SEPTIN9
Sign in to saveAlso known as AF17q25, MSF, MSF1, NAPB, PNUTL4, SINT1, SeptD1, septin 9
Septin-9 is a protein that in humans is encoded by the SEPT9 gene.
Gene data
SEPTIN9- Name
- septin 9
- Type
- protein-coding
- Position
- 77,280,569–77,500,596 (+)
- Aliases
- AF17q25, MSF, MSF1, PNUTL4, SEPT9, SINT1, SeptD1
- Ensembl
- ENSG00000282302
- RefSeq RNA
- NM_001113491.2, NM_001113492.2, NM_001113493.2, NM_001113494.1, NM_001113495.2
- RefSeq protein
- NP_001106963.1, NP_001106964.1, NP_001106965.1, NP_001106966.1, NP_001106967.2
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].
Gene Ontology
Biological process
Molecular function
Pathways
via MyGene.info
Gene · Ensembl
septin 9
- Symbol
- SEPTIN9
- Biotype
- Protein coding
- Organism
- Homo sapiens
- Location
- Chr HSCHR17_3_CTG4:71,462-85,796
- Strand
- Forward (+)
- Assembly
- GRCh38
via Ensembl · EMBL-EBI
Wikidata facts
- Instance of
- gene
Show 7 more facts
- HomoloGene ID
- 90949
- found in taxon
- Homo sapiens
- exact match
- identifiers.org/ncbigene/10801
- chromosome
- human chromosome 17
- genomic start
- 75276651
- genomic end
- 75496678
- cytogenetic location
- 17q25.3
Sources (3)
via Wikidata · CC0
~1 min read
Encyclopedic overview
6 sectionsContents
- Interactions
- Function
- Clinical significance
- See also
- References
- Further reading
Septin-9 is a protein that in humans is encoded by the SEPT9 gene.
== Interactions ==
Excerpted from Wikipedia’s “SEPTIN9” article, available under the CC BY-SA 4.0 licence.