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Symbol
Name
ID

Npr2
natriuretic peptide receptor 2
MGI:97372

Phenotype annotations related to nervous system

*	Aspects of the system are reported to show a normal phenotype.
	Darker colors indicate more annotations

Human Phenotypes	Intellectual disability
Disease(s) Associated with NPR2	Intellectual disability
acromesomelic dysplasia, Maroteaux type

Mouse Phenotypes		nervous system phenotype	abnormal sensory neuron innervation pattern	abnormal cranial nerve morphology	abnormal trigeminal nerve morphology	abnormal dorsal root ganglion morphology	abnormal spinal cord dorsal column morphology
Availability	Mouse Genotype	nervous system phenotype	abnormal sensory neuron innervation pattern	abnormal cranial nerve morphology	abnormal trigeminal nerve morphology	abnormal dorsal root ganglion morphology	abnormal spinal cord dorsal column morphology
	Npr2^cn/Npr2^cn
	Npr2^tm1Fgr/Npr2^tm1Fgr
	Npr2^{tm2.1(cre/ERT2)Fgr}/Npr2^cn Tg(CAG-Bgeo/ALPP)1Lbe/0	*

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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