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Symbol
Name
ID
Gli2
GLI-Kruppel family member GLI2
MGI:95728
Phenotype annotations related to skeleton
Darker colors indicate more annotations
Human Phenotypes
Hypoplasia of the premaxilla
Hypoplasia of the maxilla
Malar flattening
Microcephaly
Wide anterior fontanel
Short neck
Postaxial hand polydactyly
Postaxial polydactyly
Disease(s) Associated with GLI2
Culler-Jones syndrome
holoprosencephaly 9

Mouse Phenotypes
abnormal basioccipital bone morphology
abnormal basisphenoid bone morphology
abnormal frontal bone morphology
abnormal parietal bone morphology
absent presphenoid bone
absent lower incisors
absent upper incisors
small mandibular condyloid process
absent temporomandibular joint disk
small mandible
absent maxillary shelf
short maxilla
absent palatine bone horizontal plate
short humerus
bowed radius
short radius
short ulna
short femur
short fibula
short tibia
abnormal tracheal cartilage morphology
abnormal long bone morphology
short sternum
increased rib number
absent intervertebral disk
abnormal spine curvature
abnormal vertebral body morphology
decreased chondrocyte number
abnormal epiphyseal plate morphology
delayed bone ossification
Availability Mouse Genotype
Gli2tm1Alj/Gli2tm1Alj

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
04/09/2024
MGI 6.23
The Jackson Laboratory