Mar 30, 2025 · FAH (Fumarylacetoacetate Hydrolase) is a Protein Coding gene. Diseases associated with FAH include Tyrosinemia, Type I and Tyrosinemia . Among its related pathways are tyrosine degradation and Metabolism .

Mar 30, 2025 · FAHD1 (Fumarylacetoacetate Hydrolase Domain Containing 1) is a Protein Coding gene. Diseases associated with FAHD1 include Spermatogenic Failure 22 and Premature Ovarian Failure 23. Among its related pathways are Regulation of pyruvate metabolism and Respiratory electron transport.

Mar 30, 2025 · FAAH (Fatty Acid Amide Hydrolase) is a Protein Coding gene. Diseases associated with FAAH include Polysubstance Abuse and Tobacco Addiction. Among its related pathways are Metabolism and Fatty acid metabolism.

Mar 30, 2025 · FANCA (FA Complementation Group A) is a Protein Coding gene. Diseases associated with FANCA include Fanconi Anemia, Complementation Group A and Pituitary Stalk Interruption Syndrome. Among its related pathways are Antiviral mechanism by IFN-stimulated genes and Homologous DNA Pairing and Strand Exchange.

Dec 25, 2024 · Complete information for lnc-FAH-2 gene (RNA Gene), , including: function, proteins, disorders, pathways, orthologs, and expression. GeneCards - The Human Gene Compendium

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Dec 25, 2024 · Complete information for LOC112272621 gene (Functional Element), H3K27ac-H3K4me1 HESC Enhancers GRCh37_chr15:80452567-80453210 And GRCh37_chr15:80453211-80453853, including: function, proteins, disorders, pathways, orthologs, and expression. GeneCards - The Human Gene Compendium

Showing 25 of 4,467 results for FAH 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 ...

Mar 30, 2025 · CELF6 (CUGBP Elav-Like Family Member 6) is a Protein Coding gene. Diseases associated with CELF6 include Autism Spectrum Disorder. Gene Ontology (GO) annotations related to this gene include nucleic acid binding and nucleotide binding. An important paralog of this gene is CELF4.

Mar 30, 2025 · TYR (Tyrosinase) is a Protein Coding gene. Diseases associated with TYR include Albinism, Oculocutaneous, Type Ia and Albinism, Oculocutaneous, Type Ib. Among its related pathways are (S)-reticuline biosynthesis II and MITF-M-dependent gene expression.