MNX1


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].

NameOMIM IDEnsembl IDHGNC IDPHARMGKB IDMap Location
motor neuron and pancreas homeobox 1MIM:142994Ensembl:ENSG00000130675HGNC:HGNC:4979PA1623960417q36.3

GO terms in MNX1


Term TypeEvidence TypeGO Term IDGO Des.
MFISAGO:0000981RNA polymerase II transcription factor activity, sequence-specific DNA binding
MFISMGO:0000981RNA polymerase II transcription factor activity, sequence-specific DNA binding
MFTASGO:0003700DNA-binding transcription factor activity
MFIEAGO:0043565sequence-specific DNA binding
CCIBAGO:0005634nucleus
CCIDAGO:0005634nucleus
CCIDAGO:0005730nucleolus
CCIDAGO:0005829cytosol
BPIEAGO:0006351transcription, DNA-templated
BPTASGO:0006357regulation of transcription by RNA polymerase II
BPTASGO:0006959humoral immune response
BPTASGO:0009653anatomical structure morphogenesis
BPIBAGO:0021520spinal cord motor neuron cell fate specification
BPIBAGO:0031018endocrine pancreas development
BPIBAGO:0048812neuron projection morphogenesis

Gene expression in normal tissue: MNX1

Gene-model tissue-cancer distribution: Bubble Plot

Gene-drug pathway distribution

Pathways in MNX1


DatabasePathway IDPathway Des.
kegghsa04950Maturity onset diabetes of the young - Homo sapiens (human)

Gene-Drug: Aster Plot


Drug IDDrug NameModel Num.
iGMDRD577BIX012946
iGMDRD414MST-3123
iGMDRD137Indisulam3
iGMDRD945ML2146
iGMDRD289Parthenolide1
iGMDRD427ABT7373

Gene in drug-gene network: Network Plot

Gene-drug targets distribution

Gene Structure: PDB

Models in MNX1

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