Phenotypes associated with this allele

• Allele Symbol: Lgi4^{tm1.1(KOMP)Vlcg}
• Allele Name: targeted mutation 1.1, Velocigene
• Allele ID: MGI:5695950
• Summary: 2 genotypes

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	Lgi4^tm1.1(KOMP)Vlcg/Lgi4^tm1.1(KOMP)Vlcg	C57BL/6N-Lgi4^tm1.1(KOMP)Vlcg/Ucd	MGI:5767713
ht2	Lgi4^tm1.1(KOMP)Vlcg/Lgi4^+	C57BL/6N-Lgi4^tm1.1(KOMP)Vlcg/Ucd	MGI:5887433

Genotype
MGI:5767713

hm1

• Allelic Composition: Lgi4^{tm1.1(KOMP)Vlcg}/Lgi4^{tm1.1(KOMP)Vlcg}
• Genetic Background: C57BL/6N-Lgi4^{tm1.1(KOMP)Vlcg}/Ucd
• Cell Lines: 17152A-C10

Data Sources

IMPC Data for Lgi4

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

craniofacial

abnormal craniofacial morphology ( J:211773 )

IMPC - UCD

abnormal facial morphology ( J:211773 )

IMPC - UCD

growth/size/body

abnormal facial morphology ( J:211773 )

IMPC - UCD

mortality/aging

preweaning lethality, complete penetrance ( J:211773 )

IMPC - UCD

vision/eye

microphthalmia ( J:211773 )

IMPC - UCD

Genotype
MGI:5887433

ht2

• Allelic Composition: Lgi4^{tm1.1(KOMP)Vlcg}/Lgi4⁺
• Genetic Background: C57BL/6N-Lgi4^{tm1.1(KOMP)Vlcg}/Ucd
• Cell Lines: 17152A-C10

Data Sources

IMPC Data for Lgi4

behavior/neurological

abnormal behavior ( J:211773 )

♀

IMPC - UCD

decreased thigmotaxis ( J:211773 )

♀

IMPC - UCD

hyperactivity ( J:211773 )

♀

IMPC - UCD