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Egln1tm4.1(EGLN1*)Fsl
Targeted Allele Detail
Summary
Symbol: Egln1tm4.1(EGLN1*)Fsl
Name: egl-9 family hypoxia-inducible factor 1; targeted mutation 4.1,Frank Lee
MGI ID: MGI:8186458
Synonyms: Phd2Tib
Gene: Egln1  Location: Chr8:125635326-125676063 bp, - strand  Genetic Position: Chr8, 72.86 cM
Alliance: Egln1tm4.1(EGLN1*)Fsl page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:289921
Parent Cell Line:  EAP6 (ES Cell)
Strain of Origin:  C57BL/6
Mutation
description
Allele Type:    Targeted (Humanized sequence, Inserted expressed sequence)
Mutation:    Insertion
 
Egln1tm4.1(EGLN1*)Fsl expresses 1 gene
 
Mutation detailsThe targeting vector was designed to replace the endogenous exon 1 of the egl-9 family hypoxia-inducible factor 1 (Egln1) gene with a human exon 1 sequence that harbors a D4E/C127S double amino acid substitution. The targeting construct also consisted of a loxP-flanked neomycin selection cassette. The the floxed neomycin cassette was removed by Cre recombinase. (J:289921)
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 1 strain available      Cell Lines: 0 lines available
Carrying any Egln1 Mutation:  23 strains or lines available
References
Original:  J:289921 Song D, et al., Tibetan PHD2, an allele with loss-of-function properties. Proc Natl Acad Sci U S A. 2020 Jun 2;117(22):12230-12238
All:  1 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
07/29/2025
MGI 6.24
The Jackson Laboratory