Name

MNX1 Gene

motor neuron and pancreas homeobox 1

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]

MNX1-AS1 Gene

MNX1 antisense RNA 1 (head to head)

mnx1 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term mnx1 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

MNX1 Gene Set

From NURSA Protein-Protein Interactions

interacting proteins for MNX1 from the NURSA Protein-Protein Interactions dataset.

MNX1 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for MNX1 from the Pathway Commons Protein-Protein Interactions dataset.

mnx1etv6 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term mnx1etv6 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.