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Symbol
Name
ID
Prkg2
protein kinase, cGMP-dependent, type II
MGI:108173
Phenotype annotations related to skeleton
*Aspects of the system are reported to show a normal phenotype.
Darker colors indicate more annotations
Human Phenotypes
Mandibular prognathia
Prominent deltoid tuberosities
Radial bowing
Ulnar bowing
Genu valgum
Genu varum
Short phalanx of finger
Short finger
Broad finger
Short toe
Broad toe
Sandal gap
Broad phalanx
Short metatarsal
Metaphyseal irregularity
Flared metaphysis
Short metacarpal
Mesomelia
Rhizomelia
Accelerated skeletal maturation
Enlargement of the costochondral junction
Prominent sternum
Thoracic scoliosis
Lumbar hyperlordosis
Beaking of vertebral bodies
Platyspondyly
Thoracic platyspondyly
Disease(s) Associated with PRKG2
acromesomelic dysplasia-4

Mouse Phenotypes
skeleton phenotype
abnormal cranium morphology
short humerus
short ulna
short femur
short tibia
abnormal long bone hypertrophic chondrocyte zone
small vertebrae
abnormal bone ossification
Availability Mouse Genotype
Prkg2tm1Pfe/Prkg2tm1Pfe *

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