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Prepair 1000+

Gene: SGO1

Red List (low evidence)

SGO1 (shugoshin 1)
EnsemblGeneIds (GRCh38): ENSG00000129810
EnsemblGeneIds (GRCh37): ENSG00000129810
OMIM: 609168, Gene2Phenotype
SGO1 is in 4 panels

2 reviews

Cassandra Muller (Victorian Clinical Genetics Services)

Red List (low evidence)

No further evidence found since previous review
Created: 7 Feb 2025, 1:15 a.m. | Last Modified: 7 Feb 2025, 1:15 a.m.
Panel Version: 1.1460

Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal

Phenotypes
Chronic atrial and intestinal dysrhythmia, 616201 (3)

Crystle Lee (Victorian Clinical Genetics Services)

Red List (low evidence)

Insufficient evidence for inclusion. No additional supporting evidence identified

Single homozygous missense identified in 15 individuals, founder effect demonstrated by haplotype analysis.
Created: 11 Jul 2022, 7:08 a.m. | Last Modified: 11 Jul 2022, 7:08 a.m.
Panel Version: 0.31

Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal

Phenotypes
Chronic atrial and intestinal dysrhythmia, MIM# 616201

Publications

Details

Mode of Inheritance
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Mackenzie's Mission
Phenotypes
  • Chronic atrial and intestinal dysrhythmia, 616201 (3)
Tags
founder
OMIM
609168
Clinvar variants
Variants in SGO1
Penetrance
None
Publications
Panels with this gene

History Filter Activity

13 Jul 2022, Gel status: 1

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Gene: sgo1 has been classified as Red List (Low Evidence).

13 Jul 2022, Gel status: 1

Set publications

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Publications for gene: SGO1 were set to

13 Jul 2022, Gel status: 1

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Gene: sgo1 has been classified as Red List (Low Evidence).

13 Jul 2022, Gel status: 3

Added Tag

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Tag founder tag was added to gene: SGO1.

1 Jun 2022, Gel status: 3

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

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

gene: SGO1 was added gene: SGO1 was added to Reproductive Carrier Screen_VCGS. Sources: Mackenzie's Mission,Expert Review Green Mode of inheritance for gene: SGO1 was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: SGO1 were set to Chronic atrial and intestinal dysrhythmia, 616201 (3)