Phenotypes associated with this allele

• Allele Symbol: D930028M14Rik^{tm1a(EUCOMM)Wtsi}
• Allele Name: targeted mutation 1a, Wellcome Trust Sanger Institute
• Allele ID: MGI:4432198
• Summary: 1 genotype

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	D930028M14Rik^tm1a(EUCOMM)Wtsi/D930028M14Rik^tm1a(EUCOMM)Wtsi	C57BL/6N-D930028M14Rik^tm1a(EUCOMM)Wtsi/Wtsi	MGI:5767622

Genotype
MGI:5767622

hm1

• Allelic Composition: D930028M14Rik^{tm1a(EUCOMM)Wtsi}/D930028M14Rik^{tm1a(EUCOMM)Wtsi}
• Genetic Background: C57BL/6N-D930028M14Rik^{tm1a(EUCOMM)Wtsi}/Wtsi
• Cell Lines: EPD0289_2_A05

Data Sources

IMPC Data for D930028M14Rik

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

cardiovascular system

umbilical vein stenosis ( J:239583 )

DMDD

abnormal pulmonary valve cusp morphology ( J:239583 )

DMDD

craniofacial

absent hypoglossal canal ( J:239583 )

DMDD

embryo

umbilical vein stenosis ( J:239583 )

DMDD

homeostasis/metabolism

retropleural edema ( J:239583 )

DMDD

liver/biliary system

herniated liver ( J:239583 )

DMDD

mortality/aging

preweaning lethality, complete penetrance ( J:211773 )

IMPC - WTSI

muscle

abnormal eye muscle morphology ( J:239583 )

DMDD

nervous system

abnormal brachial plexus formation ( J:239583 )

DMDD

absent abducens nerve ( J:239583 )

DMDD

abnormal hypoglossal nerve topology ( J:239583 )

DMDD

absent hypoglossal nerve ( J:239583 )

DMDD

vagus nerve compression ( J:239583 )

DMDD

skeleton

absent hypoglossal canal ( J:239583 )

DMDD

vision/eye

abnormal eye muscle morphology ( J:239583 )

DMDD