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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Rfng
RFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase
MGI:894275
7 phenotypes from 3 alleles in 4 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Rfngtm1Grid/Rfngtm1Grid
involves: 129S1/Sv * C57BL/6J
no abnormal phenotype detected J:77247
Rfngtm2.1Tfv/Rfngtm2.1Tfv
involves: 129P2/OlaHsd * 129S6/SvEvTac
no abnormal phenotype detected J:110952
Rfngtm2.1Tfv/Rfngtm2.1Tfv
involves: FVB/N
no abnormal phenotype detected J:110952
Rfngtm2Tfv/Rfngtm2Tfv
involves: 129P2/OlaHsd * 129S6/SvEvTac
perinatal lethality, complete penetrance J:110952
Rfngtm2Tfv/Rfngtm2Tfv
involves: 129P2/OlaHsd * C57BL/6J
cleft secondary palate J:110952
failure of palatal shelf elevation J:110952
oligodactyly J:110952
perinatal lethality, complete penetrance J:110952
short mandible J:110952
syndactyly J:110952

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
04/30/2024
MGI 6.23
The Jackson Laboratory