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MNX1 Genemotor 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 GeneMNX1 antisense RNA 1 (head to head) |
mnx1 Gene SetFrom 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 SetFrom NURSA Protein-Protein Interactions interacting proteins for MNX1 from the NURSA Protein-Protein Interactions dataset. |
MNX1 Gene SetFrom Pathway Commons Protein-Protein Interactions interacting proteins for MNX1 from the Pathway Commons Protein-Protein Interactions dataset. |
mnx1etv6 Gene SetFrom 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. |