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Cyp17a1tm1Mell
Targeted Allele Detail
Summary
Symbol: Cyp17a1tm1Mell
Name: cytochrome P450, family 17, subfamily a, polypeptide 1; targeted mutation 1, Synthia H Mellon
MGI ID: MGI:3047328
Synonyms: P450c17-
Gene: Cyp17a1  Location: Chr19:46655604-46661439 bp, - strand  Genetic Position: Chr19, 38.97 cM
Alliance: Cyp17a1tm1Mell page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:91081
Parent Cell Line:  JM-1 (ES Cell)
Strain of Origin:  129X1/SvJ
Mutation
description
Allele Type:    Targeted (Null/knockout)
Mutations:    Insertion, Intragenic deletion
 
Mutation detailsPart of exon 5 and all of exon 6 were replaced with a neo. Exon 6 contains the Ozols peptide, which comprises amino acids 346 to 366 and contains amino acids crucial for redox partner binding. Immunostaining of embryos revealed absence of protein in homozygous mutants. (J:91081)
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 Cyp17a1 Mutation:  24 strains or lines available
References
Original:  J:91081 Bair SR, et al., Deletion of the mouse P450c17 gene causes early embryonic lethality. Mol Cell Biol. 2004 Jun;24(12):5383-90
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
10/29/2024
MGI 6.24
The Jackson Laboratory