SEPT12

SEPT12
Identifiers
AliasesSEPT12, SPGF10, septin 12
External IDsMGI: 1918339 HomoloGene: 69435 GeneCards: SEPT12
Gene location (Human)
Chr.Chromosome 16 (human)[1]
Band16p13.3Start4,777,669 bp[1]
End4,788,521 bp[1]
Orthologs
SpeciesHumanMouse
Entrez

124404

71089

Ensembl

ENSG00000140623

ENSMUSG00000022542

UniProt

Q8IYM1

n/a

RefSeq (mRNA)

NM_001154458
NM_144605

NM_027669
NM_029374

RefSeq (protein)

NP_001147930
NP_653206

n/a

Location (UCSC)Chr 16: 4.78 – 4.79 MbChr 16: 4.99 – 5 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. 1 2 3 GRCh38: Ensembl release 89: ENSG00000140623 - Ensembl, May 2017
  2. 1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000022542 - Ensembl, May 2017
  3. ↑ "Human PubMed Reference:".
  4. ↑ "Mouse PubMed Reference:".
  5. 1 2 "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.
  • 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. 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.
  • 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. 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.

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


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