SEPT3

Neuronal-specific septin-3 is a protein that in humans is encoded by the SEPT3 gene.[5]

SEPTIN3
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesSEPTIN3, SEP3, bK250D10.3, septin 3, SEPT3
External IDsOMIM: 608314 MGI: 1345148 HomoloGene: 99740 GeneCards: SEPTIN3
Gene location (Human)
Chr.Chromosome 22 (human)[1]
Band22q13.2Start41,969,475 bp[1]
End41,998,221 bp[1]
Orthologs
SpeciesHumanMouse
Entrez

55964

24050

Ensembl

ENSG00000100167

ENSMUSG00000022456

UniProt

Q9UH03

Q9Z1S5

RefSeq (mRNA)

NM_145734
NM_019106
NM_145733
NM_001363845

RefSeq (protein)

NP_061979
NP_663786
NP_001350774

NP_036019
NP_001345765
NP_001345766

Location (UCSC)Chr 22: 41.97 – 42 MbChr 15: 82.27 – 82.29 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Function

This gene belongs to the septin family of GTPases. Members of this family are required for cytokinesis. Expression is upregulated by retinoic acid in a human teratocarcinoma cell line. The specific function of this gene has not been determined. Alternative splicing of this gene results in multiple transcript variants.[5]

References

  1. GRCh38: Ensembl release 89: ENSG00000100167 - Ensembl, May 2017
  2. GRCm38: Ensembl release 89: ENSMUSG00000022456 - 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. "Entrez Gene: SEPT3 septin 3".

Further reading

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