C57BL/6N-A<tm1Brd> Nhlrc2<tm1a(KOMP)Wtsi>/WtsiOulu Strain Detail MGI Mouse MGI:6122765

C57BL/6N-A^tm1Brd Nhlrc2^{tm1a(KOMP)Wtsi}/WtsiOulu Strain Detail

Summary

1 associated mutation

Mutation Carried	Marker
Nhlrc2^{tm1a(KOMP)Wtsi}	Nhlrc2

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.

1 associated strain record at IMSR

IMSR	Repository	IMSR Strain	Why Matched
EM:10219	EMMA	C57BL/6N-A^tm1Brd Nhlrc2^{tm1a(KOMP)Wtsi}/WtsiOulu	exact match to ID

Earliest

J:267291 Paakkola T, et al., Biallelic mutations in human NHLRC2 enhance myofibroblast differentiation in FINCA disease. Hum Mol Genet. 2018 Dec 15;27(24):4288-4302
All

4

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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