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  2. Complement Deficiencies
  3. ITGAM
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Complement Deficiencies

Gene: ITGAM

Red List (low evidence)
ITGAM (integrin subunit alpha M)
EnsemblGeneIds (GRCh38): ENSG00000169896
EnsemblGeneIds (GRCh37): ENSG00000169896
OMIM: 120980, Gene2Phenotype
ITGAM is in 2 panels

1 review

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Red List (low evidence)

Cannot find association with Mendelian disease.
Created: 11 Apr 2020, 2:46 a.m. | Last Modified: 11 Apr 2020, 2:46 a.m.
Panel Version: 0.27
Created: 11 Apr 2020, 2:46 a.m.
Last Modified: 11 Apr 2020, 2:46 a.m.
Panel version: 0.27

Details

Mode of Inheritance
Unknown
Sources
  • Expert Review Red
  • Melbourne Genomics Health Alliance Immunology Flagship
  • Victorian Clinical Genetics Services
OMIM
120980
Clinvar variants
Variants in ITGAM
Penetrance
None
Panels with this gene

History Filter Activity

11 Apr 2020, Gel status: 1

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

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

11 Apr 2020, Gel status: 1

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Gene: itgam 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: ITGAM was added gene: ITGAM was added to Complement deficiencies_MGHA_AGHA_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Immunology Flagship Mode of inheritance for gene: ITGAM was set to Unknown