Symbol
Name
ID

Ercc2
excision repair cross-complementing rodent repair deficiency, complementation group 2
MGI:95413

Phenotype annotations related to skeleton

*	Aspects of the system are reported to show a normal phenotype.
	Darker colors indicate more annotations

Human Phenotypes

Craniofacial hyperostosis

Micrognathia

Retrognathia

Microcephaly

Camptodactyly of finger

Rocker bottom foot

Pterygium

Flexion contracture

Delayed skeletal maturation

Bone pain

Pathologic fracture

Kyphoscoliosis

Vertebral compression fracture

Back pain

Osteopenia

Osteoporosis

Gout

Disease(s) Associated with ERCC2

cerebrooculofacioskeletal syndrome 2

coronary artery disease

multiple myeloma

pancreatic cancer

photosensitive trichothiodystrophy 1

xeroderma pigmentosum

xeroderma pigmentosum group D

Mouse Phenotypes		skeleton phenotype	abnormal skeleton morphology	kyphosis	decreased bone mineral density	osteoporosis
Availability	Mouse Genotype	skeleton phenotype	abnormal skeleton morphology	kyphosis	decreased bone mineral density	osteoporosis
	Ercc2^{tm2(ERCC2)Jhjh}/Ercc2^{tm2(ERCC2)Jhjh}
	Ercc2^{tm2(ERCC2)Jhjh}/Ercc2^tm2Jmch	*

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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