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Symbol
Name
ID
Shoc2
Shoc2, leucine rich repeat scaffold protein
MGI:1927197
Phenotype annotations related to embryo
*Aspects of the system are reported to show a normal phenotype.
Darker colors indicate more annotations
Human Phenotypes
Polyhydramnios
Disease(s) Associated with SHOC2
Noonan syndrome-like disorder with loose anagen hair 1

Mouse Phenotypes
embryo phenotype
embryonic growth retardation
Availability Mouse Genotype
Shoc2tm1.1Mhan/Shoc2tm1.2Mhan
Tg(Tek-cre)#Xya/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
04/30/2024
MGI 6.23
The Jackson Laboratory