39 phenotypes from multigenic genotypes

Allelic Composition Genetic Background	Annotated Term	Reference
ajIs(17;In2)1Gso/ajIs(17;In2)1Gso Fmn1ld-Is(17;In2)1Gso/Fmn1ld-Is(17;In2)1Gso involves: 101/Rl * C3H/Rl * C57BL/E * SEC/Rl	abnormal autopod morphology	J:10399
	abnormal autopod rotation	J:10399
	abnormal carpal bone morphology	J:10399
	abnormal forelimb morphology	J:10399
	abnormal hindlimb morphology	J:10399
	abnormal patella morphology	J:10399
	abnormal radius morphology	J:10399
	abnormal tarsal bone morphology	J:10399
	abnormal ulna morphology	J:10399
	absent fibula	J:10399
	brachydactyly	J:10399
	darkened coat color	J:10399
	dilated ureter	J:10399
	fused carpal bones	J:10399
	fused tarsal bones	J:10399
	hydronephrosis	J:10399
	hydroureter	J:10399
	oligodactyly	J:10399
	radius hypoplasia	J:10399
	renal hypoplasia	J:10399
	single kidney	J:10399
	syndactyly	J:10399
	synostosis	J:10399
Alx4lst/Alx4+ Fmn1ld-TgHD/Fmn1+ involves: BALB/c * C57BL/6 * CD-1 * FVB/N	normal limbs/digits/tail phenotype	J:17401
Fmn1em1Zllr/Fmn1em1Zllr involves: Swiss albino	syndactyly	J:312378
Fmn1em1Zllr/Fmn1em1Zllr Rr287em1Zllr/Rr287em1Zllr involves: Swiss albino	forelimb oligodactyly	J:312378
Fmn1em1Zllr/Fmn1em2Zllr involves: Swiss albino	forelimb oligodactyly	J:312378
	syndactyly	J:312378
Fmn1em2Zllr/Fmn1em2Zllr involves: Swiss albino	limbs/digits/tail phenotype	J:312378
Fmn1em3Zllr/Fmn1em3Zllr involves: Swiss albino	limbs/digits/tail phenotype	J:312378
Fmn1em3Zllr/Fmn1em3Zllr Rr26em1Zllr/Rr26em1Zllr involves: Swiss albino	limbs/digits/tail phenotype	J:312378
Fmn1em3Zllr/Fmn1em3Zllr Rr284em1Zllr/Rr284em1Zllr involves: Swiss albino	limbs/digits/tail phenotype	J:312378
Fmn1em3Zllr/Fmn1em3Zllr Rr287em1Zllr/Rr287em1Zllr involves: Swiss albino	limbs/digits/tail phenotype	J:312378
Fmn1ld-Lsk/Fmn1ld-Lsk C.Cg-Fmn1ld-Lsk	abnormal autopod morphology	J:123068
	abnormal autopod rotation	J:123068
	abnormal calcaneum morphology	J:123068
	abnormal limb morphology	J:123068
	abnormal radius morphology	J:123068
	abnormal ulna morphology	J:123068
	absent fibula	J:123068
	short tibia	J:123068
Fmn1ld-TgBri137/Fmn1tm1Led involves: 129S6/SvEvTac * Black Swiss * C57BL/6 * SJL	absent kidney	J:50647
	single kidney	J:50647
Fmn1ld-TgHD/Fmn1ld-TgHD involves: BALB/c * C57BL/6 * CD-1 * FVB/N	abnormal kidney morphology	J:17401
	absent kidney	J:17401
	single kidney	J:17401
Fmn1ld-TgHD/Fmn1ld-TgHD involves: C57BL/6 * CD-1	abnormal fibula morphology	J:8077
	abnormal forelimb morphology	J:8077
	abnormal hindlimb morphology	J:8077
	abnormal tibia morphology	J:8077
	fused carpal bones	J:8077
	fused metacarpal bones	J:8077
	fused metatarsal bones	J:8077
	fused phalanges	J:8077
	fused radius and ulna	J:8077
	fused tarsal bones	J:8077
	oligodactyly	J:8077
	normal skeleton phenotype	J:8077
	syndactyly	J:8077
Fmn1tm1Awb/Fmn1ld-Is(17;In2)1Gso involves: 101/Rl * 129S4/SvJae * C3H/Rl * NIH Black Swiss	normal limbs/digits/tail phenotype	J:43337
	polycystic kidney	J:43337
Fmn1tm1Awb/Fmn1ld-TgBri137 involves: 129S4/SvJae * C57BL/6 * NIH Black Swiss * SJL	normal limbs/digits/tail phenotype	J:43337
	single kidney	J:43337
Fmn1tm2Made/Fmn1+ Grem1tm1Azun/Grem1+ involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ * C57BL/6J	abnormal limb development	J:149484