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MESP2 mesoderm posterior 2 homolog (mouse) [Homo sapiens (human)]


RefSeq Accession Definition Sequence Price Select
NM_001039958 Homo sapiens mesoderm posterior 2 homolog (mouse) (MESP2), mRNA. Full Length $468.06
ORF Sequence $346.26


Gene Symbol MESP2
Entrez Gene ID 145873
Full Name mesoderm posterior 2 homolog (mouse)
Synonyms SCDO2, bHLHc6
Gene Type protein-coding
Organism Homo sapiens (human)
Genome

15

15q26.1

Summary This gene encodes a member of the bHLH family of transcription factors and plays a key role in defining the rostrocaudal patterning of somites via interactions with multiple Notch signaling pathways. This gene is expressed in the anterior presomitic mesoderm and is downregulated immediately after the formation of segmented somites. This gene also plays a role in the formation of epithelial somitic mesoderm and cardiac mesoderm. Mutations in the MESP2 gene cause autosomal recessive spondylocostal dystosis 2 (SCD02). [provided by RefSeq].
Disorder

MIM: 605195

Spondylocostal dysostosis, autosomal recessive 2, 608681 (3)

mRNA NM_001039958, 90403597
Protein NP_001035047, 90403598
Product mesoderm posterior protein 2
RefSeq Status REVIEWED
Homo sapiens (human)MESP2NP_001035047.1
Pan troglodytes (chimpanzee)MESP2XP_523152.2
Bos taurus (cattle)MESP2XP_871971.1
Mus musculus (house mouse)Mesp2NP_032615.2
Rattus norvegicus (Norway rat)Mesp2XP_218825.4
Gallus gallus (chicken)MESP2NP_989897.1
Gallus gallus (chicken)MESP2XP_001231219.1
Process
IDNameEvidence
GO:0001756somitogenesisIEA
GO:0006355regulation of transcription, DNA-dependentIEA
GO:0007219Notch signaling pathwayIEA
GO:0007275multicellular organismal developmentIEA
GO:0008078mesodermal cell migrationIEA
GO:0045944positive regulation of transcription from RNA polymerase II promoterIEA
Component
IDNameEvidence
GO:0005634nucleusIEA
Function
IDNameEvidence
GO:0003677DNA bindingIEA
GO:0003700sequence-specific DNA binding transcription factor activityIEA
GeneCards MESP2
UniProt Q0VG99
MIM 605195
Ensembl ENSG00000188095
HGNC 29659

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