Gsc Phenotype Annotations - Multigenic Genotypes

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Gsc
goosecoid homeobox
MGI:95841

39 phenotypes from multigenic genotypes

Allelic Composition Genetic Background	Annotated Term	Reference
Dkk1^tm1Lmgd/Dkk1⁺ Gsc^tm2Bhr/Gsc⁺ involves: 129S1/Sv * 129X1/SvJ * C57BL/6	decreased forebrain size	J:119933
Dkk1^tm1Lmgd/Dkk1⁺ Gsc^tm2Bhr/Gsc^tm2Bhr 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
Foxa2^tm1Jrt/Foxa2⁺ Gsc^tm1Bhr/Gsc^tm1Bhr 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
Foxa2^tm1Jrt/Foxa2^tm1Jrt Gsc^tm1Bhr/Gsc⁺ involves: 129/Sv * C57BL/6 * CD-1	abnormal embryo development	J:41809
	decreased embryo size	J:41809
Foxa2^tm1Jrt/Foxa2^tm1Jrt Gsc^tm1Bhr/Gsc^tm1Bhr involves: 129/Sv * C57BL/6 * CD-1	abnormal embryo development	J:41809
	decreased embryo size	J:41809
Gsc^tm1Bhr/Gsc^tm1Bhr Gsc2^tm1Bhr/Gsc2^tm1Bhr involves: 129S7/SvEvBrd * C57BL/6	normal embryo phenotype	J:50873
Gsc^tm1Pgr/Gsc^tm1Pgr Msx1^tm1Rilm/Msx1^tm1Rilm 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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