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Gene Protein Transcript Promoter Expression GO/PPI PubMed Cross reference

Gene information for MNX1 (Homo sapiens)
(Information is obtained from NCBI Gene database)
Entrez gene ID3110
Official gene symbolMNX1
Full namemotor neuron and pancreas homeobox 1
Aliases,HB9,HLXB9,HOXHB9,SCRA1,
Gene summaryThis 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]
LocationChromosome: 7   Locus: 7q36
Gene position156803347 - 156797547  Map Viewer
Gene orientationminus
Gene size5801 bp
Gene sequence
OMIM ID142994