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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Cilk1
ciliogenesis associated kinase 1
MGI:1934157
57 phenotypes from 3 alleles in 3 genetic backgrounds
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Allelic Composition
Genetic Background		 Annotated Term Reference
Cilk1tm1.1Zfu/Cilk1tm1.1Zfu
B6.Cg-Cilk1tm1.1Zfu/Zfu 		abnormal branching involved in lung morphogenesis J:309653
abnormal cervical flexure morphology J:309376
abnormal chest morphology J:309376
abnormal chondrocyte differentiation J:309376
abnormal endochondral bone ossification J:309376
abnormal hindlimb morphology J:309376
abnormal intervertebral disk development J:309376
abnormal intervertebral disk morphology J:309376
abnormal long bone epiphyseal plate proliferative zone J:309376
abnormal long bone morphology J:309376
abnormal lung alveolus development J:309653
abnormal lung bud morphology J:309653
abnormal lung saccule morphology J:309653
abnormal lung-associated mesenchyme development J:309653
abnormal neck morphology J:309376
abnormal primary cilium morphology J:309653
abnormal tarsal bone morphology J:309376
abnormal thoracic cage morphology J:309376
abnormal vertebrae morphology J:309376
abnormal vertebral column morphology J:309376
abnormal vertebral transverse process morphology J:309376
absent nucleus pulposus J:309376
broad head J:309376
decreased bone mineralization J:309376
decreased bone ossification J:309376
decreased length of long bones J:309376
decreased mesenchymal cell proliferation involved in lung development J:309653
enhanced autophagy J:309653
increased mouth size J:309376
neonatal lethality, complete penetrance J:309653
polydactyly J:309376, J:309653
pulmonary hypoplasia J:309653
respiratory failure J:309653
short femur J:309376
short limbs J:309376, J:309653
short neck J:309376
small snout J:309376
thick lung-associated mesenchyme J:309653
Cilk1tm1a(KOMP)Mbp/Cilk1tm1a(KOMP)Mbp
C57BL/6N-Cilk1tm1a(KOMP)Mbp 		abnormal bone mineralization J:211652
abnormal digit development J:211652
abnormal kidney development J:211652
abnormal long bone morphology J:211652
abnormal primary cilium morphology J:211652
abnormal skeleton development J:211652
abnormal tongue morphology J:211652
abnormal ulna morphology J:211652
cleft palate J:211652
decreased length of long bones J:211652
decreased tongue size J:211652
delayed bone ossification J:211652
dilated brain ventricle J:211652
edema J:211652
hydrocephaly J:211652
lethality throughout fetal growth and development, complete penetrance J:211652
normal nervous system phenotype J:211652
preaxial polydactyly J:211652
short limbs J:211652
Cilk1tm1b(KOMP)Mbp/Cilk1tm1b(KOMP)Mbp
C57BL/6N-Cilk1tm1b(KOMP)Mbp/Ucd 		abnormal heart morphology J:211773
enlarged heart J:211773
increased basophil cell number J:211773
increased neutrophil cell number J:211773
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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Send questions and comments to User Support. 		last database update
11/05/2024
MGI 6.24 		The Jackson Laboratory