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Symbol
Name
ID
Prrx1
paired related homeobox 1
MGI:97712
Phenotype annotations related to skeleton
Darker colors indicate more annotations
Human Phenotypes
Mandibular aplasia
Micrognathia
Disease(s) Associated with PRRX1
agnathia-otocephaly complex

Mouse Phenotypes
abnormal cranium morphology
abnormal Meckel's cartilage morphology
absent supraoccipital bone
absent alisphenoid bone
alisphenoid bone hypoplasia
pterygoid bone hypoplasia
absent temporal bone squamous part
abnormal mandible morphology
absent temporomandibular joint
mandible hypoplasia
absent maxillary shelf
maxillary shelf hypoplasia
absent palatine bone horizontal plate
absent zygomatic bone
abnormal middle ear ossicle morphology
abnormal incus morphology
abnormal malleus morphology
absent gonial bone
abnormal malleus manubrium morphology
short malleus manubrium
abnormal malleus processus brevis morphology
abnormal stapes morphology
abnormal stapes crus morpholgy
absent stapes obturator foramen
bowed radius
short radius
short ulna
short fibula
abnormal tibia morphology
bowed tibia
short tibia
abnormal metacarpal bone morphology
abnormal long bone morphology
abnormal long bone hypertrophic chondrocyte zone
decreased width of hypertrophic chondrocyte zone
abnormal thoracic vertebrae morphology
abnormal vertebrae morphology
abnormal trabecular bone morphology
abnormal cartilage morphology
abnormal incudostapedial joint morphology
abnormal stylohyoid ligament morphology
delayed bone ossification
Availability Mouse Genotype
Prrx1tm1Bhr/Prrx1tm1Bhr
Prrx1tm1Tex/Prrx1tm1Tex
Prrx1tm1Jfm/Prrx1tm1Tex

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