Ensembl ID ENSG00000180096 Gene ID 1731 Accession 2879
Gene Symbol SEPTIN1 Alias LARP;SEP1;DIFF6;SEPT1;PNUTL3 Full Name septin 1
Position 16 : 30378135 - 30382815 Length 4681 bases Strand Minus strand
Status Confidence Main interacting RNAsN.A.RBP type Canonical_RBPs
Summary This gene is a member of the septin family of GTPases. Members of this family are required for cytokinesis and the maintenance of cellular morphology. This gene encodes a protein that can form homo- and heterooligomeric filaments, and may contribute to the formation of neurofibrillary tangles in Alzheimer's disease. Alternatively spliced transcript variants have been found but the full-length nature of these variants has not been determined. [provided by RefSeq, Dec 2012]

ENSG00000180096 Expression In 33 Tumors

Ensembl ID Gene symbol Log2 Foldchange Pvaue Cancer
ENSG00000180096 1.83 5.00e-63 KIRC
ENSG00000180096 -0.9 6.93e-12 COAD
Ensembl ID Gene symbol Cancer types Pubmed ID
ENSG00000180096 skin tumors 23087102
Ensembl ID Gene symbol Disease/phenotype Mutation type Mutated / Total samples Literature
Ensembl ID Gene symbol Cancer P-value Which worse show
ENSG00000180096 MESO 0.0018 low
ENSG00000180096 PAAD 0.00032 low
ENSG00000180096 ACC 0.043 low
ENSG00000180096 LGG 0.0076 high
ENSG00000180096 LUSC 0.022 high
ENSG00000180096 HNSC 0.00066 low
ENSG00000180096 READ 0.036 high
ENSG00000180096 KIRP 0.027 low
ENSG00000180096 PCPG 0.0035 low
ENSG00000180096 BRCA 0.0032 low
ENSG00000180096 COAD 0.033 high
ENSG00000180096 OV 0.0039 low
ENSG00000180096 KIRC 0.0024 high
ENSG00000180096 PRAD 0.017 low
ENSG00000180096 BLCA 0.013 low
ENSG00000180096 LAML 0.0024 high
ENSG00000180096 CESC 7e-04 low
Ensembl ID Gene symbol Cancer CNV type -log10(q-value) G-score average amplitude frequency
ENSG00000180096 UCS Amp 0.620785 0.478697 0.671162 0.357143
ENSG00000180096 UCEC Amp 0.760391 0.104429 0.653159 0.105751