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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Gsc
goosecoid homeobox
MGI:95841
39 phenotypes from multigenic genotypes
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Allelic Composition
Genetic Background		 Annotated Term Reference
Dkk1tm1Lmgd/Dkk1+
Gsctm2Bhr/Gsc+
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 		decreased forebrain size J:119933
Dkk1tm1Lmgd/Dkk1+
Gsctm2Bhr/Gsctm2Bhr
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 		abnormal embryo development J:119933
abnormal eye development J:119933
decreased forebrain size J:119933
microcephaly J:119933
Foxa2tm1Jrt/Foxa2+
Gsctm1Bhr/Gsctm1Bhr
involves: 129 * C57BL/6 * CD-1 		abnormal anterior cardinal vein morphology J:41809
abnormal brain morphology J:41809
abnormal dorsal aorta morphology J:41809
abnormal dorsal-ventral axis patterning J:41809
abnormal embryo development J:41809
abnormal first pharyngeal arch artery morphology J:41809
abnormal first pharyngeal arch morphology J:41809
abnormal forebrain development J:41809
abnormal heart development J:41809
abnormal heart looping J:41809
abnormal neural tube morphology J:41809
abnormal notochord morphology J:41809
abnormal optic vesicle formation J:41809
abnormal pharyngeal arch morphology J:41809
abnormal pharynx morphology J:41809
abnormal second pharyngeal arch morphology J:41809
absent dorsal mesocardium J:41809
absent optic vesicle J:41809
decreased embryonic neuroepithelium thickness J:41809
decreased forebrain size J:41809
decreased hindbrain size J:41809
decreased somite size J:41809
decreased spinal cord size J:41809
embryonic growth arrest J:41809
embryonic growth retardation J:41809
embryonic lethality during organogenesis, complete penetrance J:41809
small first pharyngeal arch J:41809
small pharynx J:41809
small second pharyngeal arch J:41809
Foxa2tm1Jrt/Foxa2tm1Jrt
Gsctm1Bhr/Gsc+
involves: 129/Sv * C57BL/6 * CD-1 		abnormal embryo development J:41809
decreased embryo size J:41809
Foxa2tm1Jrt/Foxa2tm1Jrt
Gsctm1Bhr/Gsctm1Bhr
involves: 129/Sv * C57BL/6 * CD-1 		abnormal embryo development J:41809
decreased embryo size J:41809
Gsctm1Bhr/Gsctm1Bhr
Gsc2tm1Bhr/Gsc2tm1Bhr
involves: 129S7/SvEvBrd * C57BL/6 		normal embryo phenotype J:50873
Gsctm1Pgr/Gsctm1Pgr
Msx1tm1Rilm/Msx1tm1Rilm
involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ 		abnormal Meckel's cartilage morphology J:59750
abnormal tympanic cavity morphology J:59750
absent external auditory canal J:59750
absent malleus processus brevis J:59750
cleft palate J:59750
decreased tympanic ring size J:59750
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
04/23/2024
MGI 6.23 		The Jackson Laboratory