About   Help   FAQ
Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Boc
BOC cell adhesion associated, oncogene regulated
MGI:2151153
39 phenotypes from multigenic genotypes
Export: Excel File
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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support. 		last database update
11/19/2024
MGI 6.24 		The Jackson Laboratory