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Symbol
Name
ID
Rac1
Rac family small GTPase 1
MGI:97845
Phenotype annotations related to embryo
Darker colors indicate more annotations
Human Phenotypes
Echogenic intracardiac focus
Disease(s) Associated with RAC1
autosomal dominant intellectual developmental disorder 48

Mouse Phenotypes
increased embryonic tissue cell apoptosis
abnormal anterior visceral endoderm cell migration
abnormal developmental patterning
abnormal gastrulation
abnormal germ layer development
abnormal mesoderm development
abnormal rostral-caudal axis patterning
abnormal rostral-caudal body axis extension
embryonic growth arrest
decreased embryo size
abnormal embryonic epiblast morphology
thick embryonic epiblast
abnormal notochordal plate morphology
absent mesoderm
abnormal neural tube closure
abnormal primitive streak morphology
abnormal primitive node morphology
abnormal primitive streak formation
impaired somite development
absent somites
abnormal embryonic-extraembryonic boundary morphology
embryonic-extraembryonic boundary constriction
abnormal extraembryonic endoderm formation
Availability Mouse Genotype
Rac1tm1Jms/Rac1tm1Jms
Rac1tm2Tyb/Rac1tm2Tyb
Rac1tm2Tyb/Rac1tm2Tyb
Tg(Hhex-EGFP)#Rbe/0
Rac1tm1Tyb/Rac1tm2Tyb
Edil3Tg(Sox2-cre)1Amc/Edil3+  (conditional)
Rac1tm1Tyb/Rac1tm2Tyb
Tg(Ttr-cre)1Hadj/0  (conditional)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
04/16/2024
MGI 6.23
The Jackson Laboratory