Austin-Tse et al., 2013 - Zebrafish Ciliopathy Screen Plus Human Mutational Analysis Identifies C21orf59 and CCDC65 Defects as Causing Primary Ciliary Dyskinesia. American journal of human genetics   93(4):672-686 Full text @ Am. J. Hum. Genet.
12 Genes / Markers
Marker Type Symbol Name
Gene arl13b ADP-ribosylation factor-like 13b
Gene ccdc65 coiled-coil domain containing 65
Gene cfap161 cilia and flagella associated protein 161
Gene cfap298 cilia and flagella associated protein 298
Gene foxj1a forkhead box J1a
Gene iqub IQ motif and ubiquitin domain containing
Gene lrrc23 leucine rich repeat containing 23
Gene mns1 meiosis-specific nuclear structural 1
Gene odad1 outer dynein arm docking complex subunit 1
Gene spag6 sperm associated antigen 6
Gene ubb ubiquitin B
Gene ube2kb ubiquitin-conjugating enzyme E2Kb (UBC1 homolog, yeast)
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