Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
Ontologies
Phenotypes
Genetic Variation
- Variant table
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- Structural variants
Gene expression
Pathway
Molecular interactions
Regulation
External references
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ID History
- Gene history

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Gene: Septin4 FBgn0259923

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Description

Septin 4

Gene Synonyms

Septin4

Location

Primary_assembly X: 16,684,216-16,695,173 reverse strand.

BDGP6.46:AE014298.5

About this gene

This gene has 7 transcripts (splice variants).

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
FBtr0074368	Septin4-RD	2919	427aa	FBpp0074142	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q0KHR7 Q960I4	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,
FBtr0074369	Septin4-RE	2915	427aa	FBpp0074143	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q0KHR7	-
FBtr0074370	Septin4-RC	2896	427aa	FBpp0074144	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q0KHR7	-
FBtr0074366	Septin4-RF	2750	427aa	FBpp0074140	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q0KHR7	-
FBtr0074367	Septin4-RB	2582	427aa	FBpp0074141	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q0KHR7	-
FBtr0074365	Septin4-RA	2444	427aa	FBpp0074139	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q0KHR7	-
FBtr0074371	Septin4-RG	2433	375aa	FBpp0074145	Gene/transcipt that contains an open reading frame (ORF).Protein coding	C8VV45 Q7KUX3 Q95RN2	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,

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Summary

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