Slc22a14 Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Slc22a14
solute carrier family 22 (organic cation transporter), member 14
MGI:2685974

15 phenotypes from 1 allele in 1 genetic background

Allelic Composition Genetic Background	Annotated Term	Reference
Slc22a14^em1Fjw/Slc22a14^em1Fjw involves: C57BL/6N	abnormal ion homeostasis	J:322731
	abnormal pH regulation	J:322731
	abnormal sperm annulus morphology	J:277914
	abnormal sperm flagellum morphology	J:277914, J:322731
	asthenozoospermia	J:277914, J:322731
	decreased fertilization frequency	J:277914, J:322731
	decreased sperm progressive motility	J:277914
	hairpin sperm flagellum	J:277914
	impaired fertilization	J:277914
	impaired sperm capacitation	J:277914, J:322731
	impaired sperm migration in female genital tract	J:277914
	normal integument phenotype	J:277914
	kinked sperm flagellum	J:277914
	reduced male fertility	J:277914
	normal reproductive system phenotype	J:277914

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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