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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Tgdsem1(IMPC)Mbp
endonuclease-mediated mutation 1, Mouse Biology Program, UC Davis
MGI:6430646
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Tgdsem1(IMPC)Mbp/Tgdsem1(IMPC)Mbp C57BL/6NCrl-Tgdsem1(IMPC)Mbp/Mmucd MGI:6696936
ht2
Tgdsem1(IMPC)Mbp/Tgds+ C57BL/6NCrl-Tgdsem1(IMPC)Mbp/Mmucd MGI:7267107


Genotype
MGI:6696936
hm1
Allelic
Composition
Tgdsem1(IMPC)Mbp/Tgdsem1(IMPC)Mbp
Genetic
Background
C57BL/6NCrl-Tgdsem1(IMPC)Mbp/Mmucd
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tgdsem1(IMPC)Mbp mutation (1 available); any Tgds mutation (20 available)
Data Sources
phenotype observed in females
phenotype observed in males
N normal phenotype

Tgdsem1(IMPC)Mbp/Tgdsem1(IMPC)Mbp embryos have abnormal head shape, abnormal hearts accompanied by cardiac or pericardial edema, abnormal yolk sac morphology, and branchial arch defects and incomplete turning at E9.5. By E10.5, embryos are grossly abnormal.

cardiovascular system
IMPC - UCD (J:211773)
MGI
• by E9.5, many homozygous embryos show abnormal heart morphology, some with cardiac or pericardial edema (J:374598)
• by E10.5, all embryos recovered intact show grossly abnormal hearts with severe pericardial edema (J:374598)
• at E9.5, some homozygous embryos show inappropriate heart looping (J:374598)
IMPC - UCD (J:211773)
• at E9.5, some homozygous embryos exhibit an enlarged heart
• by E9.5, some homozygous embryos exhibit pericardial edema
• by E10.5, all embryos recovered intact show severe pericardial edema

craniofacial
• at E9.5, a minority of homozygous embryos show branchial arch defects
• at E9.5, most homozygous embryos exhibit an abnormal head shape, particularly evident in the forebrain
• by E10.5, all embryos recovered intact show an abnormal head shape

embryo
• at E9.5, a minority of homozygous embryos show incomplete turning
• by E10.5, all embryos recovered intact are developmentally delayed relative to control littermates
• however, all three germ layers are present at E8.5 and properly patterned at E9.5
• all embryonic phenotypes are more pronounced in older E9.5 homozygous embryos
• by E10.5, all homozygous embryos are grossly abnormal and either dead or dying
• however, at E8.5, nearly all are indistinguishable from control littermates
• at E9.5, a minority of homozygous embryos show branchial arch defects
• at E10.5, placentas exhibit multiple labyrinth zone defects
• at E10.5, the Tfeb+ labyrinth trophoblast layer is reduced
• by E9.5, when dissected intact, most homozygous embryos show abnormal yolk sac morphology
• at E10.5, chorioallantoic branching is nearly absent, as Gcm1 expression is sparse and remains at the chorioallantoic interface
• however, placentas appear properly developed at E9.5
• at E10.5, placentas exhibit an abnormal chorioallantoic interface with a reduction in allantoic mesoderm

growth/size/body
• at E9.5, some homozygous embryos exhibit an enlarged heart
• at E9.5, most homozygous embryos exhibit an abnormal head shape, particularly evident in the forebrain
• by E10.5, all embryos recovered intact show an abnormal head shape
• by E10.5, all embryos recovered intact are developmentally delayed relative to control littermates
• however, all three germ layers are present at E8.5 and properly patterned at E9.5

homeostasis/metabolism
• by E9.5, some homozygous embryos exhibit pericardial edema
• by E10.5, all embryos recovered intact show severe pericardial edema
• by E9.5, some homozygous embryos exhibit cardiac edema

mortality/aging
• homozygous embryos are present in Mendelian ratios at E8.5 and E9.5; by E10.5, all homozygous embryos are either dead or dying

nervous system
• at E9.5, most homozygous embryos exhibit an abnormal forebrain shape

vision/eye




Genotype
MGI:7267107
ht2
Allelic
Composition
Tgdsem1(IMPC)Mbp/Tgds+
Genetic
Background
C57BL/6NCrl-Tgdsem1(IMPC)Mbp/Mmucd
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tgdsem1(IMPC)Mbp mutation (1 available); any Tgds mutation (20 available)
Data Sources
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological

cardiovascular system

embryo

endocrine/exocrine glands
IMPC - UCD

homeostasis/metabolism

renal/urinary system
IMPC - UCD

reproductive system
IMPC - UCD

vision/eye
IMPC - UCD





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last database update
01/06/2026
MGI 6.24
The Jackson Laboratory