SEPT12

Protein-coding gene in the species Homo sapiens
SEPTIN12
Identifiers
AliasesSEPTIN12, SPGF10, septin 12, SEPT12
External IDsOMIM: 611562; MGI: 1918339; HomoloGene: 69435; GeneCards: SEPTIN12; OMA:SEPTIN12 - orthologs
Gene location (Human)
Chromosome 16 (human)
Chr.Chromosome 16 (human)[1]
Chromosome 16 (human)
Genomic location for SEPTIN12
Genomic location for SEPTIN12
Band16p13.3Start4,777,606 bp[1]
End4,788,398 bp[1]
Gene location (Mouse)
Chromosome 16 (mouse)
Chr.Chromosome 16 (mouse)[2]
Chromosome 16 (mouse)
Genomic location for SEPTIN12
Genomic location for SEPTIN12
Band16|16 A1Start4,804,722 bp[2]
End4,815,716 bp[2]
RNA expression pattern
Bgee
HumanMouse (ortholog)
Top expressed in
  • left testis

  • right testis

  • testicle

  • cerebellar cortex

  • cerebellar hemisphere

  • right hemisphere of cerebellum

  • primary visual cortex

  • C1 segment

  • medulla oblongata

  • mucosa of transverse colon
Top expressed in
  • seminiferous tubule

  • spermatocyte

  • spermatid

  • blastocyst

  • morula

  • secondary oocyte

  • gastrula

  • zygote

  • primary oocyte

  • mucosa of small intestine
More reference expression data
BioGPS
n/a
Gene ontology
Molecular function
  • nucleotide binding
  • GTP binding
  • protein binding
  • phosphatidylinositol binding
  • protein homodimerization activity
  • GDP binding
  • identical protein binding
  • GTPase activity
  • molecular adaptor activity
Cellular component
  • cytoplasm
  • microtubule cytoskeleton
  • perinuclear region of cytoplasm
  • sperm annulus
  • spindle
  • cell projection
  • midbody
  • cleavage furrow
  • motile cilium
  • cytoskeleton
  • cilium
  • stress fiber
  • septin complex
  • nucleus
  • septin ring
  • septin filament array
Biological process
  • cell cycle
  • cell division
  • sperm motility
  • spermatogenesis
  • cell differentiation
  • flagellated sperm motility
  • mitotic cytokinesis
  • septin ring assembly
  • cilium assembly
  • cytoskeleton-dependent cytokinesis
Sources:Amigo / QuickGO
Orthologs
SpeciesHumanMouse
Entrez

124404

71089

Ensembl

ENSG00000140623

ENSMUSG00000022542

UniProt

Q8IYM1

n/a

RefSeq (mRNA)

NM_001154458
NM_144605

NM_027669
NM_029374
NM_001373945

RefSeq (protein)

NP_001147930
NP_653206

n/a

Location (UCSC)Chr 16: 4.78 – 4.79 MbChr 16: 4.8 – 4.82 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Septin 12 is a protein that in humans is encoded by the SEPT12 gene.[5]

Function

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.[5]

References

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000140623 – Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000022542 – Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ a b "Entrez Gene: Septin 12".

Further reading

  • Kuo PL, Chiang HS, Wang YY, Kuo YC, Chen MF, Yu IS, Teng YN, Lin SW, Lin YH (2013). "SEPT12-microtubule complexes are required for sperm head and tail formation". International Journal of Molecular Sciences. 14 (11): 22102–16. doi:10.3390/ijms141122102. PMC 3856054. PMID 24213608.
  • Hall PA, Jung K, Hillan KJ, Russell SE (July 2005). "Expression profiling the human septin gene family". The Journal of Pathology. 206 (3): 269–78. doi:10.1002/path.1789. PMID 15915442. S2CID 42206750.
  • Kinoshita M (2003). "The septins". Genome Biology. 4 (11): 236. doi:10.1186/gb-2003-4-11-236. PMC 329110. PMID 14611653.
  • Ding X, Yu W, Liu M, Shen S, Chen F, Wan B, Yu L (November 2007). "SEPT12 interacts with SEPT6 and this interaction alters the filament structure of SEPT6 in Hela cells". Journal of Biochemistry and Molecular Biology. 40 (6): 973–8. doi:10.5483/bmbrep.2007.40.6.973. PMID 18047794.
  • Kuo YC, Lin YH, Chen HI, Wang YY, Chiou YW, Lin HH, Pan HA, Wu CM, Su SM, Hsu CC, Kuo PL (April 2012). "SEPT12 mutations cause male infertility with defective sperm annulus". Human Mutation. 33 (4): 710–9. doi:10.1002/humu.22028. PMID 22275165. S2CID 7923473.
  • Miyakawa H, Miyamoto T, Koh E, Tsujimura A, Miyagawa Y, Saijo Y, Namiki M, Sengoku K (2012). "Single-nucleotide polymorphisms in the SEPTIN12 gene may be a genetic risk factor for Japanese patients with Sertoli cell-only syndrome". Journal of Andrology. 33 (3): 483–7. doi:10.2164/jandrol.110.012146. PMID 21636737.
  • Lin YH, Wang YY, Chen HI, Kuo YC, Chiou YW, Lin HH, Wu CM, Hsu CC, Chiang HS, Kuo PL (2012). "SEPTIN12 genetic variants confer susceptibility to teratozoospermia". PLOS ONE. 7 (3): e34011. Bibcode:2012PLoSO...734011L. doi:10.1371/journal.pone.0034011. PMC 3316533. PMID 22479503.
  • Lin YH, Lin YM, Wang YY, Yu IS, Lin YW, Wang YH, Wu CM, Pan HA, Chao SC, Yen PH, Lin SW, Kuo PL (May 2009). "The expression level of septin12 is critical for spermiogenesis". The American Journal of Pathology. 174 (5): 1857–68. doi:10.2353/ajpath.2009.080955. PMC 2671274. PMID 19359518.
  • Miyamoto T, Tsujimura A, Miyagawa Y, Koh E, Namiki M, Horikawa M, Saijo Y, Sengoku K (January 2012). "Single nucleotide polymorphisms in the SEPTIN12 gene may be associated with azoospermia by meiotic arrest in Japanese men". Journal of Assisted Reproduction and Genetics. 29 (1): 47–51. doi:10.1007/s10815-011-9679-5. PMC 3252415. PMID 22116646.
  • Overview of all the structural information available in the PDB for UniProt: Q8IYM1 (Septin-12) at the PDBe-KB.

This article incorporates text from the United States National Library of Medicine, which is in the public domain.


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