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Metal Metabolism Disorders v1.0 STAB1 Gene migrated from ENSG00000010327 to ENSG00000010327 (gene set migration)
Metal Metabolism Disorders v0.37 STAB1 Zornitza Stark Phenotypes for gene: STAB1 were changed from Iron metabolism metabolism, MONDO:0002279, STAB1-related; Hyperferritinaemia without iron overload to Hyperferritinemia, MIM# 620729
Metal Metabolism Disorders v0.36 STAB1 Zornitza Stark reviewed gene: STAB1: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Hyperferritinemia, MIM# 620729; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Metal Metabolism Disorders v0.35 STAB1 Zornitza Stark Marked gene: STAB1 as ready
Metal Metabolism Disorders v0.35 STAB1 Zornitza Stark Gene: stab1 has been classified as Green List (High Evidence).
Metal Metabolism Disorders v0.35 STAB1 Zornitza Stark Phenotypes for gene: STAB1 were changed from Iron metabolism metabolism, MONDO:0002279, STAB1; Hyperferritinaemia without iron overload to Iron metabolism metabolism, MONDO:0002279, STAB1-related; Hyperferritinaemia without iron overload
Metal Metabolism Disorders v0.34 STAB1 Zornitza Stark Phenotypes for gene: STAB1 were changed from Hyperferritinaemia without iron overload to Iron metabolism metabolism, MONDO:0002279, STAB1; Hyperferritinaemia without iron overload
Metal Metabolism Disorders v0.33 STAB1 Zornitza Stark Classified gene: STAB1 as Green List (high evidence)
Metal Metabolism Disorders v0.33 STAB1 Zornitza Stark Gene: stab1 has been classified as Green List (High Evidence).
Metal Metabolism Disorders v0.32 STAB1 Chern Lim gene: STAB1 was added
gene: STAB1 was added to Iron metabolism disorders. Sources: Literature
Mode of inheritance for gene: STAB1 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: STAB1 were set to 37490907; 28052375
Phenotypes for gene: STAB1 were set to Hyperferritinaemia without iron overload
Review for gene: STAB1 was set to GREEN
gene: STAB1 was marked as current diagnostic
Added comment: PMID: 37490907
- Biallelic variants identified in 10 individuals from 7 families with unexplained hyperferritinaemia without iron overload. All of them were in good health and had no dysmorphologies, psycho-motor development abnormalities, hearing or vision disorders, or other pathologies.
- Homozygous/compound heterozygous variants: missense, frameshift, stopgain, inframe del of 3 AAs, one synonymous.
- Samples from three of the patients from two families showed no immunoreactivity with anti-stabilin-1 compared to control liver where high signal was detected in the liver sinusoids (immunohistochemistry analysis).
- Patients’ peripheral monocytes and monocyte-derived macrophages showed very little expression of stabilin-1 on CD14+ monocytes and macrophages compared to control subjects (flow cytometry analysis).
- These families have also been published in PMID: 28052375.
Sources: Literature