MNX1

GENE INFORMATION

? »

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 VIEW

? »
 
 
 
MNX1-001
 
MNX1-003
 
MNX1-004
 
MNX1-005
 
MNX1-006
 
MNX1-201
 
 
 
 
 

PROTEIN INFORMATION

? »

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