43 phenotypes from 8 alleles in 10 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Fnip1em1(IMPC)Ccpcz/Fnip1em1(IMPC)Ccpcz C57BL/6NCrl-Fnip1em1(IMPC)Ccpcz/Ccpcz	abnormal spine curvature	J:211773
Fnip1Gt(RRM154)Byg/Fnip1Gt(RRM154)Byg involves: 129P2/OlaHsd * C57BL/6J	absent B cells	J:189078
	absent B-2 B cells	J:189078
	arrested B cell differentiation	J:189078
	decreased B cell number	J:189078
	decreased B-1 B cell number	J:189078
	decreased mature B cell number	J:189078
	decreased pre-B cell number	J:189078
	decreased transitional stage B cell number	J:189078
	increased B cell apoptosis	J:189078
	increased pro-B cell number	J:189078
	normal renal/urinary system phenotype	J:189078
	small spleen	J:189078
Fnip1LPAB.1/Fnip1LPAB.1 C57BL/6J-Fnip1LPAB.1	abnormal B cell physiology	J:187318
	abnormal skeletal muscle morphology	J:187318
	absent B cells	J:187318
	arrested B cell differentiation	J:187318
	cardiomyopathy	J:187318
	decreased B-1 B cell number	J:187318
	decreased IgE level	J:187318
	decreased IgG1 level	J:187318
	decreased IgG2a level	J:187318
	decreased IgG level	J:187318
	decreased IgM level	J:187318
	increased B cell apoptosis	J:187318
	increased liver glycogen level	J:187318
Fnip1m1Btlr/Fnip1m1Btlr C57BL/6J-Fnip1m1Btlr	abnormal bone marrow cell number	J:234285
	abnormal skeletal muscle morphology	J:234285
	abnormal splenocyte morphology	J:234285
	absent B cells	J:234285
	cardiac hypertrophy	J:234285
	normal cardiovascular system phenotype	J:234285
	decreased IgM level	J:234285
	decreased marginal zone B cell number	J:234285
	enhanced autophagy	J:234285
	enlarged heart	J:234285
	impaired hematopoiesis	J:234285
	increased cardiac muscle glycogen level	J:234285
	prolonged QRS complex duration	J:234285
	shortened PR interval	J:234285
Fnip1m2Btlr/Fnip1m2Btlr C57BL/6J-Fnip1m2Btlr	decreased B cell number	J:265134
	increased B-1 B cell number	J:265134
	increased CD4-positive, alpha-beta T cell number	J:265134
	increased single-positive T cell number	J:265134
	increased T cell number	J:265134
Fnip1M3Btlr/Fnip1M3Btlr C57BL/6J-Fnip1M3Btlr	abnormal B cell differentiation	J:272802
Fnip1tm1.1Baba/Fnip1tm1.1Baba Tg(Cdh16-cre)91Igr/0 involves: C57BL/6 * ICR	kidney cyst	J:220672
Fnip1tm1.1Baba/Fnip1tm1.1Baba Tg(Ckmm-cre)5Khn/0 involves: C57BL/6 * FVB	abnormal mitochondrial physiology	J:220672
	abnormal muscle morphology	J:220672
	abnormal muscle physiology	J:220672
	cardiac hypertrophy	J:220672
Fnip1tm1.2Baba/Fnip1tm1.2Baba involves: C57BL/6	premature death	J:220672
Fnip1tm1.2Baba/Fnip1tm1.2Baba involves: C57BL/6 * C57BL/6J * FVB/N * SJL	absent B cells	J:189078
	absent B-2 B cells	J:189078
	arrested B cell differentiation	J:189078
	decreased B cell number	J:189078
	decreased B-1 B cell number	J:189078
	decreased mature B cell number	J:189078
	decreased pre-B cell number	J:189078
	decreased transitional stage B cell number	J:189078
	increased B cell apoptosis	J:189078
	increased pro-B cell number	J:189078
	normal renal/urinary system phenotype	J:189078
	small spleen	J:189078