Intestinal failure or congenital diarrhoea

Gene: MYO5B

Green List (high evidence)

MYO5B (myosin VB)
EnsemblGeneIds (GRCh38): ENSG00000167306
EnsemblGeneIds (GRCh37): ENSG00000167306
OMIM: 606540, Gene2Phenotype
MYO5B is in 10 panels

3 reviews

Eleanor Williams (Genomics England Curator)

This gene has been confirmed for this panel by the NHS Genomic Medicine Service and should be rated green.
Created: 8 Mar 2022, 11:44 a.m. | Last Modified: 8 Mar 2022, 11:44 a.m.
Panel Version: 1.48

Anna de Burca (Genomics England Curator)

Green List (high evidence)

PMID:29266534 summarises 62 unique 'mutations' in MYO5B (although at least one of those described has an allele frequency in ExAC of 0.3420, and thus is more likely to represent a polymorphism than a pathogenic variant). PMID: 24014347 reports a database of pathogenic variants, containing 41 variants at the time of publication. These 41 variants are included in the 62 reviewed in PMID:29266534. 15 of the 41 variants are apparently monoallelic, however the text suggests a digenic mechanism to account for this finding, rather than dominant inheritance. PMID:29266534 also reports functional evidence from cell studies and animal models that indicates that loss of function of MYO5B is associated with microvillus dysfunction and features of microvillus inclusion disease.
Created: 14 Jan 2019, 7:24 a.m.

Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal

Phenotypes
Microvillus inclusion disease

Publications

Ivone Leong (Genomics England Curator)

Green List (high evidence)

Comment when marking as ready: As discussed in the GMS Gastrohepatology Specialist Test Group webex call 14th Jan 2019: The Specialist Test Group agreed that there is enough evidence to rate this gene green.
Created: 24 Jan 2019, 4:36 p.m.
Initial gene list and info collated by Miranda Durkie Sheffield Diagnostic Genetics Service December 2018 on behalf of the GMS Gastrohepatology specialist test group. Gene Symbol submitted: MYO5B; Suggested intial gene rating: Green; Evidence for inclusion: none given; Evidence for exclusion: none given; Technical notes (e.g. non-coding/CNV mutations requiring coverage?): none given
Created: 8 Jan 2019, 10:52 a.m.

Details

Mode of Inheritance
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • NHS GMS
Phenotypes
  • Diarrhea 2, with microvillus atrophy, OMIM:251850
OMIM
606540
Clinvar variants
Variants in MYO5B
Penetrance
None
Publications
Panels with this gene

History Filter Activity

6 Jan 2022, Gel status: 3

Set Phenotypes

Arina Puzriakova (Genomics England Curator)

Phenotypes for gene: MYO5B were changed from Microvillus inclusion disease, OMIM:251850 to Diarrhea 2, with microvillus atrophy, OMIM:251850

12 Apr 2021, Gel status: 3

Set Phenotypes

Ivone Leong (Genomics England Curator)

Phenotypes for gene: MYO5B were changed from Microvillus inclusion disease, 251850 to Microvillus inclusion disease, OMIM:251850

24 Jan 2019, Gel status: 4

Entity classified by Genomics England curator

Ivone Leong (Genomics England Curator)

Gene: myo5b has been classified as Green List (High Evidence).

14 Jan 2019, Gel status: 4

Set Phenotypes

Ivone Leong (Genomics England Curator)

Phenotypes for gene: MYO5B were changed from to Microvillus inclusion disease, 251850

14 Jan 2019, Gel status: 4

Set mode of inheritance

Ivone Leong (Genomics England Curator)

Mode of inheritance for gene: MYO5B was changed from to BIALLELIC, autosomal or pseudoautosomal

14 Jan 2019, Gel status: 4

Set publications

Ivone Leong (Genomics England Curator)

Publications for gene: MYO5B were set to

8 Jan 2019, Gel status: 3

Added New Source, Status Update

Ivone Leong (Genomics England Curator)

Source Expert Review Green was added to MYO5B. Rating Changed from Red List (low evidence) to Green List (high evidence)

8 Jan 2019, Gel status: 1

Created, Added New Source, Set mode of inheritance

Ivone Leong (Genomics England Curator)

gene: MYO5B was added gene: MYO5B was added to Intestinal failure. Sources: NHS GMS Mode of inheritance for gene: MYO5B was set to