Overview

Variant ID 20222
Entrez Gene ID 100422857
Gene MIR4318 (GeneCards)
Location hg19 18:36136163-36136163
hg38 18:38556199-38556199
Disease Asymptomatic
Method HiSeq X Ten
Mutation(HGVS format) NC_000018.9:g.36136163 G>A (Genome Assembly: GRCh37)

Other information

Exon or Intron NA
Position in protein NA
Amino acid changes in protein NA > NA
Position in cDNA NA
Changes in cDNA NA > NA
mRNA accession NA
mRNA length NA
Reference length 78077248

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0
EIGEN score 0.02
CADD Raw score (version 1.3) -0.059884 (Deleterious)
FATHMM raw prediction score 0.13594 (Tolerated)
Deleterious probability by DeFine 0.3379 (Neutral)
Entrez Gene ID 100422857 (NCBI Gene)
Official Gene Symbol MIR4318 (GeneCards)
Number of variants in MIR4318 in this database 19 (view all the variants)
Full name microRNA 4318
Band 18q12.2
Other IDs miRBase: MI0015847
HGNC: HGNC:38333
Ensembl: ENSG00000266530
Other names None
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. [provided by RefSeq, Sep 2009]

Individual #1

Individual ID 29217584.03 (view all the variants in this individual)
Pubmed ID 29217584
Whose mosaic mutation Normal  
Phenotype 1  
Disease Asymptomatic
OMIM ID

Publication #1: 29217584

Pubmed ID 29217584
Title Aging and neurodegeneration are associated with increased mutations in single human neurons.
Journal Science
Publication date 2018.02
Disease Cockayne syndrome Xeroderma Pigmentosum
Number of cases Male cases: 3; Female cases: 6; cases of unknown sex: 15;