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Table S3: Genes tested for interaction with PIH1D3

PAFF, Tamara, et al. Mutations in PIH1D3 cause X-linked primary ciliary dyskinesia with outer and inner dynein arm defects. The American Journal of Human Genetics, 2017, 100. Jg., Nr. 1, S. 160-168.

Publication: https://doi.org/10.1016/j.ajhg.2016.11.019

Description

Abbreviations:
+: interaction observed
-: no interaction observed

Disclaimer

The publication Mutations in PIH1D3 Cause X-Linked Primary Ciliary Dyskinesia with Outer and Inner Dynein Arm Defects by Tamara Paff, Niki T.Loges, Isabella Aprea, Kaman Wu, Zeineb Bakey, Eric G. Haarman, Johannes M.A. Daniels, Erik A. Sistermans, Natalija Bogunovic, Gerard W. Dougherty, Inga M.Höben, Jörg Große-Onnebrink, Anja Matter, Heike Olbrich, Claudius Werner, Gerard Pals, Miriam Schmidts, Heymut Omran, Dimitra Micha is published under an open access no derivatives license: : https://creativecommons.org/licenses/by-nc-nd/4.0/. Granted rights: share — copy and redistribute the material in any medium or format. No alterations allowed. Thus, tables can not be shown in MFGA format.

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Table

GENE InteractionWithPih1d3
CCDC103 -
CCDC114 -
CCDC151 -
C21orf59 -
DNAAF1 -
DNAAF2 +
DNAAF3 -
DNAAF4 +
DNAH11 -
DNAI1 -
DNALI1 -
HSP90 +
IFT46 -
LRRC6 -
TTC25 -
TXNDC3 -
WDR69 -
ZMYND10 -