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Kctd9em1Beij
Endonuclease-mediated Allele Detail
Summary
Symbol: Kctd9em1Beij
Name: potassium channel tetramerisation domain containing 9; endonuclease-mediated mutation 1, Chinese Academy of Sciences
MGI ID: MGI:6382731
Gene: Kctd9  Location: Chr14:67953536-67979760 bp, + strand  Genetic Position: Chr14, 34.66 cM
Alliance: Kctd9em1Beij page
Mutation
origin
Strain of Origin:  BALB/c
Mutation
description
Allele Type:    Endonuclease-mediated (Null/knockout)
Mutation:    Intragenic deletion
    TALEN-targeting removed 40 nucleotides in exon 6 and 30 nucleotides in intron 6. (J:281803)
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 Kctd9 Mutation:  24 strains or lines available
References
Original:  J:281803 Zhang X, et al., Kctd9 Deficiency Impairs Natural Killer Cell Development and Effector Function. Front Immunol. 2019;10:744
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
04/16/2024
MGI 6.23
The Jackson Laboratory