MDS2

gene
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Summary

MDS2 (myelodysplastic syndrome 2 translocation associated, HGNC:29633) is a long non-coding RNA gene on chromosome 1p36.

Located in extracellular space.

Source: NCBI Gene 259283 — RefSeq curated summary.

At a glance

  • Gene type: non-coding (lncRNA) — 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:29633
Approved symbolMDS2
Namemyelodysplastic syndrome 2 translocation associated
Location1p36
Locus typeRNA, long non-coding
StatusApproved
Ensembl geneENSG00000197880
Ensembl biotypelncRNA
OMIM607305
Entrez259283
RNAcentralURS0000D64BA3 — lncRNA, 1029 nt, 1 organism(s)

Gene structure

Transcript identifiers

Ensembl transcripts: 7 — 7 lncRNA

ENST00000374555, ENST00000477916, ENST00000686180, ENST00000686679, ENST00000795854, ENST00000795855, ENST00000795856

RefSeq mRNA: 0 — MANE Select: None

Canonical transcript exons

ENST00000374555 — 7 exons

ExonStartEnd
ENSE000012713372363910923639251
ENSE000014638152362778123627998
ENSE000014638172362733423627537
ENSE000018016082362850723628597
ENSE000035183712364038923640568
ENSE000035243122363968023639795
ENSE000038203402362948123629557

Expression profiles

Bgee: expression breadth ubiquitous, 129 present calls, max score 74.34.

FANTOM5 (CAGE): breadth tissue_specific, TPM avg 0.3726 / max 71.7291, expressed in 72 samples.

FANTOM5 promoters (2 alternative TSS)

Promoter IDTPM avgSamples expressed
13510.255863
13500.116846

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
male germ line stem cell (sensu Vertebrata) in testisCL:0000089 ∩ UBERON:000047374.34silver quality
sural nerveUBERON:001548868.67silver quality
lymph nodeUBERON:000002968.23gold quality
bloodUBERON:000017866.37gold quality
granulocyteCL:000009466.35gold quality
bone marrow cellCL:000209264.01silver quality
epithelium of nasopharynxUBERON:000195163.11gold quality
cortical plateUBERON:000534362.73silver quality
vermiform appendixUBERON:000115462.41gold quality
leukocyteCL:000073861.61gold quality
caecumUBERON:000115361.08gold quality
left lobe of thyroid glandUBERON:000112060.95gold quality
tonsilUBERON:000237260.56gold quality
thyroid glandUBERON:000204660.46gold quality
right lobe of thyroid glandUBERON:000111960.33gold quality
spleenUBERON:000210660.08gold quality
ventricular zoneUBERON:000305359.65gold quality
ganglionic eminenceUBERON:000402358.98silver quality
small intestine Peyer’s patchUBERON:000345456.58gold quality
bone marrowUBERON:000237156.57silver quality
mucosa of transverse colonUBERON:000499156.18gold quality
vena cavaUBERON:000408755.42gold quality
superficial temporal arteryUBERON:000161455.28gold quality
small intestineUBERON:000210854.85gold quality
stromal cell of endometriumCL:000225554.50gold quality
nasal cavity mucosaUBERON:000182654.29gold quality
hindlimb stylopod muscleUBERON:000425254.06silver quality
tendonUBERON:000004354.04gold quality
skin of hipUBERON:000155453.94silver quality
gingival epitheliumUBERON:000194953.70gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3no2.45

Regulation

Is transcription factor: no

Literature-anchored findings (GeneRIF, showing 1)

  • The product of the ETV6-MDS2 fusion transcript in a patient with myelodysplastic syndrome predicts a short ETV6 protein containing the first 54 amino acids of ETV6 plus four novel amino acids, lacking both the PTN and the DNA-binding domains. (PMID:12203785)

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): B-cell chronic lymphocytic leukemia