40 phenotypes from 2 alleles in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Pfdn5nmf5a/Pfdn5nmf5a C57BL/6-Pfdn5nmf5a	abnormal brain ependyma motile cilium morphology	J:167349
	abnormal choroid plexus morphology	J:167349
	abnormal eye electrophysiology	J:167349
	abnormal nervous system physiology	J:167349
	abnormal photoreceptor outer segment morphology	J:167349
	abnormal retina apoptosis	J:167349
	abnormal retina morphology	J:167349
	abnormal retina outer limiting membrane morphology	J:167349
	abnormal retina photoreceptor morphology	J:167349
	ataxia	J:167349
	decreased brain ependyma motile cilium number	J:167349
	decreased brain weight	J:167349
	decreased Purkinje cell number	J:167349
	dilated third ventricle	J:167349
	disorganized photoreceptor outer segment	J:167349
	early reproductive senescence	J:167349
	hydrocephaly	J:167349
	male infertility	J:167349
	necrospermia	J:167349
	oligozoospermia	J:167349
	pregnancy-related premature death	J:167349
	premature death	J:167349
	normal reproductive system phenotype	J:167349
	retina photoreceptor degeneration	J:167349
	short photoreceptor inner segment	J:167349
	short photoreceptor outer segment	J:167349
	small cerebellum	J:167349
	small testis	J:167349
	thin retina inner nuclear layer	J:167349
	thin retina outer nuclear layer	J:167349
Pfdn5tm1b(EUCOMM)Wtsi/Pfdn5+ C57BL/6N-Pfdn5tm1b(EUCOMM)Wtsi/Bay	decreased lean body mass	J:211773
	increased total body fat amount	J:211773
Pfdn5tm1b(EUCOMM)Wtsi/Pfdn5tm1b(EUCOMM)Wtsi C57BL/6N-Pfdn5tm1b(EUCOMM)Wtsi/Bay	abnormal craniofacial morphology	J:211773
	abnormal embryo size	J:211773
	abnormal skin coloration	J:211773
	abnormal tail morphology	J:211773
	edema	J:211773
	embryonic growth retardation	J:211773
	prenatal lethality	J:211773
	preweaning lethality, complete penetrance	J:211773