62 phenotypes from 7 alleles in 15 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Axin1Fu-kb/Axin1+ Not Specified	kinked tail	J:13701
Axin1Fu-kb/Axin1Fu-kb Not Specified	abnormal developmental patterning	J:13850
	abnormal ectoderm development	J:13850
	embryonic lethality, complete penetrance	J:13850
	impaired spacing of implantation sites	J:13850
	small amniotic cavity	J:13850
	twin decidual capsule	J:13850
Axin1Fu-ki/Axin1+ mixed	abnormal caudal vertebrae morphology	J:13056
	abnormal lumbar vertebrae morphology	J:13056
	abnormal sacral vertebrae morphology	J:13056
	abnormal thoracic vertebrae morphology	J:13056
	abnormal vertebrae morphology	J:13056
	bifurcated tail	J:13056
	caudal vertebral fusion	J:13056
	decreased caudal vertebrae number	J:13056
	kinked tail	J:13056
	lumbar vertebral fusion	J:13056
	rib fusion	J:13056
	sacral vertebral fusion	J:13056
	short tail	J:13056
	thoracic vertebral fusion	J:13056
Axin1Fu-ki/Axin1Fu-ki involves: Bagg albino * CF * fancier's mice	abnormal allantois morphology	J:13017
	abnormal embryonic tissue morphology	J:13017
	abnormal extraembryonic tissue morphology	J:13017
	disorganized embryonic tissue	J:13017
	embryonic growth retardation	J:13017
	embryonic lethality during organogenesis, complete penetrance	J:13017
	rostral-caudal axis duplication	J:13017
	small tail bud	J:13017
	split notochord	J:13017
Axin1Fu-ki/Axin1Fu-ki involves: BTBR	abnormal cephalic neural fold morphology	J:28303
	kinked neural tube	J:28303
Axin1Fu-ki/Axin1Fu-ki mixed	prenatal lethality	J:13056
Axin1Fu-ki/Axin1Fu-Tg1 involves: BTBR * C57BL/6J * CBA/J	abnormal allantois morphology	J:28303
	abnormal cephalic neural fold morphology	J:28303
	embryonic growth retardation	J:28303
	enlarged pericardium	J:28303
	flat head	J:28303
Axin1Fu-Tg1/Axin1Fu-Tg1 involves: C57BL/6J * CBA/J	abnormal allantois morphology	J:28303
	abnormal amniotic cavity morphology	J:28303
	abnormal axial mesoderm morphology	J:41619
	abnormal embryonic tissue morphology	J:28303
	absent forebrain	J:28303
	cardia bifida	J:28303, J:147293
	decreased embryo size	J:147293
	embryonic growth retardation	J:28303, J:147293
	embryonic lethality during organogenesis, complete penetrance	J:28303
	enlarged pericardium	J:28303, J:147293
	forebrain hypoplasia	J:28303
	incomplete rostral neuropore closure	J:28303, J:147293
	kinked neural tube	J:28303
	rostral-caudal axis duplication	J:28303
	shortened head	J:147293
Axin1Fu/Axin1+ 129P4.Cg-Axin1Fu/J	genetic imprinting	J:82396
	maternal imprinting	J:82396
	paternal imprinting	J:82396
Axin1Fu/Axin1+ involves: 129/Rr * C3H/He * C57BL/6J	genetic imprinting	J:6577
	paternal imprinting	J:6577
Axin1Fu/Axin1+ involves: 129/Rr * C3H/He * C57BL/6J * wild	genetic imprinting	J:6577
Axin1Fu/Axin1+ involves: 129P4/RrRk * TF/Le	reversion by viral sequence excision	J:68896
Axin1Fu/Axin1+ involves: C57BL/6J * CBA/Lac	paternal imprinting	J:133043
Axin1Fu/Axin1+ involves: M. m. bactrianus	no abnormal phenotype detected	J:12953
Axin1Fu/Axin1+ Not Specified	abnormal axial skeleton morphology	J:12953
	abnormal caudal vertebrae morphology	J:12953
	abnormal craniofacial bone morphology	J:12112
	abnormal hindlimb morphology	J:12953
	abnormal kidney development	J:12112
	abnormal tail length	J:12953
	abnormal vertebrae morphology	J:12953
	absent kidney	J:12112
	absent ribs	J:12953
	bifurcated tail	J:12953
	circling	J:242
	deafness	J:242
	decreased caudal vertebrae number	J:12953
	maternal effect	J:12953
	rectal atresia	J:12112
	rib fusion	J:12953
	urethra atresia	J:12112
Axin1Fu/Axin1Fu Not Specified	abnormal axial skeleton morphology	J:12953
	abnormal caudal vertebrae morphology	J:12953
	abnormal craniofacial bone morphology	J:242
	abnormal hindlimb morphology	J:12953
	abnormal kidney development	J:12112
	abnormal tail morphology	J:67881
	abnormal vertebrae morphology	J:12953
	absent kidney	J:12953
	absent ribs	J:12953
	absent ureter	J:12953
	bifurcated tail	J:12953
	circling	J:242
	deafness	J:242
	decreased caudal vertebrae number	J:12953
	maternal effect	J:12953
	rectal atresia	J:12112
	rib fusion	J:12953
	short tail	J:12953
	urethra atresia	J:12112
Axin1tm1.1Dic/Axin1tm1.1Dic involves: 129S4/SvJaeSor * C57BL/6	no abnormal phenotype detected	J:169694
Axin1tm1.2Dic/Axin1tm1.2Dic involves: 129S4/SvJaeSor * BALB/cJ * C57BL/6	abnormal embryonic tissue morphology	J:169694
	decreased embryo size	J:169694
	embryonic lethality	J:169694
Axin1tm2Cos/Axin1tm2Cos involves: 129S6/SvEvTac * FVB/N	no abnormal phenotype detected	J:98893