MIR944

gene
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Also known as hsa-mir-944

Summary

MIR944 (microRNA 944, HGNC:33690) is a microRNA gene on chromosome 3q28.

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 100126340 — 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:33690
Approved symbolMIR944
NamemicroRNA 944
Location3q28
Locus typeRNA, micro
StatusApproved
Aliaseshsa-mir-944
Ensembl geneENSG00000216058
Ensembl biotypemiRNA
Entrez100126340
RNAcentralURS0000663F9C — miRNA, 88 nt, 4 organism(s)

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 miRNA

ENST00000401239

RefSeq mRNA: 0 — MANE Select: None

Canonical transcript exons

ENST00000401239 — 1 exons

ExonStartEnd
ENSE00001546583189829922189830009

Expression profiles

Bgee: expression breadth broad, 19 present calls, max score 80.75.

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
intestineUBERON:000016080.75gold quality
muscle of legUBERON:000138376.64gold quality
kidneyUBERON:000211374.48gold quality
gastrocnemiusUBERON:000138874.30gold quality
colonUBERON:000115569.70gold quality
ectocervixUBERON:001224969.40gold quality
stomachUBERON:000094567.55gold quality
subcutaneous adipose tissueUBERON:000219066.57gold quality
skin of abdomenUBERON:000141666.43gold quality
zone of skinUBERON:000001465.56gold quality
bloodUBERON:000017865.11gold quality
vaginaUBERON:000099664.94gold quality
skin of legUBERON:000151164.47gold quality
esophagus mucosaUBERON:000246963.88gold quality
esophagogastric junction muscularis propriaUBERON:003584163.88gold quality
body of stomachUBERON:000116163.16gold quality
thoracic mammary glandUBERON:000520061.90gold quality
spleenUBERON:000210661.02gold quality
right testisUBERON:000453448.84gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3no0.65

Regulation

Is transcription factor: no

Literature-anchored findings (GeneRIF, showing 22)

  • High miR-944 expression is associated with cervical cancer. (PMID:25156441)
  • Expression of miR-944 and miR-3662 was upregulated in patients with lung cancer in comparison with healthy individuals. (PMID:26079400)
  • The findings suggested that miR-944, as an intronic miRNA and a direct target of DeltaNp63, contributes to the function of DeltaNp63 in the induction of epidermal differentiation. (PMID:26202967)
  • our study showed that miR-944 functions as a novel oncogene and regulates the cisplatin resistance in breast cancer (PMID:26298722)
  • Results showed that miR-944 is a novel upstream negative regulator of SIAH1 and PTP4A1 genes and provided evidence for its functional role in migration and invasion of breast cancer cells. (PMID:27377268)
  • miR-944 can be potentially used as a promising biomarker and novel therapeutic target for human endometrial cancer. (PMID:28178620)
  • restoration of MACC1 expression could abrogate the anti-metastatic effects of miR-944 on colorectal cancer (CRC)cells with enhanced cell migration and invasion. MACC1/Met/AKT signaling may be implicated with the function of miR-944 in CRC cells. Altogether, miR-944 potentially act as a prognostic predictor and a drug-target for CRC patients. (PMID:28498456)
  • that pri-miRNA-944 and miRNA-944 may be involved in early squamous-type differentiation of lung tumors (PMID:29496309)
  • miR-944 was significantly downregulated in cancer tissues and cell lines. Upregulating miR-944 inhibited cellular proliferation and invasion in OS cells by directly targeting VEGF. (PMID:30280196)
  • The overexpression of miR-944 caused G1 phase arrest and increased p53 expression in cancer cells. p53 stability was enhanced by miR-944s targeting E3 ligases COP1 and MDM2. Overexpression of COP1 and MDM2 restored cell growth inhibition caused by miR-944. (PMID:30393117)
  • miR-944 is structurally combined with GATA6 and interacts with downstream proteins (CRT and p-AKT) in colorectal cells. (PMID:30873717)
  • The expression levels of miR-944 in cervical cancer tissues were significantly higher compared with normal tissues. Expression levels of miR-944 in cervical cancer cell lines and tissues with human papillomavirus (HPV) infection were significantly higher compared to those without HPV infection. High miR-944 expression group showed shorter overall survival than the low miR-944 expression group in the advanced FIGO stage. (PMID:31060525)
  • Long noncoding RNA SNHG14 accelerates cell proliferation, migration, invasion and suppresses apoptosis in colorectal cancer cells by targeting miR-944/KRAS axis through PI3K/AKT pathway. (PMID:31799655)
  • Circulating microRNA-944 and its target gene EPHA7 as a potential biomarker for colorectal cancer. (PMID:32421395)
  • Synergetic Effects of Intronic Mature miR-944 and DeltaNp63 Isoforms on Tumorigenesis in a Cervical Cancer Cell Line. (PMID:32764455)
  • LncRNA SNHG6 Induces Epithelial-Mesenchymal Transition of Pituitary Adenoma Via Suppressing MiR-944. (PMID:32935999)
  • MiR-944/CISH mediated inflammation via STAT3 is involved in oral cancer malignance by cigarette smoking. (PMID:32961483)
  • Long Noncoding RNA LINC00899/miR-944/ESR1 Axis Regulates Cervical Cancer Cell Proliferation, Migration, and Invasion. (PMID:34161168)
  • Glioma stem cell-derived exosomal miR-944 reduces glioma growth and angiogenesis by inhibiting AKT/ERK signaling. (PMID:34233294)
  • LncRNA LEMD1-AS1 relieves chondrocyte inflammation by targeting miR-944/PGAP1 in osteoarthritis. (PMID:35686740)
  • Investigation of miR-133a, miR-637 and miR-944 genes expression and their relationship with PI3K/AKT signaling in women with breast cancer. (PMID:36656380)
  • CIRC_0003907 MODULATES SEPSIS-INDUCED MYOCARDIAL INJURY VIA ENHANCING MYD88/NLRP3/NF-KappaB AXIS BY SPONGING MIR-944. (PMID:38010112)

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.

No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.