Mouse Genome Informatics
hm1
    Arhgap6/Hccs/Mid1tm1Hzo/Arhgap6/Hccs/Mid1tm1Hzo
involves: 129S7/SvEvBrd
Key:
phenotype observed in females WTSI Wellcome Trust Sanger Institute
phenotype observed in males EuPh Europhenome
N normal phenotype
normal phenotype


Mouse Genome Informatics
cn2
    Arhgap6/Hccs/Mid1tm1Hzo/Arhgap6/Hccs/Mid1tm1Hzo
Tg(EIIa-cre)C5379Lmgd/?

involves: 129S7/SvEvBrd * C57BL/6 * FVB/N
Key:
phenotype observed in females WTSI Wellcome Trust Sanger Institute
phenotype observed in males EuPh Europhenome
N normal phenotype
mortality/aging
• 15 of 21 embryos abnormal at E9.5 and E10.5 (J:80528)
• mosaic animals were present and were healthy and fertile (J:80528)
• no homozygous mice born (J:80528)

embryogenesis
• many embryos undergoing resorption by E9.5-E10.5 (J:80528)
• gastrulation defects (J:80528)

growth/size

Mouse Models of Human Disease
OMIM IDRef(s)
Microphthalmia, Syndromic 7; MCOPS7 309801 J:80528


Mouse Genome Informatics
cn3
    Arhgap6/Hccs/Mid1tm1Hzo/Y
Tg(EIIa-cre)C5379Lmgd/?

involves: 129S7/SvEvBrd * C57BL/6 * FVB/N
Key:
phenotype observed in females WTSI Wellcome Trust Sanger Institute
phenotype observed in males EuPh Europhenome
N normal phenotype
mortality/aging
• no hemizygous mice born (J:80528)
• 15 of 21 embryos abnormal at E9.5 and E10.5 (J:80528)
• mosaic animals were present and were healthy and fertile (J:80528)

embryogenesis
• many embryos undergoing resorption by E9.5-E10.5 (J:80528)
• gastrulation defects (J:80528)

growth/size

Mouse Models of Human Disease
OMIM IDRef(s)
Microphthalmia, Syndromic 7; MCOPS7 309801 J:80528


Mouse Genome Informatics
cn4
    Arhgap6/Hccs/Mid1tm1Hzo/Mid1+
Tg(EIIa-cre)C5379Lmgd/?

involves: 129S7/SvEvBrd * C57BL/6 * FVB/N
Key:
phenotype observed in females WTSI Wellcome Trust Sanger Institute
phenotype observed in males EuPh Europhenome
N normal phenotype
mortality/aging
• no heterozygotes born (J:80528)

Mouse Models of Human Disease
OMIM IDRef(s)
Microphthalmia, Syndromic 7; MCOPS7 309801 J:80528


Mouse Genome Informatics
ot5
    Arhgap6/Hccs/Mid1tm1Hzo/Y
involves: 129S7/SvEvBrd
Key:
phenotype observed in females WTSI Wellcome Trust Sanger Institute
phenotype observed in males EuPh Europhenome
N normal phenotype
normal phenotype