Fmn1 Phenotype Annotations - Multigenic Genotypes

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Fmn1
formin 1
MGI:101815

39 phenotypes from multigenic genotypes

Allelic Composition Genetic Background	Annotated Term	Reference
a^{jIs(17;In2)1Gso}/a^{jIs(17;In2)1Gso} Fmn1^{ld-Is(17;In2)1Gso}/Fmn1^{ld-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
Alx4^lst/Alx4⁺ Fmn1^ld-TgHD/Fmn1⁺ involves: BALB/c * C57BL/6 * CD-1 * FVB/N	normal limbs/digits/tail phenotype	J:17401
Fmn1^em1Zllr/Fmn1^em1Zllr involves: Swiss albino	syndactyly	J:312378
Fmn1^em1Zllr/Fmn1^em1Zllr Rr287^em1Zllr/Rr287^em1Zllr involves: Swiss albino	forelimb oligodactyly	J:312378
Fmn1^em1Zllr/Fmn1^em2Zllr involves: Swiss albino	forelimb oligodactyly	J:312378
Fmn1^em1Zllr/Fmn1^em2Zllr involves: Swiss albino	syndactyly	J:312378
Fmn1^em2Zllr/Fmn1^em2Zllr involves: Swiss albino	limbs/digits/tail phenotype	J:312378
Fmn1^em3Zllr/Fmn1^em3Zllr involves: Swiss albino	limbs/digits/tail phenotype	J:312378
Fmn1^em3Zllr/Fmn1^em3Zllr Rr26^em1Zllr/Rr26^em1Zllr involves: Swiss albino	limbs/digits/tail phenotype	J:312378
Fmn1^em3Zllr/Fmn1^em3Zllr Rr284^em1Zllr/Rr284^em1Zllr involves: Swiss albino	limbs/digits/tail phenotype	J:312378
Fmn1^em3Zllr/Fmn1^em3Zllr Rr287^em1Zllr/Rr287^em1Zllr involves: Swiss albino	limbs/digits/tail phenotype	J:312378
Fmn1^ld-Lsk/Fmn1^ld-Lsk C.Cg-Fmn1^ld-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
Fmn1^ld-TgBri137/Fmn1^tm1Led involves: 129S6/SvEvTac * Black Swiss * C57BL/6 * SJL	absent kidney	J:50647
	single kidney	J:50647
Fmn1^ld-TgHD/Fmn1^ld-TgHD involves: BALB/c * C57BL/6 * CD-1 * FVB/N	abnormal kidney morphology	J:17401
	absent kidney	J:17401
	single kidney	J:17401
Fmn1^ld-TgHD/Fmn1^ld-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
Fmn1^tm1Awb/Fmn1^{ld-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
Fmn1^tm1Awb/Fmn1^ld-TgBri137 involves: 129S4/SvJae * C57BL/6 * NIH Black Swiss * SJL	normal limbs/digits/tail phenotype	J:43337
	single kidney	J:43337
Fmn1^tm2Made/Fmn1⁺ Grem1^tm1Azun/Grem1⁺ involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ * C57BL/6J	abnormal limb development	J:149484

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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