Symbol Name ID |
Prrx1
paired related homeobox 1 MGI:97712 |
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 |
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Availability | Mouse Genotype | ||||||||||||||||||||||||||||||||||||||||||
Prrx1tm1Bhr/Prrx1tm1Bhr | |||||||||||||||||||||||||||||||||||||||||||
Prrx1tm1Tex/Prrx1tm1Tex | |||||||||||||||||||||||||||||||||||||||||||
Prrx1tm1Jfm/Prrx1tm1Tex |
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 |
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