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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Rr27
regulatory region 27
MGI:5489785
26 phenotypes from 18 alleles in 12 genetic backgrounds
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Allelic Composition
Genetic Background		 Annotated Term Reference
Rr27tm1.1Kpfe/Rr27+
involves: 129S1/Sv * 129X1/SvJ * FVB/N 		abnormal DNA methylation J:82798
Rr27tm1.1Mnn/Rr27+
involves: 129S1/Sv * CAST/Ei * FVB/NJ * Swiss 		abnormal imprinting J:308869
decreased birth body size J:308869
decreased embryo weight J:308869
normal mortality/aging J:308869
Rr27tm1.1Msb/Rr27+
involves: 129P2/OlaHsd * C57BL/6J 		abnormal imprinting J:52162, J:105567, J:106218
decreased body weight J:52162
increased body size J:52162
Rr27tm1Kpfe/Rr27+
Tg(Tpbpa-cre,-EGFP)5Jcc/0
involves: 129S1/Sv * 129X1/SvJ 		abnormal maternal decidual layer morphology J:325552
abnormal placenta junctional zone morphology J:325552
abnormal trophoblast giant cell morphology J:325552
decreased placental labyrinth size J:325552
normal embryo phenotype J:325552
normal growth/size/body region phenotype J:325552
increased spongiotrophoblast cell number J:325552
Rr27tm1Kpfe/Rr27tm1Kpfe
Tg(CD2-cre)1Sriv/?
involves: 129S1/Sv * 129X1/SvJ 		normal cellular phenotype J:82595
Rr27tm1Kpfe/Rr27tm1Kpfe
Tg(Ckmm-cre)5Khn/0
involves: 129S1/Sv * 129X1/SvJ * FVB 		abnormal imprinting J:82798
Rr27tm1Pes/Rr27+
involves: 129S1/SvImJ * FVB/N-Chr 7CAST/Ei/J 		increased fetal weight J:91020
increased placenta weight J:91020
paternal imprinting J:91020
polydactyly J:91020
Rr27tm1Rohl/Rr27+
involves: 129S1/Sv * 129X1/SvJ 		abnormal crypts of Lieberkuhn morphology J:97083
Rr27tm1Rohl/Rr27+
involves: 129S1/Sv * 129X1/SvJ * FVB/N * SD7 		abnormal imprinting J:82427
increased susceptibility to weight gain J:82427
Rr27tm1Tilg/Rr27+
involves: 129S1/Sv 		abnormal imprinting J:81888
increased body weight J:81888
Rr27tm1Wrk/Rr27+
Not Specified 		no abnormal phenotype detected J:91713
Rr27tm2.1Pes/Rr27+
involves: 129S1/Sv * 129S1/SvImJ * CAST/Ei * FVB/NJ 		normal cellular phenotype J:195982
Rr27tm2Msb/Rr27+
Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+
involves: 129P2/OlaHsd * C57BL/6 * DBA 		paternal imprinting J:105567
Rr27tm2Rohl/Rr27tm2Rohl
Not Specified 		no abnormal phenotype detected J:89915
Rr27tm2Tilg/Rr27+
involves: 129S1/Sv 		normal cellular phenotype J:86440
Rr27tm2Wrk/Rr27+
involves: 129P2/OlaHsd * C57BL/6J 		no abnormal phenotype detected J:91593
Rr27tm3Msb/Rr27+
involves: 129P2/OlaHsd * C57BL/6J 		abnormal imprinting J:106218
Rr27tm4Msb/Rr27+
involves: 129P2/OlaHsd * C57BL/6J 		abnormal imprinting J:106218
increased embryo weight J:105567
increased placenta weight J:105567
Rr27tm5.1Msb/Rr27+
involves: 129P2/OlaHsd * C57BL/6 * M. m. castaneus 		abnormal imprinting J:173610
normal growth/size/body region phenotype J:173610
Rr27tm6.1Msb/Rr27+
involves: 129P2/OlaHsd * C57BL/6 * M. m. castaneus 		abnormal imprinting J:173610
normal growth/size/body region phenotype J:173610
Rr27tm7.1Msb/Rr27+
involves: 129P2/OlaHsd * C57BL/6 * M. m. castaneus 		increased birth weight J:211399
increased tongue size J:211399
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
12/10/2024
MGI 6.24 		The Jackson Laboratory