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Phenotypes Associated with This Genotype
Genotype
MGI:3812210
Allelic
Composition		 Shhtm1Chg/Shh+
Sulf1Gt(XM190)Byg/Sulf1Gt(XM190)Byg
Sulf2Gt(PST111)Byg/Sulf2Gt(PST111)Byg
Genetic
Background		 involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/10
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Shhtm1Chg mutation (2 available); any Shh mutation (48 available)
Sulf1Gt(XM190)Byg mutation (0 available); any Sulf1 mutation (112 available)
Sulf2Gt(PST111)Byg mutation (1 available); any Sulf2 mutation (177 available)
♀ phenotype observed in females
♂ phenotype observed in males
N normal phenotype
craniofacial
abnormal craniofacial morphology ( J:130163 )
• agnathic mice exhibit a narrow craniofacial region
absent mandible ( J:130163 )
• in 3 of 126 mice age E14.5 to E18.5
short mandible ( J:130163 )
• in 2 of 126 mice age E14.5 to E18.5

vision/eye
microphthalmia ( J:130163 )
• agnathic mice exhibit small or absent eyes
anophthalmia ( J:130163 )
• agnathic mice exhibit small or absent eyes

skeleton
absent mandible ( J:130163 )
• in 3 of 126 mice age E14.5 to E18.5
short mandible ( J:130163 )
• in 2 of 126 mice age E14.5 to E18.5

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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Send questions and comments to User Support. 		last database update
12/10/2024
MGI 6.24 		The Jackson Laboratory