Entry Detail



General Information

Database ID:SKCM03153
Cancer Type:melanoma
Dataset:GSE38495
CTCs/CTM Isolation Method:immunomagnetic purification



Gene Information

ncRNA Symbol:SEPT9
Full Name:septin 9
Category:mRNA
Synonyms:AF17q25|MSF|MSF1|NAPB|PNUTL4|SINT1|SeptD1
Chromosome:chr17
Strand:+
Coordinate:
Start Site(bp):77280569End Site(bp):77500596
Gene Summary:This gene is a member of the septin family involved in cytokinesis and cell cycle control. This gene is a candidate for the ovarian tumor suppressor gene. Mutations in this gene cause hereditary neuralgic amyotrophy, also known as neuritis with brachial predilection. A chromosomal translocation involving this gene on chromosome 17 and the MLL gene on chromosome 11 results in acute myelomonocytic leukemia. Multiple alternatively spliced transcript variants encoding different isoforms have been described.[provided by RefSeq, Mar 2009]
External Links:
Ensembl ID:ENSG00000184640
HGNC ID:HGNC:7323
Entrez Gene:10801



Expression Profile of SEPT9 Gene

 







Regulatory Relationship

mRNA targets:NA
miRNA targets:NA
Display:N/A