Cxxc1 Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Cxxc1
CXXC finger protein 1
MGI:1921572

21 phenotypes from 2 alleles in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Cxxc1^tm1Skk/Cxxc1^tm1Skk involves: 129S/SvEv * C57BL/6	abnormal ectoplacental cone morphology	J:72634
	absent embryonic epiblast	J:72634
	absent endoderm	J:72634
	embryonic lethality between implantation and somite formation, complete penetrance	J:72634
	empty decidua capsularis	J:72634
	failure to gastrulate	J:72634
Cxxc1^tm2.1Skk/Cxxc1^tm2.1Skk Tg(Stra8-icre)1Reb/0 involves: FVB/NJ	abnormal acrosome morphology	J:329283
	abnormal chromosomal synapsis	J:329283
	abnormal epigenetic regulation of gene expression	J:329283
	abnormal seminiferous tubule morphology	J:329283
	abnormal spermatogenesis	J:329283
	abnormal spermatogonia morphology	J:329283
	arrest of male meiosis	J:329283
	arrest of spermatogenesis	J:329283
	azoospermia	J:329283
	decreased male germ cell number	J:329283
	decreased testis weight	J:329283
	increased male germ cell apoptosis	J:329283
	male infertility	J:329283
	normal reproductive system phenotype	J:329283
	testis hypoplasia	J:329283

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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