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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Boc
BOC cell adhesion associated, oncogene regulated
MGI:2151153
39 phenotypes from multigenic genotypes
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Allelic Composition
Genetic Background		 Annotated Term Reference
Boctm1Aok/Boc+
Gas1tm2Fan/Gas1+
involves: 129 * C57BL/6 * CD-1 		normal craniofacial phenotype J:310333
Boctm1Aok/Boc+
Gas1tm2Fan/Gas1tm2Fan
involves: 129 * C57BL/6 * CD-1 		abnormal palatal mesenchymal cell proliferation J:310333
abnormal secondary palate development J:310333
cleft palate J:310333
holoprosencephaly J:310333
Boctm1Aok/Boctm1Aok
Gas1tm2Fan/Gas1tm2Fan
involves: 129 * C57BL/6 * CD-1 		abnormal palatal mesenchymal cell proliferation J:310333
abnormal secondary palate development J:310333
abnormal vomeronasal organ morphology J:310333
bifid tongue J:310333
cleft palate J:310333
cleft secondary palate J:310333
failure of palatal shelf elevation J:310333
Boctm1Rsk/Boc+
Cdontm1Rsk/Cdontm1Rsk
involves: 129/Sv * 129S6/SvEvTac 		abnormal craniofacial development J:171767
abnormal craniofacial morphology J:171767
abnormal maxilla morphology J:171767
abnormal maxillary shelf morphology J:171767
abnormal palate development J:171767
abnormal premaxilla morphology J:171767
abnormal primary palate development J:171767
abnormal secondary palate development J:171767
abnormal upper lip morphology J:171767
absent maxillary shelf J:171767
absent primary palate J:171767
basisphenoid bone foramen J:171767
cleft palate J:171767
decreased maxillary shelf size J:171767
external nares atresia J:171767
holoprosencephaly J:171767
preweaning lethality, incomplete penetrance J:171767
small basisphenoid bone J:171767
Boctm1Rsk/Boctm1Rsk
Cdontm1Rsk/Cdontm1Rsk
B6.129-Boctm1Rsk Cdontm1Rsk 		cleft upper lip J:171767
normal craniofacial phenotype J:171767
holoprosencephaly J:171767
normal limbs/digits/tail phenotype J:171767
ocular hypotelorism J:171767
proboscis J:171767
Boctm1Rsk/Boctm1Rsk
Cdontm1Rsk/Cdontm1Rsk
involves: 129/Sv * 129S6/SvEvTac 		abnormal craniofacial development J:171767
abnormal external nares morphology J:171767
abnormal forebrain development J:171767
abnormal forebrain morphology J:171767
abnormal intervertebral disk development J:171767
abnormal lateral ganglionic eminence morphology J:171767
abnormal maxilla morphology J:171767
abnormal maxillary shelf morphology J:171767
abnormal medial ganglionic eminence morphology J:171767
abnormal nasal septum morphology J:171767
abnormal palatal shelf fusion at midline J:171767
abnormal palate development J:171767
abnormal premaxilla morphology J:171767
abnormal primary palate development J:171767
abnormal secondary palate development J:171767
abnormal upper lip morphology J:171767
absent maxillary shelf J:171767
absent primary palate J:171767
basisphenoid bone foramen J:171767
cleft palate J:171767
decreased maxillary shelf size J:171767
external nares atresia J:171767
failure of palatal shelf elevation J:171767
holoprosencephaly J:171767
lethality during fetal growth through weaning, complete penetrance J:171767
lobar holoprosencephaly J:171767
ocular hypotelorism J:171767
normal skeleton phenotype J:171767
small basisphenoid bone J:171767
Boctm2Rsk/Boc+
Cdontm1Rsk/Cdontm1Rsk
involves: 129/Sv * 129S6/SvEvTac 		abnormal craniofacial development J:171767
abnormal craniofacial morphology J:171767
abnormal maxilla morphology J:171767
abnormal maxillary shelf morphology J:171767
abnormal palate development J:171767
abnormal premaxilla morphology J:171767
abnormal primary palate development J:171767
abnormal secondary palate development J:171767
abnormal upper lip morphology J:171767
absent maxillary shelf J:171767
absent primary palate J:171767
basisphenoid bone foramen J:171767
cleft palate J:171767
decreased maxillary shelf size J:171767
external nares atresia J:171767
holoprosencephaly J:171767
preweaning lethality, incomplete penetrance J:171767
small basisphenoid bone J:171767
Boctm2Rsk/Boctm2Rsk
Cdontm1Rsk/Cdontm1Rsk
B6.129-Boctm2Rsk Cdontm1Rsk 		cleft upper lip J:171767
normal craniofacial phenotype J:171767
holoprosencephaly J:171767
normal limbs/digits/tail phenotype J:171767
ocular hypotelorism J:171767
proboscis J:171767
Boctm2Rsk/Boctm2Rsk
Cdontm1Rsk/Cdontm1Rsk
involves: 129/Sv * 129S6/SvEvTac 		abnormal craniofacial development J:171767
abnormal external nares morphology J:171767
abnormal forebrain development J:171767
abnormal forebrain morphology J:171767
abnormal intervertebral disk development J:171767
abnormal lateral ganglionic eminence morphology J:171767
abnormal maxilla morphology J:171767
abnormal maxillary shelf morphology J:171767
abnormal medial ganglionic eminence morphology J:171767
abnormal nasal septum morphology J:171767
abnormal palatal shelf fusion at midline J:171767
abnormal palate development J:171767
abnormal premaxilla morphology J:171767
abnormal primary palate development J:171767
abnormal secondary palate development J:171767
abnormal upper lip morphology J:171767
absent maxillary shelf J:171767
absent primary palate J:171767
basisphenoid bone foramen J:171767
cleft palate J:171767
decreased maxillary shelf size J:171767
external nares atresia J:171767
failure of palatal shelf elevation J:171767
holoprosencephaly J:171767
lethality during fetal growth through weaning, complete penetrance J:171767
lobar holoprosencephaly J:171767
ocular hypotelorism J:171767
normal skeleton phenotype J:171767
small basisphenoid bone J:171767
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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04/30/2024
MGI 6.23 		The Jackson Laboratory