Cyp27a1 gene

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August undefined, 2024

WebThe CYP27A1 gene is a member of the cytochrome P450 gene family. Enzymes produced from the cytochrome P450 genes are involved in the formation and breakdown of various molecules and chemicals within cells. The CYP27A1 gene provides instructions … WebGene target information for CYP27A1. Find diseases associated with this biological target and compounds tested against it in bioassay experiments.

NM_000784.4(CYP27A1):c.1514C>T (p.Thr505Met) AND …

WebThe breakdown of free cholesterol inside Kupffer cells (KCs) by the mitochondrial enzyme CYP27A1 produces 27-hydroxycholesterol (27HC). We recently demonstrated that … Webcyp27a1.2. Predicted to enable cholesterol 26-hydroxylase activity and vitamin D3 25-hydroxylase activity. Predicted to be involved in calcitriol biosynthetic process from calciol and cholesterol metabolic process. Predicted to be active in mitochondrion. Human ortholog (s) of this gene implicated in cerebrotendinous xanthomatosis. smallwoods discount

Cerebrotendinous Xanthomatosis (CTX) - EyeWiki

WebDec 4, 2024 · CYP27A1 cytochrome P450 family 27 subfamily A member 1 Gene ID: 1593, updated on 4-Dec-2024 Gene type: protein coding Also known as: CTX; CP27; CYP27 … CYP27A1 is a gene encoding a cytochrome P450 oxidase, and is commonly known as sterol 27-hydroxylase. This enzyme is located in many different tissues where it is found within the mitochondria. It is most prominently involved in the biosynthesis of bile acids. WebMar 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 ... hildebrand wolfmuller

PXR induces CYP27A1 and regulates cholesterol …

CYP27A1 - Wikipedia

WebJul 1, 2024 · BackgroundCerebrotendinous xanthomatosis (CTX) is an autosomal recessive disorder of bile acid synthesis caused by mutations in the CYP27A1 gene. CTX is an underdiagnosed and potentially treatable disease, thus a detailed appreciation of the phenotypic spectrum and genetic characteristics are crucial for early diagnosis and … WebCYP27A1. PROTEIN SUMMARY SECTION OVERVIEW RNA DATA ANTIBODY DATA. CYP27A1 INFORMATION. Proteini. Full gene name according to HGNC. Cytochrome … hildebrand-benesi equationWebCYP27A1 gene was mapped to chromosome 2q35 between markers D2S1371 and D2S424. It consists of nine exons and eight introns and spans 18.6 kb of DNA.The … smallwoods discount code 70% off

"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). " - Cyp27a1 gene

Cyp27a1 gene

ZFIN Gene: cyp27a1.2 - Zebrafish Information Network

WebJan 7, 2009 · CYP27A1 606530 Clinical Synopsis Toggle Dropdown PheneGene Graphics Linear Radial INHERITANCE - Autosomal recessive [SNOMEDCT: 258211005][UMLS: … WebThe disease is caused by variants affecting the gene represented in this entry; Description. ... Gene name Length; C9J1K5: C9J1K5_HUMAN: CYP27A1: 221: F8WD90: F8WD90_HUMAN: CYP27A1: 115: Features. Showing features for sequence conflict. Type. ID Position(s) Description; Sequence conflict:

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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) WebCYP2R1 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 …

WebEnzymatic 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. 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 …

WebDescription: Homo sapiens cytochrome P450 family 27 subfamily A member 1 (CYP27A1), mRNA; nuclear gene for mitochondrial product. (from RefSeq NM_000784) RefSeq Summary (NM_000784): This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many … 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 - 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.

WebNov 26, 2014 · Cerebrotendinous xanthomatosis (CTX) OMIM#213700 is a rare autosomal-recessive lipid storage disease caused by mutations in the CYP27A1 gene; this gene codes for the mitochondrial enzyme sterol 27-hydroxylase, which is involved in bile acid synthesis. The CYP27A1 gene is located on chromosome 2q33-qter and contains … smallwoods discount code november 2020WebThis gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This endoplasmic reticulum membrane protein catalyzes the first reaction in the cholesterol catabolic … hildebrand york paWebJun 1, 2024 · There are over 200 reported cases of human CYP27A1 gene mutations, which have been linked to cerebrotendinous xanthomatosis (CTX), a rare autosomal recessive disorder of bile acid synthesis. 238, 239, 240 CTX patients have abnormally high levels of cholestanol in the blood and accumulate cholestanol and cholesterol in the brain … hildebrand wineryWebMar 21, 2024 · CYP27A1 (Cytochrome P450 Family 27 Subfamily A Member 1) is a Protein Coding gene. Diseases associated with CYP27A1 include Cerebrotendinous Xanthomatosis and Xanthomatosis . Among … smallwoods discount codes 2022Web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。 hildebrand williston parkWebDec 19, 2013 · Using the human CYP27 cDNA in a study of a panel of Chinese hamster/human hybrid cell clones, Cali and Russell (1991) assigned the CYP27A1 gene … hildebrand-russ funeral home - rhinelanderWebJan 17, 2024 · Cerebrotendinous xanthomatosis (CTX, OMIM 213700) is a rare autosomal recessive condition characterized by disruption of bile acid synthesis due to inactivation of the CYP27A1 gene. Biallelic pathogenic variants are responsible for loss of enzymatic sterol-27-hydroxylase activity leading to reduced production of chenodeoxycholic acid … hildebrand10603.matrixcare.com