Ccdc9b | coiled-coil domain containing 9B

GeneMGI:2685199Synonyms: A430105I19Rik

Physiological systems

17 / 24 physiological systems tested

2 Significantly impacted by the knock-out

 Nervous system Behavior/neurological

15 No significant impact

7 Not tested

Gene metrics:2Significant phenotypes
0Associated diseases
Expression examined in:0Adult tissues
0Embryo tissues

Phenotypes

decreased exploration in new environment1 supporting datasetCcdc9bem1(IMPC)TcphomozygoteEarly adult2.13x10-6 
decreased prepulse inhibition4 supporting datasetsCcdc9bem1(IMPC)TcphomozygoteEarly adult1.89x10-11 
* Does not have a P-value assigned because it was manually marked as significant.
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* This parameter was manually assessed for significance.
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lacZ Expression

Human diseases caused by Ccdc9b mutations

The analysis uses data from IMPC, along with published data on other mouse mutants, in comparison to human disease reports in OMIM, Orphanet, and DECIPHER.

Phenotype comparisons summarize the similarity of mouse phenotypes with human disease phenotypes.






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Histopathology

IMPC related publications

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Ccdc9bem1(IMPC)TcpIntra-exon deletionmouse
Ccdc9btm1a(KOMP)MbpKO first allele (reporter-tagged insertion with conditional potential)targeting vector
ES Cell
Ccdc9btm1e(EUCOMM)WtsiTargeted, non-conditional alleleES Cell
Ccdc9btm1e(KOMP)MbpTargeted, non-conditional alleleES Cell
Ccdc9btm2a(KOMP)MbpKO first allele (reporter-tagged insertion with conditional potential)targeting vector
ES Cell
Ccdc9btm2e(KOMP)MbpTargeted, non-conditional alleleES Cell
Ccdc9btm48187(L1L2_Bact_P)KO first allele (reporter-tagged insertion with conditional potential)targeting vector

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