MNX1

GENERAL INFORMATION

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Gene name

MNX1

Gene description

Motor neuron and pancreas homeobox 1

Protein class

Cancer-related genes
Disease related genes
Plasma proteins
Predicted intracellular proteins
Transcription factors

Predicted localization

Intracellular

Number of transcripts

6
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HUMAN PROTEIN ATLAS INFORMATION

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RNA tissue category

HPA:Tissue enhanced (colon, duodenum, small intestine)
GTEx:Tissue enhanced (pancreas, small intestine)

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:  Tissue enhanced (colon, duodenum, small intestine)

Organ

Expression

GTEx dataset
RNA tissue category:  Tissue enhanced (pancreas, small intestine)

Organ

Expression



GENE INFORMATION

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Gene name

MNX1 (HGNC Symbol)

Synonyms

HB9, HLXB9, HOXHB9, SCRA1

Description

Motor neuron and pancreas homeobox 1 (HGNC Symbol)

Entrez gene summary

This gene encodes a nuclear protein, which contains a homeobox domain and is a transcription factor. Mutations in this gene result in Currarino syndrome, an autosomic dominant congenital malformation. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2009]

Chromosome

7

Cytoband

q36.3

Chromosome location (bp)

156994051 - 157010651

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000130675 (version 78.38)

Entrez gene

3110

UniProt

P50219 (UniProt - Evidence at protein level)

neXtProt

NX_P50219

Antibodypedia

MNX1 antibodies


PROTEIN BROWSER

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ENST00000252971
 
ENST00000425745
 
ENST00000428439
 
ENST00000469500
 
ENST00000479817
 
ENST00000543409
 
 
 
 


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)

MNX1-001 ENSP00000252971
ENST00000252971
P50219
Show all »
Show » Show » 401 40.6 No 0
MNX1-003 ENSP00000474286
ENST00000479817
Show » 31 3.2 No 0
MNX1-004 ENSP00000401158
ENST00000428439
C9K088
Show all »
Show » Show » 82 9.3 No 0
MNX1-005 ENSP00000416458
ENST00000425745
C9JFT4
Show all »
Show » 29 2.8 No 0
MNX1-006 ENSP00000475129
ENST00000469500
S4R464
Show all »
Show » 36 3.5 No 0
MNX1-201 ENSP00000438552
ENST00000543409
P50219
Show all »
Show » Show » 189 20.6 No 0