Symbol Name ID |
Hmgcs2
3-hydroxy-3-methylglutaryl-Coenzyme A synthase 2 MGI:101939 |
Allelic Composition Genetic Background |
Annotated Term | Reference |
Fgfr2tm3.1Lni/Fgfr2+ Hmgcs2em1Wilh/Hmgcs2em1Wilh involves: 129S1/Sv * 129X1/SvJ * C57BL/6 |
normal reproductive system phenotype | J:285178 |
Hmgcs2tm1.1Yil/Hmgcs2tm1.1Yil Lgr5tm3(cre/ERT2)Cle/Lgr5+ Gt(ROSA)26Sortm9(CAG-tdTomato)Hze/Gt(ROSA)26Sor+ involves: 129S6/SvEvTac * C3H * C57BL/6J * C57BL/6NCrl |
abnormal intestinal crypt stem cell physiology | J:280699 |
abnormal jejunal goblet cell morphology | J:280699 | |
abnormal jejunum crypts of Lieberkuhn morphology | J:280699 | |
abnormal response to radiation | J:280699 | |
enhanced intestine regeneration | J:280699 | |
impaired intestine regeneration | J:280699 | |
increased Paneth cell number | J:280699 |
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 03/25/2025 MGI 6.24 |
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