MESP2

GENERAL INFORMATION

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Gene name

MESP2

Gene description

Mesoderm posterior basic helix-loop-helix transcription factor 2

Protein class

Disease related genes
Predicted intracellular proteins
Transcription factors

Predicted localization

Intracellular

Number of transcripts

2
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HUMAN PROTEIN ATLAS INFORMATION

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RNA tissue category

HPA:Not detected
GTEx:Mixed

Protein evidence

Evidence at protein level

ANTIBODY RELIABILITY

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Data reliability

Pending normal tissue annotation.
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RNA AND PROTEIN EXPRESSION SUMMARY

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RNA expression (FPKM) Protein expression (score)
Brain
N/A
Endocrine tissues
N/A
Bone marrow & immune system
N/A
Muscle tissues
N/A
Lung
N/A
Nasopharynx
N/A
N/A
Bronchus
N/A
N/A
Lung
N/A
Liver & gallbladder
N/A
Liver
N/A
Pancreas
N/A
Pancreas
N/A
Gastrointestinal tract
N/A
Kidney & urinary bladder
N/A
Male tissues
N/A
Testis
N/A
Epididymis
N/A
N/A
Prostate
N/A
Seminal vesicle
N/A
N/A
Female tissues
N/A
Breast
N/A
N/A
Vagina
N/A
N/A
Cervix, uterine
N/A
N/A
Ovary
N/A
Placenta
N/A
Adipose & soft tissue
N/A
Skin
N/A
Skin
N/A


PROTEIN EXPRESSION OVERVIEW

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Pending normal tissue annotation.


RNA EXPRESSION OVERVIEW

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HPA dataset
RNA tissue category:  Not detected

Organ

Expression

GTEx dataset
RNA tissue category:  Mixed

Organ

Expression



GENE INFORMATION

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Gene name

MESP2 (HGNC Symbol)

Synonyms

bHLHc6, SCDO2

Description

Mesoderm posterior basic helix-loop-helix transcription factor 2 (HGNC Symbol)

Entrez gene 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, Oct 2008]

Chromosome

15

Cytoband

q26.1

Chromosome location (bp)

89760591 - 89778754

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000188095 (version 78.38)

Entrez gene

145873

UniProt

Q0VG99 (UniProt - Evidence at protein level)

neXtProt

NX_Q0VG99

Antibodypedia

MESP2 antibodies


PROTEIN BROWSER

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ENST00000341735
 
ENST00000560219
 
 
 
 


PROTEIN INFORMATION

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Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)

MESP2-001 ENSP00000342392
ENST00000341735
Q0VG99
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Show » Show » 397 41.8 No 0
MESP2-002 ENSP00000452998
ENST00000560219
H0YKZ5
Show all »
Show » 99 10.6 No 0