This Panel is marked as Internal
Congenital anaemias
Gene: SLC11A2
SLC11A2 (solute carrier family 11 member 2)
EnsemblGeneIds (GRCh38): ENSG00000110911
EnsemblGeneIds (GRCh37): ENSG00000110911
OMIM: 600523, Gene2Phenotype
SLC11A2 is in 3 panels
EnsemblGeneIds (GRCh38): ENSG00000110911
EnsemblGeneIds (GRCh37): ENSG00000110911
OMIM: 600523, Gene2Phenotype
SLC11A2 is in 3 panels
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Details
- Mode of Inheritance
- BIALLELIC, autosomal or pseudoautosomal
- Sources
-
- Illumina TruGenome Clinical Sequencing Services
- UKGTN
- Phenotypes
-
- Hypochromic Microcytic Anemia with Iron Overload
- OMIM
- 600523
- Clinvar variants
- Variants in SLC11A2
- Penetrance
- Complete
- Panels with this gene
History Filter Activity
30 Sep 2015, Gel status: 2
Set Mode of Inheritance
Ellen McDonagh (Genomics England Curator)Model of inheritance for gene SLC11A2 was set to BIALLELIC, autosomal or pseudoautosomal
30 Sep 2015, Gel status: 2
Added New Source
Ellen McDonagh (Genomics England Curator)SLC11A2 was added to Congenital anaemiaspanel. Source: Illumina TruGenome Clinical Sequencing Services
30 Sep 2015, Gel status: 2
Set Mode of Inheritance
Ellen McDonagh (Genomics England Curator)Model of inheritance for gene SLC11A2 was set to BIALLELIC, autosomal or pseudoautosomal
30 Sep 2015, Gel status: 2
Added New Source
Ellen McDonagh (Genomics England Curator)SLC11A2 was added to Congenital anaemiaspanel. Source: UKGTN
28 Apr 2015, Gel status: 2
Added New Source
GEL ()SLC11A2 was added to Congenital anaemiaspanel. Sources: Illumina TruGenome Clinical Sequencing Services
28 Apr 2015, Gel status: 1
Added New Source
GEL ()SLC11A2 was added to Congenital anaemiaspanel. Sources: UKGTN