Dec 25, 2024 · FTH1 (Ferritin Heavy Chain 1) is a Protein Coding gene. Diseases associated with FTH1 include Hemochromatosis, Type 5 and Neurodegeneration With Brain Iron Accumulation 9 . Among its related pathways are Innate Immune System and Vesicle-mediated transport .

Dec 25, 2024 · This gene encodes the light subunit of the ferritin protein. Ferritin is the major intracellular iron storage protein in prokaryotes and eukaryotes. It is composed of 24 subunits of the heavy and light ferritin chains.

Showing 25 of 4,785 results for FTH1 Search Time: 0 ms in Aliases & Descriptions Drugs & Compounds Disorders Text-Mined Disorders Domains Expression in Human Tissues Function Genomics Localization Orthologs Paralogs Pathways Phenotypes Proteins Publications Summaries Transcripts Variants in category Protein Coding RNA Gene Functional Element ...

Dec 25, 2024 · FTMT (Ferritin Mitochondrial) is a Protein Coding gene. Diseases associated with FTMT include Friedreich Ataxia and Sideroblastic Anemia. Among its related pathways are Insulin receptor recycling and Transport of inorganic cations/anions and amino acids/oligopeptides.

Complete information for lnc-FTH1-3 gene (RNA Gene), , including: function, proteins, disorders, pathways, orthologs, and expression. GeneCards - The Human Gene Compendium

Dec 25, 2024 · FTHL17 (Ferritin Heavy Chain Like 17) is a Protein Coding gene. Diseases associated with FTHL17 include Friedreich Ataxia 2 and Gonadal Dysgenesis. Gene Ontology (GO) annotations related to this gene include ferric iron binding. An …

Dec 24, 2024 · Complete information for ATF1 gene (Protein Coding), Activating Transcription Factor 1, including: function, proteins, disorders, pathways, orthologs, and expression. GeneCards - The Human Gene Compendium

Dec 25, 2024 · Bgee gene expression patterns for FTH1P10 gene: Expressed in male germ line stem cell (sensu Vertebrata) in testis, primordial germ cell in gonad, stromal cell of endometrium and 89 other cell types or tissues.

Dec 24, 2024 · ACSL4 (Acyl-CoA Synthetase Long Chain Family Member 4) is a Protein Coding gene. Diseases associated with ACSL4 include Intellectual Developmental Disorder, X-Linked 63 and Non-Syndromic X-Linked Intellectual Disability .

Dec 25, 2024 · TMSB4X (Thymosin Beta 4 X-Linked) is a Protein Coding gene. Diseases associated with TMSB4X include Osteoarthritis and Hematologic Cancer. Among its related pathways are Response to elevated platelet cytosolic Ca2+ and ERK Signaling. Gene Ontology (GO) annotations related to this gene include RNA binding and actin monomer binding.