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Symbol
Name
ID
Npr2
natriuretic peptide receptor 2
MGI:97372
Phenotype annotations related to craniofacial
Darker colors indicate more annotations
Human Phenotypes
Frontal bossing
Dolichocephaly
Prominent forehead
Depressed nasal bridge
Short nose
Disease(s) Associated with NPR2
acromesomelic dysplasia, Maroteaux type

Mouse Phenotypes
abnormal craniofacial morphology
abnormal cranium morphology
abnormal basicranium morphology
decreased cranium length
decreased cranium width
abnormal neurocranium morphology
enlarged interparietal bone
small supraoccipital bone
enlarged parietal bone
long lower incisors
long upper incisors
long incisors
malocclusion
abnormal mandibular condyloid process morphology
short maxilla
small nasal bone
domed cranium
abnormal nose morphology
abnormal snout morphology
short snout
round head
Availability Mouse Genotype
Npr2cn-2J/Npr2cn-2J
Npr2cn-3J/Npr2cn-3J
Npr2cn/Npr2cn
Npr2em1(IMPC)H/Npr2em1(IMPC)H
Npr2slw/Npr2slw
Npr2tm1Gar/Npr2tm1Gar
Npr2em1(IMPC)H/Npr2+
Tg(Col11a2-Npr2*)28Keoz/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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last database update
04/16/2024
MGI 6.23
The Jackson Laboratory