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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Crkl
v-crk avian sarcoma virus CT10 oncogene homolog-like
MGI:104686
61 phenotypes from 4 alleles in 6 genetic backgrounds
Export: Excel File
Allelic Composition
Genetic Background
Annotated Term Reference
Crklsnoopy/Crklsnoopy
involves: C3H/HeH * C57BL/6JAnu
abnormal eye development J:199856
abnormal forebrain morphology J:199856
absent mandible J:199856
cyclopia J:199856
holoprosencephaly J:199856
mandible hypoplasia J:199856
ocular hypotelorism J:199856
Crklsnoopy/Crklsnoopy
involves: C57BL/6JAnu
abnormal auditory bulla morphology J:251775
abnormal basisphenoid bone morphology J:251775
abnormal craniofacial morphology J:251775
abnormal mandible morphology J:251775
abnormal oral cavity morphology J:251775
abnormal palatal shelf morphology J:251775
abnormal palatine bone morphology J:251775
abnormal pharynx morphology J:251775
abnormal zygomatic arch morphology J:251775
absent mandible J:251775
absent tongue J:251775
anophthalmia J:251775
basisphenoid bone hypoplasia J:251775
cleft secondary palate J:251775
cyclopia J:251775
decreased mouth size J:251775
delayed palatal shelf elevation J:251775
holoprosencephaly J:251775
increased palatal shelf size J:251775
mandible hypoplasia J:251775
maxilla hypoplasia J:251775
microphthalmia J:251775
premaxilla hypoplasia J:251775
proboscis J:251775
tongue hypoplasia J:251775
Crkltm1Cur/Crkltm1Cur
Tg(Nes-cre)1Kln/0
involves: 129S/SvEv * C57BL/6 * SJL
decreased body weight J:143049
normal nervous system phenotype J:143049
postnatal growth retardation J:143049
Crkltm1Hkp/Crkltm1Hkp
involves: 129S1/Sv * 129X1/SvJ
abnormal heart morphology J:76680
abnormal liver morphology J:76680
abnormal placenta morphology J:76680
embryonic lethality, complete penetrance J:76680
Crkltm1Hkp/Crkltm1Hkp
involves: 129S1/Sv * 129X1/SvJ * Black Swiss
abnormal caudal vertebrae morphology J:76680
decreased body weight J:76680
kinked tail J:76680
postnatal lethality, incomplete penetrance J:76680
ventricular septal defect J:76680
Crkltm1Imo/Crkltm1Imo
involves: 129S4/SvJaeSor * C57BL/6J
aberrant origin of the right subclavian artery J:67826
abnormal aortic arch morphology J:67826
abnormal cranial ganglia morphology J:67826
abnormal craniofacial morphology J:67826
abnormal glossopharyngeal ganglion morphology J:67826
abnormal heart left atrium morphology J:67826
abnormal nasal bone morphology J:67826
abnormal parathyroid gland development J:67826
abnormal thymus development J:67826
abnormal thyroid gland development J:67826
abnormal trigeminal ganglion morphology J:67826
abnormal vagus ganglion morphology J:67826
decreased body weight J:67826
decreased cranium height J:67826
dilated heart right atrium J:67826
double outlet right ventricle J:67826
increased cranium width J:67826
interrupted aortic arch J:67826
lethality throughout fetal growth and development, complete penetrance J:67826
ocular hypertelorism J:67826
otic hypertelorism J:67826
overriding aortic valve J:67826
pallor J:67826
short frontal bone J:67826
ventricular septal defect J:67826

Contributing Projects:
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
04/09/2024
MGI 6.23
The Jackson Laboratory