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Validated All-in-One™ qPCR Primer for MNX1(NM_005515.4) Search again
Product ID:
HQP155003
(click here to view gene annotation page)
Powered by BiozSpecies:
Human
Symbol:
Alias:
HB9, HLXB9, HOXHB9, SCRA1
Gene Description:
motor neuron and pancreas homeobox 1
Target Gene Accession:
NM_005515.4(click here to view gene page)
Estimated Delivery:
Approximately 1-3 weeks, but may vary. Please email sales@genecopoeia.com or call 301-762-0888 to confirm ETA.
Important Note:
By default, qPCR primer pairs are designed to measure the expression level of the splice variant (accession number) you selected for this gene WITHOUT consideration of other possible variants of this gene. If this gene has multiple variants, and you would like to measure the expression levels of one particular variant, multiple variants, or all variants, please contact us for a custom service project at inquiry@genecopoeia.com.
Gene References into function
- mutation in the HLXB9 transcription factor causes an autosomal dominant form of sacral agenesis
- The chromosomal rearrangements of the HLXB9 protein locus at 7q36 were not detected in Hodgkin lymphoma cells unlike acute myeloid leukemia subsets expressing HLXB9.
- High incidence of t(7;12)(q36;p13) in infant myeloid leukemia is associated with ectopic expression of HLXB9.
- This study confirms that familial Currarino syndrome (CS) patients in Korea have the same genetic background as other ethnicities and reaffirms the phenotype variability among CS patients with the same mutation.
- report 23 novel mutations in 26 patients among a series of 50 index cases with Currarino syndrome
- MNX1-ETV6 fusion gene in an acute megakaryoblastic leukemia.