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Symbol
Name
ID

Orc1
origin recognition complex, subunit 1
MGI:1328337

Phenotype annotations related to behavior/neurological

Darker colors indicate more annotations

Human Phenotypes	Feeding difficulties in infancy
Disease(s) Associated with ORC1	Feeding difficulties in infancy
Meier-Gorlin syndrome 1

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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