Sohlh2 Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Sohlh2
spermatogenesis and oogenesis specific basic helix-loop-helix 2
MGI:1921684

17 phenotypes from 3 alleles in 3 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Sohlh2^tm1Fkh/Sohlh2^tm1Fkh involves: 129S6/SvEvTac * C57BL/6	abnormal spermatocyte morphology	J:220953
	abnormal spermatogonia morphology	J:220953
	arrest of spermatogenesis	J:220953
	decreased male germ cell number	J:220953
	decreased testis weight	J:220953
	male infertility	J:220953
	small testis	J:220953
	testicular atrophy	J:220953
Sohlh2^tm1Miya/Sohlh2^tm1Miya involves: 129P2/OlaHsd * C57BL/6	abnormal oogenesis	J:143535
	abnormal spermatocyte morphology	J:143535
	abnormal spermatogonia morphology	J:143535
	absent ovarian follicles	J:143535
	female infertility	J:143535
	impaired ovarian folliculogenesis	J:143535
	male infertility	J:143535
	ovary atrophy	J:143535
	testicular atrophy	J:143535
Sohlh2^tm1Rajk/Sohlh2^tm1Rajk involves: 129S7/SvEvBrd * C57BL/6	abnormal ovarian follicle number	J:145802
	decreased oocyte number	J:145802
	decreased primary ovarian follicle number	J:145802
	female infertility	J:145802
	impaired granulosa cell differentiation	J:145802
	ovary atrophy	J:145802

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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