Gene: MIR6848

Alternate names for this Gene: hsa-mir-6848

Gene Summary: microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop.

Gene is located in Chromosome: 8

Location in Chromosome : 8q24.3

Description of this Gene: microRNA 6848

Type of Gene: ncRNA

Gene: DGAT1

Alternate names for this Gene: ARAT|ARGP1|DGAT|DIAR7

Gene Summary: This gene encodes an multipass transmembrane protein that functions as a key metabolic enzyme. The encoded protein catalyzes the conversion of diacylglycerol and fatty acyl CoA to triacylglycerol. This enzyme can also transfer acyl CoA to retinol. Activity of this protein may be associated with obesity and other metabolic diseases.

Gene is located in Chromosome: 8

Location in Chromosome : 8q24.3

Description of this Gene: diacylglycerol O-acyltransferase 1

Type of Gene: protein-coding

rs55962377 in MIR6848;DGAT1 gene and Body Height PMID 30595370 2019 Leveraging Polygenic Functional Enrichment to Improve GWAS Power.

rs863225093 in MIR6848;DGAT1 gene and DIARRHEA 7, PROTEIN-LOSING ENTEROPATHY TYPE PMID 26883093 2016 Congenital protein losing enteropathy: an inborn error of lipid metabolism due to DGAT1 mutations.

PMID 23114594 2012 DGAT1 mutation is linked to a congenital diarrheal disorder.