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P4htmtm1Soin
Targeted Allele Detail
Summary
Symbol: P4htmtm1Soin
Name: prolyl 4-hydroxylase, transmembrane (endoplasmic reticulum); targeted mutation 1, Raija Soininen
MGI ID: MGI:6342508
Gene: P4htm  Location: Chr9:108456061-108474866 bp, - strand  Genetic Position: Chr9, 59.52 cM
Alliance: P4htmtm1Soin page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:237953
Parent Cell Line:  W4 (ES Cell)
Strain of Origin:  129S6/SvEvTac
Mutation
description
Allele Type:    Targeted (Null/knockout, Reporter)
Mutation:    Insertion
    A lacZ/neo cassette was inserted into exon 3 of the gene. (J:237953)
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 P4htm Mutation:  70 strains or lines available
References
Original:  J:237953 Leinonen H, et al., Lack of P4H-TM in mice results in age-related retinal and renal alterations. Hum Mol Genet. 2016 Sep 01;25(17):3810-3823
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
05/21/2024
MGI 6.23
The Jackson Laboratory