Phenotypes associated with this allele

• Allele Symbol: Pccb^{tm1.1(KOMP)Vlcg}
• Allele Name: targeted mutation 1.1, Velocigene
• Allele ID: MGI:5708203
• Summary: 2 genotypes

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	Pccb^tm1.1(KOMP)Vlcg/Pccb^tm1.1(KOMP)Vlcg	C57BL/6N-Pccb^tm1.1(KOMP)Vlcg/Ucd	MGI:5767752
ht2	Pccb^tm1.1(KOMP)Vlcg/Pccb^+	C57BL/6N-Pccb^tm1.1(KOMP)Vlcg/Ucd	MGI:6461515

Genotype
MGI:5767752

hm1

• Allelic Composition: Pccb^{tm1.1(KOMP)Vlcg}/Pccb^{tm1.1(KOMP)Vlcg}
• Genetic Background: C57BL/6N-Pccb^{tm1.1(KOMP)Vlcg}/Ucd
• Cell Lines: 18941A-A11

Data Sources

IMPC Data for Pccb

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

cardiovascular system

hemorrhage ( J:211773 )

IMPC - UCD

embryo

spina bifida ( J:211773 )

IMPC - UCD

growth/size/body

microcephaly ( J:211773 )

IMPC - UCD

limbs/digits/tail

polydactyly ( J:211773 )

IMPC - UCD

syndactyly ( J:211773 )

IMPC - UCD

mortality/aging

preweaning lethality, complete penetrance ( J:211773 )

IMPC - UCD

nervous system

spina bifida ( J:211773 )

IMPC - UCD

vision/eye

microphthalmia ( J:211773 )

IMPC - UCD

anophthalmia ( J:211773 )

IMPC - UCD

Genotype
MGI:6461515

ht2

• Allelic Composition: Pccb^{tm1.1(KOMP)Vlcg}/Pccb⁺
• Genetic Background: C57BL/6N-Pccb^{tm1.1(KOMP)Vlcg}/Ucd
• Cell Lines: 18941A-A11

Data Sources

IMPC Data for Pccb

cardiovascular system

hemorrhage ( J:211773 )

IMPC - UCD

embryo

spina bifida ( J:211773 )

IMPC - UCD

growth/size/body

polycystic kidney ( J:211773 )

♀

IMPC - UCD

microcephaly ( J:211773 )

IMPC - UCD

limbs/digits/tail

polydactyly ( J:211773 )

IMPC - UCD

syndactyly ( J:211773 )

IMPC - UCD

nervous system

spina bifida ( J:211773 )

IMPC - UCD

renal/urinary system

abnormal kidney morphology ( J:211773 )

♀

IMPC - UCD

polycystic kidney ( J:211773 )

♀

IMPC - UCD

vision/eye

microphthalmia ( J:211773 )

IMPC - UCD

anophthalmia ( J:211773 )

IMPC - UCD