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Intellectual disability syndromic and non-syndromic

Gene: C3orf58

Red List (low evidence)

C3orf58 (chromosome 3 open reading frame 58)
EnsemblGeneIds (GRCh38): ENSG00000181744
EnsemblGeneIds (GRCh37): ENSG00000181744
OMIM: 612200, Gene2Phenotype
C3orf58 is in 2 panels

1 review

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Red List (low evidence)

No evidence currently for Mendelian disease association.
Created: 19 Nov 2019, 11:04 a.m. | Last Modified: 19 Nov 2019, 11:04 a.m.
Panel Version: 0.4

Details

Mode of Inheritance
Unknown
Sources
  • Expert Review Red
  • Genetic Health Queensland
  • Victorian Clinical Genetics Services
OMIM
612200
Clinvar variants
Variants in C3orf58
Penetrance
None
Panels with this gene

History Filter Activity

6 Dec 2019, Gel status: 1

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Gene: c3orf58 has been classified as Red List (Low Evidence).

6 Dec 2019, Gel status: 1

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Gene: c3orf58 has been classified as Red List (Low Evidence).

22 Nov 2019, Gel status: 3

Created, Added New Source, Set mode of inheritance

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

gene: C3orf58 was added gene: C3orf58 was added to Intellectual disability, syndromic and non-syndromic_GHQ. Sources: Expert Review Green,Genetic Health Queensland Mode of inheritance for gene: C3orf58 was set to Unknown