C3.OH-H2<o2> Slc22a5<jvs> Strain Detail MGI Mouse MGI:2164427

C3.OH-H2^o2 Slc22a5^jvs Strain Detail

Summary

Strain Name

C3.OH-H2^o2 Slc22a5^jvs
Attributes

coisogenic, congenic, major histocompatibility congenic, mutant strain, spontaneous mutation
MGI ID

MGI:2164427
Synonyms

C3.OH-H2^o2-Slc22a5^jvs/Slc22a5^jvs

2 associated mutations

Mutation Carried	Marker
	H2
Slc22a5^jvs	Slc22a5

Phenotype Overview

Blue squares indicate phenotypes directly attributed to mutations/alleles in this strain.

adipose tissue	behavior/neurological	cardiovascular system	cellular	craniofacial	digestive/alimentary system	embryo	endocrine/exocrine glands	growth/size/body	hearing/vestibular/ear	hematopoietic system	homeostasis/metabolism	immune system	integument	limbs/digits/tail	liver/biliary system	mortality/aging	muscle	neoplasm	nervous system	normal phenotype	pigmentation	renal/urinary system	reproductive system	respiratory system	skeleton	taste/olfaction	vision/eye

Click cells to view annotations.

Human Diseases

	model 1
systemic primary carnitine deficiency disease	√

Key

√

disease model

expected model not found

Earliest

J:51918 Nezu J, et al., Primary systemic carnitine deficiency is caused by mutations in a gene encoding sodium ion-dependent carnitine transporter. Nat Genet. 1999 Jan;21(1):91-4
All

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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