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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Axin1
axin 1
MGI:1096327
62 phenotypes from 7 alleles in 15 genetic backgrounds
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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
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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Send questions and comments to User Support. 		last database update
11/12/2024
MGI 6.24 		The Jackson Laboratory