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Mendeliome

Gene: CHI3L1

Red List (low evidence)

CHI3L1 (chitinase 3 like 1)
EnsemblGeneIds (GRCh38): ENSG00000133048
EnsemblGeneIds (GRCh37): ENSG00000133048
OMIM: 601525, Gene2Phenotype
CHI3L1 is in 1 panel

2 reviews

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Red List (low evidence)

Cannot find evidence for association with Mendelian disease.
Created: 3 Aug 2020, 11:32 p.m. | Last Modified: 3 Aug 2020, 11:32 p.m.
Panel Version: 0.3670

Phenotypes
{Asthma-related traits, susceptibility to, 7} 611960; {Schizophrenia, susceptibility to} 181500

Chloe Stutterd (Victorian Clinical Genetics Services)

Red List (low evidence)

Details

Mode of Inheritance
Unknown
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
Phenotypes
  • {Asthma-related traits, susceptibility to, 7} 611960
  • {Schizophrenia, susceptibility to} 181500
OMIM
601525
Clinvar variants
Variants in CHI3L1
Penetrance
None
Panels with this gene

History Filter Activity

3 Aug 2020, Gel status: 1

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Gene: chi3l1 has been classified as Red List (Low Evidence).

3 Aug 2020, Gel status: 1

Set Phenotypes

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Phenotypes for gene: CHI3L1 were changed from to {Asthma-related traits, susceptibility to, 7} 611960; {Schizophrenia, susceptibility to} 181500

3 Aug 2020, Gel status: 1

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Gene: chi3l1 has been classified as Red List (Low Evidence).

17 Nov 2019, Gel status: 3

Created, Added New Source, Set mode of inheritance

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

gene: CHI3L1 was added gene: CHI3L1 was added to Mendeliome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services Mode of inheritance for gene: CHI3L1 was set to Unknown