Phenotypes Associated with This Genotype

Genotype
MGI:5700836

• Allelic Composition: Chst11^{tm1a(KOMP)Wtsi}/Chst11^{tm1a(KOMP)Wtsi}
• Genetic Background: C57BL/6N-Chst11^{tm1a(KOMP)Wtsi}/Wtsi
• Cell Lines: EPD0293_6_C11

Data Sources

IMPC Data for Chst11

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

cardiovascular system

abnormal vertebral artery topology ( J:239583 )

DMDD

additional anastomosis between intracranial vertebral arteries ( J:239583 )

DMDD

cerebral arteriovenous malformation ( J:239583 )

DMDD

umbilical vein stenosis ( J:239583 )

DMDD

abnormal vitelline vein connection ( J:239583 )

DMDD

abnormal vitelline vein topology ( J:239583 )

DMDD

ductus venosus stenosis ( J:239583 )

DMDD

hepatic portal vein stenosis ( J:239583 )

DMDD

bicuspid aortic valve ( J:239583 )

DMDD

craniofacial

cleft palate ( J:239583 )

DMDD

digestive/alimentary system

cleft palate ( J:239583 )

DMDD

embryo

umbilical vein stenosis ( J:239583 )

DMDD

abnormal vitelline vein connection ( J:239583 )

DMDD

abnormal vitelline vein topology ( J:239583 )

DMDD

abnormal Mullerian duct morphology ( J:239583 )

DMDD

embryo cyst ( J:239583 )

DMDD

endocrine/exocrine glands

abnormal thymus morphology ( J:239583 )

DMDD

growth/size/body

cleft palate ( J:239583 )

DMDD

embryo cyst ( J:239583 )

DMDD

hematopoietic system

abnormal thymus morphology ( J:239583 )

DMDD

immune system

abnormal thymus morphology ( J:239583 )

DMDD

blood in lymph vessels ( J:239583 )

DMDD

mortality/aging

preweaning lethality, complete penetrance ( J:211773 )

IMPC - WTSI

muscle

abnormal eye muscle topology ( J:239583 )

DMDD

nervous system

cerebral arteriovenous malformation ( J:239583 )

DMDD

renal/urinary system

double ureter ( J:239583 )

DMDD

skeleton

abnormal perichondrial ossification ( J:239583 )

DMDD

vision/eye

abnormal eye muscle topology ( J:239583 )

DMDD