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Symbol
Name
ID
Prkar1a
protein kinase, cAMP dependent regulatory, type I, alpha
MGI:104878
Phenotype annotations related to craniofacial
*Aspects of the system are reported to show a normal phenotype.
Darker colors indicate more annotations
Human Phenotypes
Frontal bossing
Brachycephaly
Calvarial hyperostosis
Mandibular prognathia
Trismus
Hypoplasia of the maxilla
Paranasal sinus neoplasm
Malar flattening
Flat face
Moon facies
Round face
Midface retrusion
Prominent forehead
Abnormal hard palate morphology
Tongue nodules
Open mouth
Hypodontia
Delayed eruption of teeth
Dental malocclusion
Open bite
Palatine myxoma
Anteverted nares
Depressed nasal ridge
Broad nasal tip
Depressed nasal bridge
Wide nasal bridge
Short nose
Neoplasm of the pharynx
Epicanthus
Nodular changes affecting the eyelids
Telecanthus
Disease(s) Associated with PRKAR1A
acrodysostosis
Carney complex
primary pigmented nodular adrenocortical disease

Mouse Phenotypes
craniofacial phenotype
abnormal craniofacial morphology
abnormal craniofacial bone morphology
abnormal nose morphology
short snout
increased facial tumor incidence
Availability Mouse Genotype
Prkar1atm1.1Geno/Prkar1a+
Prkar1atm1.2Lsk/Prkar1atm1.2Lsk
Tg(Tyr-cre)3Gfk/0  (conditional)
Prkar1atm2Gsm/Prkar1atm2Gsm
Tg(Plp1-cre)1Bzal/0  (conditional)
Prkar1atm2Gsm/Prkar1atm2Gsm
Tlx2tm1.1(cre)Rpk/Tlx2+  (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
04/16/2024
MGI 6.23
The Jackson Laboratory