Phenotypes associated with this allele

• Allele Symbol: Snx3^{tm1.1(KOMP)Vlcg}
• Allele Name: targeted mutation 1.1, Velocigene
• Allele ID: MGI:5634800
• Summary: 2 genotypes

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	Snx3^tm1.1(KOMP)Vlcg/Snx3^tm1.1(KOMP)Vlcg	C57BL/6N-Snx3^tm1.1(KOMP)Vlcg/J	MGI:5767809
ht2	Snx3^tm1.1(KOMP)Vlcg/Snx3^+	C57BL/6N-Snx3^tm1.1(KOMP)Vlcg/J	MGI:5888413

Genotype
MGI:5767809

hm1

• Allelic Composition: Snx3^{tm1.1(KOMP)Vlcg}/Snx3^{tm1.1(KOMP)Vlcg}
• Genetic Background: C57BL/6N-Snx3^{tm1.1(KOMP)Vlcg}/J
• Cell Lines: 15552A-B8

Data Sources

IMPC Data for Snx3

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

craniofacial

abnormal craniofacial morphology ( J:211773 )

IMPC - JAX

abnormal facial morphology ( J:211773 )

IMPC - JAX

cleft palate ( J:211773 )

IMPC - JAX

abnormal head shape ( J:211773 )

IMPC - JAX

digestive/alimentary system

cleft palate ( J:211773 )

IMPC - JAX

embryo

abnormal embryo size ( J:211773 )

IMPC - JAX

abnormal neural tube closure ( J:211773 )

IMPC - JAX

spina bifida ( J:211773 )

IMPC - JAX

growth/size/body

abnormal facial morphology ( J:211773 )

IMPC - JAX

cleft palate ( J:211773 )

IMPC - JAX

abnormal head shape ( J:211773 )

IMPC - JAX

abnormal embryo size ( J:211773 )

IMPC - JAX

homeostasis/metabolism

edema ( J:211773 )

IMPC - JAX

integument

pallor ( J:211773 )

IMPC - JAX

limbs/digits/tail

abnormal limb morphology ( J:211773 )

IMPC - JAX

syndactyly ( J:211773 )

IMPC - JAX

abnormal tail morphology ( J:211773 )

IMPC - JAX

mortality/aging

preweaning lethality, complete penetrance ( J:211773 )

IMPC - JAX

nervous system

abnormal neural tube closure ( J:211773 )

IMPC - JAX

spina bifida ( J:211773 )

IMPC - JAX

abnormal midbrain morphology ( J:211773 )

IMPC - JAX

abnormal forebrain morphology ( J:211773 )

IMPC - JAX

abnormal hindbrain morphology ( J:211773 )

IMPC - JAX

exencephaly ( J:211773 )

IMPC - JAX

vision/eye

microphthalmia ( J:211773 )

IMPC - JAX

anophthalmia ( J:211773 )

IMPC - JAX

Genotype
MGI:5888413

ht2

• Allelic Composition: Snx3^{tm1.1(KOMP)Vlcg}/Snx3⁺
• Genetic Background: C57BL/6N-Snx3^{tm1.1(KOMP)Vlcg}/J
• Cell Lines: 15552A-B8

Data Sources

IMPC Data for Snx3

homeostasis/metabolism

increased blood urea nitrogen level ( J:211773 )

♀

IMPC - JAX