Bos taurus Gene: MNX1
Summary
InnateDB Gene IDBG-638316.2
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol MNX1
Gene Name motor neuron and pancreas homeobox 1
Synonyms
Species Bos taurus
Ensembl Gene ENSBTAG00000030876
Encoded Proteins
motor neuron and pancreas homeobox 1
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary This gene does not have any Entrez summary - the following is the summary from its human ortholog ENSG00000130675:
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]
Gene Information
Type Protein coding
Genomic Location Chromosome 4:119160835-119164828
Strand Reverse strand
Band
Transcripts
ENSBTAT00000006046 ENSBTAP00000006046
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
They are also associated with 1 interaction(s) predicted by orthology.
Predicted by orthology
Total 1 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0003677 DNA binding
Biological Process
GO:0001764 neuron migration
GO:0008045 motor neuron axon guidance
GO:0009791 post-embryonic development
GO:0021520 spinal cord motor neuron cell fate specification
GO:0021675 nerve development
GO:0021904 dorsal/ventral neural tube patterning
GO:0021953 central nervous system neuron differentiation
GO:0030182 neuron differentiation
GO:0031016 pancreas development
GO:0031018 endocrine pancreas development
GO:0048667 cell morphogenesis involved in neuron differentiation
GO:0048812 neuron projection morphogenesis
GO:0060539 diaphragm development
GO:0060541 respiratory system development
Cellular Component
GO:0005634 nucleus
Orthologs
Species
Homo sapiens
Mus musculus
Gene ID
Gene Order
Pathway Predictions based on Human Orthology Data
NETPATH
REACTOME
KEGG
Maturity onset diabetes of the young pathway
Maturity onset diabetes of the young pathway
INOH
PID NCI
Cross-References
SwissProt
TrEMBL
UniProt Splice Variant
Entrez Gene 789765
UniGene
RefSeq XM_002686987 XM_005205984
HUGO HGNC:4979
OMIM
CCDS
HPRD
IMGT
EMBL
GenPept
RNA Seq Atlas 789765