SEPTIN12
Sign in to saveAlso known as SPGF10, septin 12, SEPT12
Septin 12 is a protein that in humans is encoded by the SEPT12 gene.
In the Vinony graph
Within Vinony's link graph, SEPTIN12 is referenced by 1 other article, and connects out to PubMed, human chromosome 16 and Ensembl genome database project.
It is catalogued under the topic Genes on human chromosome 16.
Its subject is documented across 5 Wikipedia language editions.
Gene data
SEPTIN12- Name
- septin 12
- Type
- protein-coding
- Position
- 4,777,606–4,788,398 (−)
- Aliases
- SEPT12, SPGF10
- Ensembl
- ENSG00000140623
- RefSeq RNA
- NM_001154458.3, NM_144605.5, XM_006720846.3, XM_011522379.4, XM_017022938.2
- RefSeq protein
- NP_001147930.1, NP_653206.2, XP_006720909.1, XP_011520681.1, XP_016878427.1
This gene encodes a guanine-nucleotide binding protein and member of the septin family of cytoskeletal GTPases. Septins play important roles in cytokinesis, exocytosis, embryonic development, and membrane dynamics. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2011].
Gene Ontology
Biological process
Molecular function
Pathways
via MyGene.info
Gene · Ensembl
septin 12
- Symbol
- SEPTIN12
- Biotype
- Protein coding
- Organism
- Homo sapiens
- Location
- 16:4,777,606-4,788,398
- Strand
- Reverse (−)
- Assembly
- GRCh38
via Ensembl · EMBL-EBI
Wikidata facts
- Instance of
- gene
Show 7 more facts
- found in taxon
- Homo sapiens
- exact match
- identifiers.org/ncbigene/124404
- HomoloGene ID
- 69435
- genomic end
- 4788398
- genomic start
- 4777606
- chromosome
- human chromosome 16
- cytogenetic location
- 16p13.3
Sources (3)
via Wikidata · CC0
~1 min read
Encyclopedic overview
4 sectionsContents
- Function
- References
- Further reading
- External links
Septin 12 is a protein that in humans is encoded by the SEPT12 gene.
== Function ==
Excerpted from Wikipedia’s “SEPTIN12” article, available under the CC BY-SA 4.0 licence.