49 phenotypes from multigenic genotypes

Allelic Composition Genetic Background	Annotated Term	Reference
a/a Hps6ru-5J/Hps6ru-5J Lystbg/Lystbg involves: C3H/Rl * C57BL/6J	abnormal coat/hair pigmentation	J:26546
	abnormal eye pigmentation	J:26546
	decreased eye pigmentation	J:26546
	diluted coat color	J:26546
a/a Hps6ru/Hps6ru Lystbg/Lystbg involves: C3H/Rl * C57BL/6J	abnormal melanogenesis	J:5346
	abnormal melanosome morphology	J:5346
	abnormal retina melanin granule morphology	J:5346
a/a Lystbg/Lystbg involves: C3H/Rl * C57BL/6J	abnormal choroid melanin granule morphology	J:5346
	abnormal retina melanin granule morphology	J:5346
a/a Lystbg/Lystbg Oca2p-J/Oca2p-J involves: C3H/HeJ * C3H/Rl * C57BL/6J	abnormal choroid melanin granule morphology	J:5346
	abnormal melanosome morphology	J:5346
a/a Lystbg/Lystbg Tyrc/Tyrc involves: C3H/Rl * C57BL/6J	abnormal choroid melanin granule morphology	J:5346
	abnormal melanogenesis	J:5346
	abnormal melanosome morphology	J:5346
	abnormal retina melanin granule morphology	J:5346
a/a Lystbg/Lystbg Tyrp1b/Tyrp1b involves: C3H/Rl * C57BL/6J	abnormal choroid melanin granule morphology	J:5346
	abnormal retina melanin granule morphology	J:5346
A/? Lystbg/Lystbg Tyrp1+/? Not Specified	abnormal eye pigmentation	J:29744
	decreased ear pigmentation	J:29744
	decreased tail pigmentation	J:29744
	diluted coat color	J:29744
	irregular coat pigmentation	J:29744
A/? Lystbg/Lystbg Tyrp1b/Tyrp1b Not Specified	decreased eye pigmentation	J:29744
	diluted coat color	J:29744
Ednrbs/Ednrbs Lystbg-slt/Lystbg-slt involves: C57BL/10Ch * Y257/Ch	abnormal eye pigmentation	J:25388
Foxq1sa/Foxq1sa Lystbg/Lystbg involves: 101/Rl * C3H/Rl * C57BL10/Rl	enlarged spleen	J:5311
	interstitial pneumonia	J:5311
	lung inflammation	J:5311
	weight loss	J:5311
Foxq1sa/Foxq1sa Lystbg/Lystbg involves: 101/Rl * C3H/Rl * C57BL/6J * C57BL10/Rl	enlarged lymph nodes	J:5311
	increased lymphoma incidence	J:5311
	increased susceptibility to infection	J:5311
	interstitial pneumonia	J:5311, J:15166
	premature death	J:15166
Hps6ru/Hps6ru Lystbg-slt/Lystbg-slt involves: YZ57/Ch	decreased eye pigmentation	J:25388
	diluted coat color	J:25388
Lystbg-J/Lystbg-J Prkdcscid/Prkdcscid B6.Cg-Lystbg-J Prkdcscid/Sz	abnormal complement pathway	J:34814
	abnormal granulocyte morphology	J:34814
	abnormal level of surface class II molecules	J:34814
	abnormal lymph node morphology	J:34814
	abnormal neutrophil morphology	J:34814
	abnormal Peyer's patch morphology	J:34814
	abnormal spleen white pulp morphology	J:34814
	abnormal thymus morphology	J:34814
	decreased B cell number	J:34814
	decreased CD4-positive, alpha-beta T cell number	J:34814
	decreased CD8-positive, alpha-beta T cell number	J:34814
	decreased immunoglobulin level	J:34814
	decreased lymphocyte cell number	J:34814
	decreased pre-B cell number	J:34814
	decreased T cell number	J:34814
	impaired natural killer cell mediated cytotoxicity	J:34814
	increased eosinophil cell number	J:34814
	increased granulocyte number	J:34814
	increased macrophage cell number	J:34814
	increased monocyte cell number	J:34814
	increased neutrophil cell number	J:34814
	increased NK cell number	J:34814
	small Peyer's patches	J:34814
	small thymus	J:34814
	spleen hypoplasia	J:34814
	thymus cyst	J:34814
Lystbg-slt/Lystbg-slt Myo5ad/Myo5ad involves: CT/Ch * YZ57/Ch	diluted coat color	J:25388
	normal vision/eye phenotype	J:25388
Lystbg-slt/Lystbg-slt Myo5ad/Myo5ad Oca2p/Oca2p Tyrp1b/Tyrp1b involves: CT/Ch * YZ57/Ch	abnormal hair cycle	J:83269
	delayed hair regrowth	J:83269
	diluted coat color	J:83269
	premature hair loss	J:83269
Lystbg-slt/Lystbg-slt Oca2p/Oca2p involves: CT/Ch * YZ57/Ch	abnormal eye pigmentation	J:25388
	diluted coat color	J:25388
Lystbg/Lystbg Prkdcscid/Prkdcscid Not Specified	increased susceptibility to infection	J:4752