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Search results 1 to 14 out of 14 for Ccdc151

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Categories

Hits by Category

Type Details Score
Protein
A0A0R4J1K3
Organism: Mus musculus/domesticus
Length: 594  
Fragment?: false
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Publication
25192045 | J:215900
First Author: Hjeij R
Year: 2014
Journal: Am J Hum Genet
Title: CCDC151 mutations cause primary ciliary dyskinesia by disruption of the outer dynein arm docking complex formation.
Volume: 95
Issue: 3
Pages: 257-74
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Publication
24067530 | J:215963
First Author: Jerber J
Year: 2014
Journal: Hum Mol Genet
Title: The coiled-coil domain containing protein CCDC151 is required for the function of IFT-dependent motile cilia in animals.
Volume: 23
Issue: 3
Pages: 563-77
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Protein
Q8BSN3
Organism: Mus musculus/domesticus
Length: 593  
Fragment?: false
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Protein
Q8BSN3-3
Organism: Mus musculus/domesticus
Length: 594  
Fragment?: false
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Protein
Q8BSN3-2
Organism: Mus musculus/domesticus
Length: 166  
Fragment?: false
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Protein Coding Gene
MGI:1924859 | Odad3
Type: protein_coding_gene
Organism: mouse, laboratory
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Gene
115948 | ODAD3
Type: gene
Organism: human
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Allele
Odad3<tm1b(EUCOMM)Hmgu> | MGI:5548687
Name: outer dynein arm docking complex subunit 3; targeted mutation 1b, Helmholtz Zentrum Muenchen GmbH
Allele Type: Targeted
Attribute String: Null/knockout, Reporter
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Allele
Odad3<b2b1885Clo> | MGI:5445347
 
Name: outer dynein arm docking complex subunit 3; Bench to Bassinet Program (B2B/CVDC), mutation 1885 Cecilia Lo
Allele Type: Chemically induced (ENU)
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DO Term
DOID:0110624 | primary ciliary dyskinesia 30
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Genotype
Genotype
Symbol: Odad3/Odad3
Background: C57BL/6N-Odad3/Cnrm
Zygosity: hm
Has Mutant Allele: true
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Genotype
Genotype
Symbol: Odad3/Odad3
Background: C57BL/6J-Odad3
Zygosity: hm
Has Mutant Allele: true
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Publication
31383820 | J:278798
 
First Author: Chiani F
Year: 2019
Journal: Dis Model Mech
Title: Functional loss of Ccdc1 51 leads to hydrocephalus in a mouse model of primary ciliary dyskinesia.
Volume: 12
Issue: 8
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