MESP1 (mesoderm posterior bHLH transcription factor 1)

2017-04-01  

Identity

HGNC
LOCATION
15q26.1
LOCUSID
ALIAS
bHLHc5
FUSION GENES

Other Information

Locus ID:

NCBI: 55897
MIM: 608689
HGNC: 29658
Ensembl: ENSG00000166823

Variants:

dbSNP: 55897
ClinVar: 55897
TCGA: ENSG00000166823
COSMIC: MESP1

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000166823ENST00000300057Q9BRJ9

Expression (GTEx)

0
5
10
15

References

Pubmed IDYearTitleCitations
372710342023MESP1-knockdown inhibits the proliferation and epithelial mesenchymal transition of hepatocellular carcinoma and enhances the tumor-suppressive effect of 5-fluorouracil.0
372710342023MESP1-knockdown inhibits the proliferation and epithelial mesenchymal transition of hepatocellular carcinoma and enhances the tumor-suppressive effect of 5-fluorouracil.0
364139482022Essential role of MESP1-RING1A complex in cardiac differentiation.0
364139482022Essential role of MESP1-RING1A complex in cardiac differentiation.0
303893442019MESP1 knock-down in human iPSC attenuates early vascular progenitor cell differentiation after completed primitive streak specification.7
317616212019Aberrant expression of embryonic mesendoderm factor MESP1 promotes tumorigenesis.4
303893442019MESP1 knock-down in human iPSC attenuates early vascular progenitor cell differentiation after completed primitive streak specification.7
317616212019Aberrant expression of embryonic mesendoderm factor MESP1 promotes tumorigenesis.4
286777472017MESP1 loss‑of‑function mutation contributes to double outlet right ventricle.3
286777472017MESP1 loss‑of‑function mutation contributes to double outlet right ventricle.3
266942032016MESP1 Mutations in Patients with Congenital Heart Defects.14
266942032016MESP1 Mutations in Patients with Congenital Heart Defects.14
251873012015Dual reporter MESP1 mCherry/w-NKX2-5 eGFP/w hESCs enable studying early human cardiac differentiation.34
251873012015Dual reporter MESP1 mCherry/w-NKX2-5 eGFP/w hESCs enable studying early human cardiac differentiation.34
240560642013Mutational analysis of the human MESP1 gene in patients with congenital heart disease reveals a highly variable sequence in exon 1.6

Citation

Dessen P

MESP1 (mesoderm posterior bHLH transcription factor 1)

Atlas Genet Cytogenet Oncol Haematol. 2017-04-01

Online version: http://atlasgeneticsoncology.org/gene/56735/mesp1-(mesoderm-posterior-bhlh-transcription-factor-1)