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  3. ZMYND10
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Rare multisystem ciliopathy disorders

Gene: ZMYND10

Red List (low evidence)
ZMYND10 (zinc finger MYND-type containing 10)
EnsemblGeneIds (GRCh38): ENSG00000004838
EnsemblGeneIds (GRCh37): ENSG00000004838
OMIM: 607070, Gene2Phenotype
ZMYND10 is in 6 panels

1 review

Alice Gardham (Genomics England)

Comment when marking as ready: Primary ciliary dyskinesia is not included in this panel
Created: 23 Jan 2017, 4:05 p.m.
Created: 23 Jan 2017, 4:05 p.m.

Panel version: 0.430

Details

Mode of Inheritance
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Radboud University Medical Center, Nijmegen
  • Expert list
Phenotypes
  • Ciliary dyskinesia, primary, 22, 615444
OMIM
607070
Clinvar variants
Variants in ZMYND10
Penetrance
Complete
Panels with this gene

History Filter Activity

26 Jan 2017, Gel status: 1

panel promoted to version 1

Alice Gardham (Genomics England)

Promoted to version 1 by Alice Gardham on 26th January 2017

23 Jan 2017, Gel status: 1

Gene classified by Genomics England curator

Alice Gardham (Genomics England)

This gene has been classified as Red List (Low Evidence).

25 Nov 2016, Gel status: 1

Upload gene information

Ellen McDonagh (Genomics England Curator)

ZMYND10 was added to Rare multisystem ciliopathy disorderspanel. Sources: Radboud University Medical Center, Nijmegen

25 Nov 2016, Gel status: 0

Set Phenotypes

Ellen McDonagh (Genomics England Curator)

Phenotypes for gene ZMYND10 were set to Ciliary dyskinesia, primary, 22, 615444

5 Apr 2016, Gel status: 0

Created

Ellen McDonagh (Genomics England Curator)

ZMYND10 was created by ellenmcdonagh

5 Apr 2016, Gel status: 0

Added New Source

Ellen McDonagh (Genomics England Curator)

ZMYND10 was added to Rare multisystem ciliopathy disorderspanel. Sources: Expert list