Phenotypes associated with this allele

• Allele Symbol: Esrp2⁺
• Allele Name: wild type
• Allele ID: MGI:3588733
• Summary: 1 genotype

Jump to	Allelic Composition	Genetic Background	Genotype ID
cx1	Esrp1^tm1.2Rpc/Esrp1^tm1.2Rpc Esrp2^tm1(KOMP)Vlcg/Esrp2^+	involves: 129S4/SvJae * C57BL/6 * C57BL/6J * C57BL/6NTac	MGI:5707286

Genotype
MGI:5707286

cx1

• Allelic Composition: Esrp1^tm1.2Rpc/Esrp1^tm1.2Rpc; Esrp2^{tm1(KOMP)Vlcg}/Esrp2⁺
• Genetic Background: involves: 129S4/SvJae * C57BL/6 * C57BL/6J * C57BL/6NTac
• Cell Lines: 13762A-G3

• ♀: phenotype observed in females
• ♂: phenotype observed in males
• N: normal phenotype

craniofacial

abnormal mandible morphology ( J:226997 )

• mandibular dysplasia

mandible hypoplasia ( J:226997 )

bilateral cleft upper lip ( J:226997 )

• bilateral cleft lip at E18.5

cleft palate ( J:226997 )

cleft primary palate ( J:226997 )

• clefting of the primary palate is seen at E18.5

cleft hard palate ( J:226997 )

• clefting of the secondary hard palate is seen at E18.5

cleft soft palate ( J:226997 )

• clefting of the secondary soft palate is seen at E18.5

digestive/alimentary system

cleft palate ( J:226997 )

cleft primary palate ( J:226997 )

• clefting of the primary palate is seen at E18.5

cleft hard palate ( J:226997 )

• clefting of the secondary hard palate is seen at E18.5

cleft soft palate ( J:226997 )

• clefting of the secondary soft palate is seen at E18.5

embryo

short rostral-caudal axis ( J:226997 )

• rostral shortening

growth/size/body

abnormal mandible morphology ( J:226997 )

• mandibular dysplasia

mandible hypoplasia ( J:226997 )

bilateral cleft upper lip ( J:226997 )

• bilateral cleft lip at E18.5

cleft palate ( J:226997 )

cleft primary palate ( J:226997 )

• clefting of the primary palate is seen at E18.5

cleft hard palate ( J:226997 )

• clefting of the secondary hard palate is seen at E18.5

cleft soft palate ( J:226997 )

• clefting of the secondary soft palate is seen at E18.5

abnormal fetal growth/weight/body size ( J:226997 )

• slight length reduction at E18.5

decreased fetal weight ( J:226997 )

• slight weight reduction at E18.5

limbs/digits/tail

syndactyly ( J:226997 )

• embryos often show forepaw syndactyly

abnormal forelimb morphology ( J:226997 )

• embryos often show malformed forelimbs

absent humerus ( J:226997 )

absent radius ( J:226997 )

skeleton

abnormal mandible morphology ( J:226997 )

• mandibular dysplasia

mandible hypoplasia ( J:226997 )

absent humerus ( J:226997 )

absent radius ( J:226997 )