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Symbol
Name
ID

Pycr2
pyrroline-5-carboxylate reductase family, member 2
MGI:1277956

Phenotype annotations related to skeleton

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

Human Phenotypes	Malar flattening	Secondary microcephaly	Arachnodactyly
Disease(s) Associated with PYCR2
hypomyelinating leukodystrophy 10

Mouse Phenotypes		skeleton phenotype	kyphosis	decreased bone mineral density
Availability	Mouse Genotype	skeleton phenotype	kyphosis	decreased bone mineral density
	Pycr2^m1J/Pycr2^m1J Pycr2^m1J/Pycr2^m1J	*
	Pycr2^tm1.1Brre/Pycr2^tm1.1Brre
	Pycr2^{tm1a(EUCOMM)Wtsi}/Pycr2^{tm1a(EUCOMM)Wtsi}

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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