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Symbol
Name
ID

Ercc8
excision repaiross-complementing rodent repair deficiency, complementation group 8
MGI:1919241

Phenotype annotations related to behavior/neurological

Darker colors indicate more annotations

Human Phenotypes	Feeding difficulties in infancy	Gastrostomy tube feeding in infancy	Photophobia	Urinary incontinence	Atypical behavior	Weak cry
Disease(s) Associated with ERCC8	Feeding difficulties in infancy	Gastrostomy tube feeding in infancy	Photophobia	Urinary incontinence	Atypical behavior	Weak cry
Cockayne syndrome
Cockayne syndrome A

Mouse Phenotypes		photophobia	abnormal locomotor behavior
Availability	Mouse Genotype	photophobia	abnormal locomotor behavior
	Ercc8^em1(IMPC)H/Ercc8^em1(IMPC)H
	Ercc8^tm1Jhjh/Ercc8^tm1Jhjh

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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