shelf hypoplasia J:306391
palatal shelves fail to meet at midline J:306391
perinatal lethality, complete penetrance J:306391
retrognathia J:306391
short tongue J:306391
small frontal bone J:306391
small mandible J:306391
small parietal bone J:306391
tongue hypoplasia J:306391
triangular face J:306391
Ankrd11Yod/Ankrd11+
involves: BALB/cAnNCrl * C3H/HeH
abnormal bone structure J:136455
abnormal craniofacial bone morphology J:136455
abnormal frontonasal suture morphology J:136455
abnormal metopic suture morphology J:136455
abnormal nasal bone morphology J:136455
broad face J:136455
decreased body length J:136455
decreased body weight J:136455
decreased bone mass J:136455
decreased bone mineral density of femur J:136455
decreased circulating leptin level J:136455
decreased compact bone area J:136455
decreased osteoclast cell number J:136455
domed cranium J:136455
enlarged parietal bone J:136455
increased cranium width J:136455
kyphosis J:136455
short face J:136455
short frontal bone J:136455
short nasal bone J:136455
Ankrd11Yod/Ankrd11Yod
involves: BALB/cAnNCrl * C3H/HeH
decreased embryo size J:136455
embryonic lethality during organogenesis, complete penetrance J:136455
failure of initiation of embryo turning J:136455

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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
11/12/2024
MGI 6.24
The Jackson Laboratory