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Kctd19em1Fcw
Endonuclease-mediated Allele Detail
Summary
Symbol: Kctd19em1Fcw
Name: potassium channel tetramerisation domain containing 19; endonuclease-mediated mutation 1, Fengchao Wang
MGI ID: MGI:7511806
Gene: Kctd19  Location: Chr8:106109439-106140134 bp, - strand  Genetic Position: Chr8, 53.04 cM
Alliance: Kctd19em1Fcw page
Mutation
origin
Strain of Origin:  Not Specified
Mutation
description
Allele Type:    Endonuclease-mediated (Null/knockout)
Mutation:    Intragenic deletion
 
Mutation detailsCRISPR/Cas9 technology generated a 104-bp deletion within exon 2. Western blot analysis confirmed absence of protein in homozygotes. (J:338159)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 1 anatomical structure(s)
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 Kctd19 Mutation:  52 strains or lines available
References
Original:  J:338159 Li Y, et al., The ZFP541-KCTD19 complex is essential for pachytene progression by activating meiotic genes during mouse spermatogenesis. J Genet Genomics. 2022 Nov;49(11):1029-1041
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
10/29/2024
MGI 6.24
The Jackson Laboratory