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Symbol
Name
ID
Ghr
growth hormone receptor
MGI:95708
Phenotype annotations related to skeleton
Darker colors indicate more annotations
Human Phenotypes
Limb undergrowth
Short long bone
Abnormal joint morphology
Delayed skeletal maturation
Disease(s) Associated with GHR
Laron syndrome

Mouse Phenotypes
short femur
short tibia
abnormal long bone epiphyseal plate morphology
abnormal long bone epiphyseal plate proliferative zone
abnormal long bone hypertrophic chondrocyte zone
decreased width of hypertrophic chondrocyte zone
decreased length of long bones
decreased bone mineral content
decreased areal bone mineral density
decreased bone mineral density
abnormal compact bone morphology
abnormal trabecular bone morphology
abnormal chondrocyte morphology
abnormal skeleton development
abnormal bone ossification
delayed endochondral bone ossification
Availability Mouse Genotype
Ghrtm1.1Jero/Ghrtm1.1Jero
Ghrtm1Arge/Ghrtm1Arge
Ghrtm1Jjk/Ghrtm1Jjk
Ghrtm1.1Masp/Ghrtm1.1Masp
Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+  (conditional)

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
08/06/2019
MGI 6.14
The Jackson Laboratory