Cyp27a1 gene
WebCYP27A1 - Diagnostic. Diagnostic testing of this gene is recommended to identify a potential genetic basis for a condition. This type of testing can inform prognosis and clinical care for a symptomatic patient or be used to screen unaffected patients (including family members) for increased genetic risk for the condition. WebClinVar archives and aggregates information about relationships among variation and human health.
Cyp27a1 gene
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WebSep 26, 2024 · Orthologous to human CYP27A1 (cytochrome P450 family 27 subfamily A member 1). [provided by Alliance of Genome Resources, Apr 2024] Cyp27a1 cytochrome P450, family 27, subfamily a, polypeptide 1 [ (house mouse)] ... Data indicate that inhibition of CYP27A1 activity or knockdown and deletion of the Cyp27a1 gene induced … WebCerebrotendinous Xanthomatosis (CTX) is a rare and presumably underdiagnosed, autosomal recessive, metabolic storage disorder. CTX is caused by caused by mutations in the CYP27A1 gene, which encodes for a sterol 27-hydroxylase enzyme important in bile acid synthesis. At least 50 pathogenic mutations have been found in the CYP27A1 gene. …
Webcyp27a1.2. Predicted to enable cholesterol 26-hydroxylase activity and vitamin D3 25-hydroxylase activity. Predicted to be involved in calcitriol biosynthetic process from … WebApr 21, 2024 · For CYP27A1 gene, the rs17470271 T allele frequency was significantly lower with leukopenia (P = 0.039), and the rs933994 T allele frequency was significantly decreased with drug resistance (P = 0.047) (Table 2). Table 2 The positive findings of the associations between vitamin D pathway genes polymorphisms and clinical features of …
WebCYP27A1 INFORMATION. Proteini. Full gene name according to HGNC. Cytochrome P450 family 27 subfamily A member 1. Gene namei. Official gene symbol, which is typically a short form of the gene name, according to HGNC. CYP27A1 (CP27, CTX, CYP27) Protein classi. Assigned HPA protein class (es) for the encoded protein (s). WebCYP27A1. PROTEIN SUMMARY SECTION OVERVIEW RNA DATA ANTIBODY DATA. CYP27A1 INFORMATION. Proteini. Full gene name according to HGNC. Cytochrome …
WebNM_000784.4(CYP27A1):c.578G>A (p.Arg193Gln) AND Cholestanol storage disease Clinical significance: Conflicting interpretations of pathogenicity, Uncertain significance(1); Likely benign(1) (Last evaluated: Oct 26, 2024)
Web头颅mri以脑萎缩、对称性锥体束为主的白质病变和小脑齿状核对称性病变为特征性表现。患者固醇-27-羟化酶（cyp27a1）基因存在c.1477-2a>c纯合突变，为全球首例。鹅脱氧胆酸治疗效果较好。该家系中无类似临床表现患者，但发现了c.1477-2a>c突变基因携带者。 fisher model 98hWebMar 1, 2024 · Background Cerebrotendinous xanthomatosis (CTX) is a rare autosomal recessive lipid storage disease caused by a mutation in the CYP27A1 gene. Due to the disruption of bile acid synthesis leading ... fisher model 667WebEnzymatic oxidation of cholesterol. Cytochrome P450 enzymes (CYP) hydroxylate cholesterol at specific positions to produce hydroxycholesterols, OHCh, and facilitate its elimination to prevent its excess (Pikuleva, 2006). These enzymes include the 7-, 24-, and 27-hydroxylases, CYP7A1, CYP46A1, and CYP27A1, respectively. fisher model pcd-5700 a repairWebClinVar archives and aggregates information about relationships among variation and human health. fisher model ds bookshelf speakersWebClinVar archives and aggregates information about relationships among variation and human health. fisher model 75aWebCYP2R1 is cytochrome P450 2R1, an enzyme which is the principal vitamin D 25-hydroxylase. In humans it is encoded by the CYP2R1 gene located on chromosome 11p15.2. It is expressed in the endoplasmic reticulum in liver, where it performs the first step in the activation of vitamin D by catalyzing the formation of 25-hydroxyvitamin D.. Vitamin … fisher model economicsWebGene target information for CYP27A1. Find diseases associated with this biological target and compounds tested against it in bioassay experiments. fisher model no. rs-1015