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MNX1


Official Full Name
motor neuron and pancreas homeobox 1
Organism
Homo sapiens
Gene ID
3110
Background
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]
Synonyms
HB9; HLXB9; SCRA1; HOXHB9

Cat.No. Product Name Price
SHH343252 shRNA set against Human Mnx1 (NM_005515.3) Inquiry
SHH343256 shRNA set against Mouse Mnx1 (NM_019944.2) Inquiry
SHW005432 shRNA set against Chicken MNX1 (NM_204928) Inquiry
SHW007853 shRNA set against Danio rerio MNX1 (NM_001009885) Inquiry
Cat.No. Product Name Price
CDFH011615 Human MNX1 cDNA Clone(NM_001165255.1) Inquiry
MiUTR1H-04592 MNX1 miRNA 3'UTR clone Inquiry
CDCB166907 Chicken MNX1 ORF Clone (NM_204928) Inquiry
CDCB169328 Danio rerio MNX1 ORF Clone (NM_001009885) Inquiry
CDCB193330 Rabbit MNX1 ORF clone (XM_008263893.1) Inquiry
CDCL133311 Human MNX1 ORF clone (NM_005515.3) Inquiry
CDCL133313 Mouse MNX1 ORF clone (NM_001165255.1) Inquiry
CDCR254544 Mouse Mnx1 ORF Clone(NM_019944.2) Inquiry
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