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Symbol
Name
ID
Six1
sine oculis-related homeobox 1
MGI:102780
Phenotype annotations related to craniofacial
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
Availability Mouse Genotype
Six1Cwe/Six1Cwe
Six1em1(IMPC)Mbp/Six1em1(IMPC)Mbp
Six1tm1Kwk/Six1tm1Kwk
Six1tm1Mair/Six1tm1Mair
Six1tm1Rsd/Six1tm1Rsd
Six1tm1Mair/Six1+

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
05/21/2024
MGI 6.23
The Jackson Laboratory