Symbol Name ID |
Six1
sine oculis-related homeobox 1 MGI:102780 |
Darker colors indicate more annotations |
Human Phenotypes | Preauricular pit |
Disease(s) Associated with SIX1 | |
autosomal dominant nonsyndromic deafness 23 |
Mouse Phenotypes | abnormal craniofacial morphology |
abnormal craniofacial bone morphology |
abnormal styloid process morphology |
abnormal Meckel's cartilage morphology |
abnormal frontal bone morphology |
short temporal bone squamous part |
abnormal hyoid bone greater horn morphology |
short mandible |
short maxilla |
micrognathia |
abnormal nasal bone morphology |
absent turbinates |
short zygomatic bone |
abnormal incus morphology |
absent incus |
abnormal malleus morphology |
abnormal stapes morphology |
absent stapes |
abnormal face development |
abnormal midface morphology |
abnormal genioglossus muscle morphology |
decreased tongue size |
abnormal nose morphology |
abnormal external nares morphology |
abnormal nasal cavity morphology |
absent vomeronasal organ |
abnormal olfactory epithelium morphology |
absent olfactory epithelium |
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Availability | Mouse Genotype | ||||||||||||||||||||||||||||
Six1Cwe/Six1Cwe | |||||||||||||||||||||||||||||
Six1em1(IMPC)Mbp/Six1em1(IMPC)Mbp | |||||||||||||||||||||||||||||
Six1tm1Kwk/Six1tm1Kwk | |||||||||||||||||||||||||||||
Six1tm1Mair/Six1tm1Mair | |||||||||||||||||||||||||||||
Six1tm1Rsd/Six1tm1Rsd | |||||||||||||||||||||||||||||
Six1tm1Mair/Six1+ |
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 05/21/2024 MGI 6.23 |
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