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Symbol
Name
ID

Ercc1
excision repair cross-complementing rodent repair deficiency, complementation group 1
MGI:95412

Phenotype annotations related to nervous system

Darker colors indicate more annotations

Human Phenotypes	Microcephaly	Anorexia	Polymicrogyria	Simplified gyral pattern	Cerebellar hypoplasia	Spinal cord compression	EEG abnormality	Hyperreflexia	Brisk reflexes	Global developmental delay	Paresthesia
Disease(s) Associated with ERCC1	Microcephaly	Anorexia	Polymicrogyria	Simplified gyral pattern	Cerebellar hypoplasia	Spinal cord compression	EEG abnormality	Hyperreflexia	Brisk reflexes	Global developmental delay	Paresthesia
cerebrooculofacioskeletal syndrome 4
multiple myeloma
pancreatic cancer

Mouse Phenotypes		cochlear hair cell degeneration
Availability	Mouse Genotype	cochlear hair cell degeneration
	Ercc1^tm1Jhjh/Ercc1^tm2Jhjh

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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