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Symbol Name ID |
Prrx1
paired related homeobox 1 MGI:97712 |
| Darker colors indicate more annotations |
| Human Phenotypes | Narrow internal auditory canal |
Conductive hearing impairment |
Low-set ears |
Low-set, posteriorly rotated ears |
Synotia |
| Disease(s) Associated with PRRX1 | |||||
| agnathia-otocephaly complex |
| Mouse Phenotypes | 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 |
lowered ear position |
small otic capsule |
absent tympanic ring |
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| Availability | Mouse Genotype | |||||||||||||
| Prrx1tm1Tex/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 04/30/2024 MGI 6.23 |
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