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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Br
brachyrrhine
MGI:88189
40 phenotypes from 1 allele in 1 genetic background
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Allelic Composition
Genetic Background
Annotated Term Reference
Br/Br+
involves: 101/H * C3H/HeH
abnormal basicranium morphology J:15489
abnormal craniofacial bone morphology J:15489
abnormal kidney morphology J:13450
abnormal mandibular coronoid process morphology J:15489
abnormal neurocranium morphology J:15489
abnormal tooth wear J:15489
absent kidney cortex J:71108
decreased body size J:13450
decreased palatal length J:15489
kidney cyst J:71108
long incisors J:15489
malocclusion J:15489
midface hypoplasia J:15489, J:47869
midline cleft upper lip J:13450, J:47869
pale kidney J:13450
premature death J:13450
short mandibular coronoid process J:15489
short premaxilla J:15489
short snout J:13450
small kidney J:13450
small mandible J:15489
small mandibular condyloid process J:15489
small mandibular coronoid process J:15489
Br/Br
involves: 101/H * C3H/HeH
abnormal kidney cortex morphology J:71108
abnormal kidney development J:71108
abnormal kidney vasculature morphology J:71108
abnormal nephron morphology J:71108
abnormal secondary palate development J:47869
cleft secondary palate J:47869
decreased palatal shelf size J:47869
dilated proximal convoluted tubule J:71108
dilated renal tubule J:71108
failure of palatal shelf elevation J:47869
kidney cyst J:71108
midface hypoplasia J:47869
midline facial cleft J:47869
neonatal lethality, complete penetrance J:47869
palatal shelves fail to meet at midline J:47869
perinatal lethality, complete penetrance J:71108
persistence of medial edge epithelium during palatal shelf fusion J:47869
polycystic kidney J:71108
renal hypoplasia J:71108

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
11/12/2024
MGI 6.24
The Jackson Laboratory