MIR595

gene
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Also known as hsa-mir-595

Summary

MIR595 (microRNA 595, HGNC:32851) is a microRNA gene on chromosome 7q36.3.

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.

Source: NCBI Gene 693180 — RefSeq curated summary.

At a glance

  • Gene type: non-coding (miRNA) — no protein product; not a drug target. Variant/disease associations are omitted (they would be positional, from an overlapping protein-coding gene).

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:32851
Approved symbolMIR595
NamemicroRNA 595
Location7q36.3
Locus typeRNA, micro
StatusApproved
Aliaseshsa-mir-595
Ensembl geneENSG00000207637
Ensembl biotypemiRNA
Entrez693180
RNAcentralURS000075B3FD — miRNA, 96 nt, 1 organism(s)

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 miRNA

ENST00000384905

RefSeq mRNA: 0 — MANE Select: None

Canonical transcript exons

ENST00000384905 — 1 exons

ExonStartEnd
ENSE00001499912158532718158532813

Expression profiles

Bgee: expression breadth broad, 48 present calls, max score 82.34.

Top tissues by expression

48 total, by Bgee expression score (0-100, higher = more expressed):

TissueAnatomy IDExpression scoreQuality
monocyteCL:000057682.34gold quality
bloodUBERON:000017878.88gold quality
corpus callosumUBERON:000233676.63gold quality
stomachUBERON:000094574.11gold quality
islet of LangerhansUBERON:000000673.33gold quality
kidneyUBERON:000211372.67gold quality
Ammon’s hornUBERON:000195472.08gold quality
left adrenal gland cortexUBERON:003582571.69gold quality
body of pancreasUBERON:000115071.24gold quality
ascending aortaUBERON:000149670.91gold quality
left adrenal glandUBERON:000123470.65gold quality
body of stomachUBERON:000116170.39gold quality
endometriumUBERON:000129570.14gold quality
lower esophagus muscularis layerUBERON:003583370.13gold quality
lungUBERON:000204869.33gold quality
minor salivary glandUBERON:000183068.35gold quality
skin of abdomenUBERON:000141668.17gold quality
skin of legUBERON:000151167.83gold quality
myometriumUBERON:000129667.58gold quality
transverse colonUBERON:000115766.74gold quality
putamenUBERON:000187466.73gold quality
intestineUBERON:000016066.64gold quality
colonUBERON:000115566.37gold quality
body of uterusUBERON:000985365.84gold quality
amygdalaUBERON:000187665.48gold quality
muscle layer of sigmoid colonUBERON:003580565.39gold quality
pituitary glandUBERON:000000765.34gold quality
ectocervixUBERON:001224965.23gold quality
prostate glandUBERON:000236765.11gold quality
small intestine Peyer’s patchUBERON:000345465.06gold quality

Single-cell (SCXA)

Detected in 1 experiment(s), a significant marker in 0.

ExperimentMarker?Max mean expression
E-ANND-3no0.49

Regulation

Is transcription factor: no

Literature-anchored findings (GeneRIF, showing 8)

  • Overexpression of miR-595 in the sera is associated with active forms of inflammatory bowel disease. (PMID:25628040)
  • ULK1 could inhibit p70S6K in starvation-induced autophagy, and further identified that miR-4487 and miR-595 were novel ULK1 target miRNAs (PMID:26183158)
  • miR-595 played a critical role in carcinogenesis by suppression of SOX7. (PMID:27133048)
  • Authors show that miR-595 expression appears significantly downregulated in the majority of primary samples derived from MDS patients with (-7)/(7q-), in association with RPL27A upregulation. (PMID:27374104)
  • miR-595 was downregulated in epithelial ovarian cancer tissues in comparison with noncancerous ovarian tissues (PMID:29077170)
  • miR-595 acts as a phenotypic regulator of methotrexate sensitivity in CEM/C1 cells by targeting SLC19A1. (PMID:29345051)
  • results revealed that the three RNAs-based biomarker network (long non-coding intergenic RNA-[lncRNA RP11-909B2.1], Homo sapiens microRNA-595 [hsa-miRNA-595], and L3MBTL1 mRNA), had high sensitivity and specificity for discriminating CRC from healthy controls and also from benign colorectal neoplasm. (PMID:29737552)
  • miR-595 suppresses cell proliferation and metastasis in hepatocellular carcinoma by inhibiting NF-kappaB signalling pathway. (PMID:32107085)

Cross-species orthologs

0 orthologs

Protein

Non-coding RNA — no protein product; not a drug target.

Function

No curated pathway, Gene-Ontology, or interaction data.

Disease & clinical

No curated disease, variant, or cancer-driver associations.

Drugs & pharmacology

No drug or pharmacology data — not an established drug target.

  • Disease cohort memberships (association, not causation — diseases whose associated-gene cohort lists this gene; a subset are also under Associated diseases): chronic rhinosinusitis