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Table 1 Green genes on the primary ciliary disorders PanelApp virtual gene panel, considered diagnostic for PCD in the clinical analysis pipeline of the 100,000 Genomes Project

From: Whole genome sequencing in the diagnosis of primary ciliary dyskinesia

Gene Name

Model_Of_Inheritance

OMIM number

ARMC4

Autosomal recessive

615451

C21orf59

Autosomal recessive

615500

CCDC103

Autosomal recessive

614679

CCDC114

Autosomal recessive

615067

CCDC151

Autosomal recessive

616037

CCDC39

Autosomal recessive

613807

CCDC40

Autosomal recessive

613808

CCDC65

Autosomal recessive

615504

CCNO

Autosomal recessive

615872

DNAAF1

Autosomal recessive

613193

DNAAF2

Autosomal recessive

612518

DNAAF3

Autosomal recessive

606763

DNAAF4

Autosomal recessive

127700

DNAAF5

Autosomal recessive

614874

DNAH11

Autosomal recessive

611884

DNAH5

Autosomal recessive

608644

DNAI1

Autosomal recessive

244400

DNAI2

Autosomal recessive

612444

DNAL1

Autosomal recessive

614017

DRC1

Autosomal recessive

615294

GAS8

Autosomal recessive

616726

HYDIN

Autosomal recessive

608647

LRRC6

Autosomal recessive

614935

MCIDAS

Autosomal recessive

618695

PIH1D3

X-linked recessive

300991

RPGR

X-linked recessive

300455

RSPH1

Autosomal recessive

615481

RSPH3

Autosomal recessive

616481

RSPH4A

Autosomal recessive

612649

RSPH9

Autosomal recessive

612650

SPAG1

Autosomal recessive

615505

ZMYND10

Autosomal recessive

615444

  1. Gene name, pattern of inheritance and OMIM ID are provided for each gene. This panel was originally 31 genes at the start of the project; PIH1D3 was added towards the end of the project. All PCD patients had this panel applied. Some but not all non-CF bronchiectasis patients had this panel applied