Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

Configure this page

Share this page

Bookmark this page

.

Gene: SEPTIN1 ENSPTRG00000007998

.

Description

septin 1 [Source:VGNC Symbol;Acc:VGNC:13768]

Gene Synonyms

SEPT1

Location

Chromosome 16: 29,281,386-29,286,204 reverse strand.

Pan_tro_3.0:CM000330.3

About this gene

This gene has 2 transcripts (splice variants), 105 orthologues and 16 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000014761.6	SEPTIN1-201	1690	414aa	ENSPTRP00000013670.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A6D2VV78 H2QAX3	A single transcript chosen for a gene which is the most conserved, most highly expressed, has the longest coding sequence and is represented in other key resources, such as NCBI and UniProt. This is defined in detail on http://www.ensembl.org/info/genome/genebuild/canonical.htmlEnsembl Canonical, APPRIS P1: Transcript(s) expected to code for the main functional isoform based solely on the core modules in the APPRIS. APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods to identify the most functionally important transcript(s) of a gene. APPRIS P1,
ENSPTRT00000100198.1	SEPTIN1-202	213	70aa	ENSPTRP00000061936.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2I3RBC3 A0A6D2XUM7	-

.

Summary

.

.