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Symbol Name ID |
Prrx1
paired related homeobox 1 MGI:97712 |
| Darker colors indicate more annotations |
| Human Phenotypes | Mandibular aplasia |
Micrognathia |
Cleft palate |
Aglossia |
Microglossia |
Narrow mouth |
Absent nares |
Aplasia/Hypoplasia involving the nose |
Wide nose |
Aplasia/Hypoplasia of the eyebrow |
Downslanted palpebral fissures |
| 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 |
abnormal palatal shelf fusion at midline |
cleft secondary palate |
pointed snout |
lowered ear position |
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| Availability | Mouse Genotype | ||||||||||||||||||||||||||||
| 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 04/16/2024 MGI 6.23 |
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