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Symbol Name ID |
Hprt hypoxanthine guanine phosphoribosyl transferase MGI:96217 |
Allele Symbol
Name Chr Synonyms Category Phenotypic Classes Human Diseases
Hprtb-m3
hypoxanthine guanine phosphoribosyl transferase; hypoxanthine guanine phosphoribosyl transferase B, mutation 3 X Spontaneous behavior, nervous system Lesch-Nyhan Syndrome; LNS 300322
Hprttm1(Camk2a-APP*Swe*Lon,-MAPT*P301L*R406W)Geno
hypoxanthine guanine phosphoribosyl transferase; targeted mutation 1, Genoway X PLB1 Targeted (knock-in)
Hprttm1(cre)Mnn
hypoxanthine guanine phosphoribosyl transferase; targeted mutation 1, Jeffrey R Mann
X Hprt1tm1(cre)Mnn, hprt-cre, Hprtcre, Hprttm1(CAG.cre)MdCoh Targeted (knock-in) cardiovascular, craniofacial, embryogenesis, growth/size, mortality/aging, nervous system Focal Dermal Hypoplasia; FDH 305600
Hprttm1(Pck1-cre)Vhh
hypoxanthine guanine phosphoribosyl transferase; targeted mutation 1, Volker H Haase X PEPCK-Cre Targeted (knock-in) cardiovascular, cellular, hematopoietic, homeostasis, immune, liver/biliary, muscle, renal/urinary, tumorigenesis Von Hippel-Lindau Syndrome; VHL 193300
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
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last database update 06/05/2013 MGI 5.13 |
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