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Hcn2tm1.1Lex
Targeted Allele Detail
Summary
Symbol: Hcn2tm1.1Lex
Name: hyperpolarization-activated, cyclic nucleotide-gated K+ 2; targeted mutation 1.1, Lexicon Genetics
MGI ID: MGI:5295434
Synonyms: fHCN2+
Gene: Hcn2  Location: Chr10:79552468-79571942 bp, + strand  Genetic Position: Chr10, 39.72 cM, cytoband C1
Alliance: Hcn2tm1.1Lex page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:176663
Parent Cell Line:  Not Specified (ES Cell)
Strain of Origin:  Not Specified
Project Collection: Lexicon
Mutation
description
Allele Type:    Targeted (Conditional ready, No functional change)
Mutation:    Insertion
 
Mutation detailsA loxP site was inserted upstream of exon 2. An FRT-flanked neo cassette with a 3' loxP site was inserted downstream of exon 3. Flp-mediated recombination removed the neo cassette and left exons 2 and 3 floxed. (J:176663)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 0 strains available      Cell Lines: 0 lines available
Carrying any Hcn2 Mutation:  29 strains or lines available
References
Original:  J:176663 Emery EC, et al., HCN2 ion channels play a central role in inflammatory and neuropathic pain. Science. 2011 Sep 9;333(6048):1462-6
All:  2 reference(s)

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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last database update
04/23/2024
MGI 6.23
The Jackson Laboratory