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  3. MYO9B
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Hereditary neuropathy

Gene: MYO9B

No list
MYO9B (myosin IXB)
EnsemblGeneIds (GRCh38): ENSG00000099331
EnsemblGeneIds (GRCh37): ENSG00000099331
OMIM: 602129, Gene2Phenotype
MYO9B is in 3 panels

1 review

Dmitrijs Rots (Children's Clinical University Hospital)

Green List (high evidence)

2 families with 4 affected cases + functional studies reported in 36260368
Sources: Literature
Created: 7 May 2023, 7:18 a.m.

Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal

Phenotypes
CMT2

Publications

Created: 7 May 2023, 7:18 a.m.

Panel version: 1.466

Details

Mode of Inheritance
BIALLELIC, autosomal or pseudoautosomal
Sources
Phenotypes
  • CMT2
OMIM
602129
Clinvar variants
Variants in MYO9B
Penetrance
Complete
Publications
Panels with this gene

History Filter Activity

7 May 2023, Gel status: 0

Created, Added New Source, Set mode of inheritance, Set publications, Set Phenotypes, Set penetrance

Dmitrijs Rots (Children's Clinical University Hospital)

gene: MYO9B was added gene: MYO9B was added to Hereditary neuropathy. Sources: Literature Mode of inheritance for gene: MYO9B was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: MYO9B were set to 36260368 Phenotypes for gene: MYO9B were set to CMT2 Penetrance for gene: MYO9B were set to Complete Review for gene: MYO9B was set to GREEN