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Mendeliome

Gene: MOV10L1

Amber List (moderate evidence)

MOV10L1 (Mov10 RISC complex RNA helicase like 1)
EnsemblGeneIds (GRCh38): ENSG00000073146
EnsemblGeneIds (GRCh37): ENSG00000073146
OMIM: 605794, Gene2Phenotype
MOV10L1 is in 1 panel

1 review

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

I don't know

Two unrelated individuals and a mouse model.
Sources: Expert list
Created: 12 May 2022, 8:30 p.m.

Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal

Phenotypes
Spermatogenic failure 73, MIM#619878

Publications

Details

Mode of Inheritance
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Expert list
Phenotypes
  • Spermatogenic failure 73, MIM#619878
OMIM
605794
Clinvar variants
Variants in MOV10L1
Penetrance
None
Publications
Panels with this gene

History Filter Activity

12 May 2022, Gel status: 2

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Gene: mov10l1 has been classified as Amber List (Moderate Evidence).

12 May 2022, Gel status: 2

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Gene: mov10l1 has been classified as Amber List (Moderate Evidence).

12 May 2022, Gel status: 1

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

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

gene: MOV10L1 was added gene: MOV10L1 was added to Mendeliome. Sources: Expert list Mode of inheritance for gene: MOV10L1 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: MOV10L1 were set to 35476666; 20534472 Phenotypes for gene: MOV10L1 were set to Spermatogenic failure 73, MIM#619878 Review for gene: MOV10L1 was set to AMBER