MSX1

GENERAL INFORMATION

? »

Gene name

MSX1

Gene description

Msh homeobox 1

Protein class

Disease related genes
Predicted intracellular proteins
Transcription factors

Predicted localization

Intracellular

Number of transcripts

1
SHOW MORE

HUMAN PROTEIN ATLAS INFORMATION

? »

RNA tissue category

HPA:Tissue enhanced (endometrium)
GTEx:Tissue enhanced (cervix, uterine)

Protein evidence

Evidence at protein level

Protein localization

Most normal tissues displayed moderate nuclear positivity. Strong staining was for example observed in the CNS, airway epithelia, endometrial glandular cells, thyroid and adrenal gland.

ANTIBODY RELIABILITY

? »

Data reliability
description

Pending RNA-based expert annotation.

Data reliability

Uncertain based on 1 antibody.
CAB026198
SHOW MORE

RNA AND PROTEIN EXPRESSION SUMMARY

? »
RNA expression (FPKM) Protein expression (score)
Brain
Endocrine tissues
Bone marrow & immune system
Muscle tissues
Lung
Liver & gallbladder
Pancreas
Gastrointestinal tract
Kidney & urinary bladder
Male tissues
Female tissues
Adipose & soft tissue
Skin
Cerebral cortex

Lymph node

Liver

Colon

Kidney

Testis



PROTEIN EXPRESSION OVERVIEW

? »

Organ

Expression



RNA EXPRESSION OVERVIEW

? »
HPA dataset
RNA tissue category:  Tissue enhanced (endometrium)

Organ

Expression

GTEx dataset
RNA tissue category:  Tissue enhanced (cervix, uterine)

Organ

Expression



GENE INFORMATION

? »

Gene name

MSX1 (HGNC Symbol)

Synonyms

HOX7, HYD1, OFC5

Description

Msh homeobox 1 (HGNC Symbol)

Entrez gene summary

This gene encodes a member of the muscle segment homeobox gene family. The encoded protein functions as a transcriptional repressor during embryogenesis through interactions with components of the core transcription complex and other homeoproteins. It may also have roles in limb-pattern formation, craniofacial development, particularly odontogenesis, and tumor growth inhibition. Mutations in this gene, which was once known as homeobox 7, have been associated with nonsyndromic cleft lip with or without cleft palate 5, Witkop syndrome, Wolf-Hirschom syndrome, and autosomoal dominant hypodontia. [provided by RefSeq, Jul 2008]

Chromosome

4

Cytoband

p16.2

Chromosome location (bp)

4859666 - 4863936

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000163132 (version 78.38)

Entrez gene

4487

UniProt

P28360 (UniProt - Evidence at protein level)

neXtProt

NX_P28360

Antibodypedia

MSX1 antibodies


PROTEIN BROWSER

? »
 
 
 
ENST00000382723
 
 
 
 


PROTEIN INFORMATION

? »

Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)

MSX1-001 ENSP00000372170
ENST00000382723
P28360
Show all »
Show » Show » 303 31.5 No 0