73 phenotypes from multigenic genotypes

Allelic Composition Genetic Background	Annotated Term	Reference
Btnl1tm1(KOMP)Mbp/Btnl1tm1(KOMP)Mbp Foxn1nu/Foxn1nu involves: albino stock * C57BL/6N	decreased gamma-delta intraepithelial T cell number	J:236526
Dh/Dh+ Foxn1nu/Foxn1nu involves: N:NIH(S)	abnormal Peyer's patch morphology	J:6062
	absent spleen	J:6062
	athymia	J:6062
	decreased leukocyte cell number	J:6062
	increased erythroid progenitor cell number	J:6062
	increased IgA level	J:6062
	thrombocytosis	J:6062
Dicer1tm1Tara/Dicer1tm1Tara Foxn1tm3(cre)Nrm/Foxn1+ involves: 129P2/OlaHsd * C57BL/6NHsd	abnormal positive T cell selection	J:180783
	abnormal thymus cortex morphology	J:180783
	abnormal thymus epithelium morphology	J:180783
	abnormal thymus involution	J:180783
	abnormal thymus medulla morphology	J:180783
	abnormal thymus morphology	J:180783
	abnormal thymus physiology	J:180783
	decreased CD4-positive, alpha-beta T cell number	J:180783
	decreased CD8-positive, alpha-beta T cell number	J:180783
	increased susceptibility to induced arthritis	J:180783
Dll4tm1Frad/Dll4tm1Frad Foxn1tm3(cre)Nrm/Foxn1+ B6.Cg-Dll4tm1Frad Foxn1tm3(cre)Nrm	abnormal T cell differentiation	J:143472
	abnormal thymus cell ratio	J:143472
	decreased CD4-positive, alpha-beta T cell number	J:143472
	decreased CD8-positive, alpha-beta T cell number	J:143472
	decreased double-positive T cell number	J:143472
	decreased thymocyte number	J:143472
	increased immature B cell number	J:143472
Dmdmdx/Y Foxn1nu/Foxn1nu involves: C57BL/10ScSn	abnormal muscle morphology	J:95776
	decreased skeletal muscle fiber size	J:95776
	increased skeletal muscle fiber size	J:95776
Foxn1nu/Foxn1nu Fv4r/Fv4r involves: BALB/c	decreased susceptibility to Retroviridae infection	J:5684, J:5714
Foxn1nu/Foxn1nu Gpc1tm1.1Alan/Gpc1tm1.1Alan involves: CD-1	abnormal response/metabolism to endogenous compounds	J:130809
	decreased metastatic potential	J:130809
Foxn1nu/Foxn1nu Ivltm1Dji/Ivltm1Dji involves: 129S4/SvJae * BALB/c * C57BL/6	no abnormal phenotype detected	J:65192
Foxn1nu/Foxn1nu Map3k14aly/Map3k14aly involves: BALB/cAJcl * C57BL/6J	absent B cells	J:96579
	absent lymph nodes	J:96579
	absent Peyer's patches	J:96579
	athymia	J:96579
	decreased gamma-delta intraepithelial T cell number	J:96579
	decreased T cell number	J:96579
Foxn1nu/Foxn1nu Msx2tm1Rilm/Msx2tm1Rilm involves: 129S4/SvJae * BALB/c * CD-1	abnormal nail bed morphology	J:173664
	abnormal nail matrix morphology	J:173664
	abnormal nail morphology	J:173664
	abnormal nail plate morphology	J:173664
	deformed nails	J:173664
	short nails	J:173664
Foxn1nu/Foxn1nu Srcr/Srcr+ involves: BALB/c * C57BL/6	decreased tumor incidence	J:83618
Foxn1nu/Foxn1nu Tg(Foxn1)E1Hon/0 involves: CD-1	athymia	J:33866
	hairless	J:33866
Foxn1nu/Foxn1nu Tg(Foxn1)G2Hon/0 involves: CD-1	hairless	J:33866
	infertility	J:33866
Foxn1nu/Foxn1nu Tgfb1tm1Doe/Tgfb1tm1Doe involves: 129S2/SvPas * BALB/c * CF-1	abnormal T cell physiology	J:99033
	decreased inflammatory response	J:99033
	premature death	J:99033
Foxn1tm3(cre)Nrm/Foxn1+ Gt(ROSA)26Sortm1(Tbx1)Rche/Gt(ROSA)26Sor+ involves: C57BL/6 * C57BL/6NHsd	abnormal third pharyngeal pouch morphology	J:214094
	abnormal thymus development	J:214094
	abnormal thymus epithelium morphology	J:214094
	decreased thymocyte number	J:214094
	thymus hypoplasia	J:214094
Foxn1tm3(cre)Nrm/Foxn1+ Mir205hgtm1Oers/Mir205hgtm1Oers B6(Cg)-Mir205hgtm1Oers Foxn1tm3(cre)Nrm	decreased thymocyte number	J:278363
	decreased thymus weight	J:278363
	thymus hypoplasia	J:278363
Foxp3tm1Ayr/Foxp3tm1Ayr Foxn1tm3(cre)Nrm/Foxn1+ involves: 129S1/Sv * 129X1/SvJ * C57BL/6	normal immune system phenotype	J:125405
Gt(ROSA)26Sortm1(CAG-Foxn1/ERT2,-GFP)Cbln/Gt(ROSA)26Sor+ Foxn1tm3(cre)Nrm/Foxn1+ involves: 129P2/OlaHsd * C57BL/6	abnormal thymus involution	J:208852
	normal endocrine/exocrine gland phenotype	J:208852
	increased T cell number	J:208852
Tg(Foxn1)1Jlb/0 involves: C57BL/6 * DBA	absent eyelids	J:56641
	decreased body size	J:56641
	flaky skin	J:56641
	impaired skin barrier function	J:56641
	neonatal lethality, complete penetrance	J:56641
	shiny skin	J:56641
	tight skin	J:56641
Tg(Foxn1)6Jlb/0 involves: C57BL/6 * DBA	alopecia	J:56641
	curly vibrissae	J:56641
	decreased birth body size	J:56641
	delayed hair appearance	J:56641
	hydronephrosis	J:56641
	kinked vibrissae	J:56641
	loss of vibrissae	J:56641
	premature death	J:56641
	scaly muzzle	J:56641
	short hair	J:56641
	sparse hair	J:56641
	underdeveloped hair follicles	J:56641
	ureter urothelium hyperplasia	J:56641
	waved hair	J:56641