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
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: asp FBgn0000140

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Description

abnormal spindle

Gene Synonyms

asp

Location

Primary_assembly 3R: 24,753,849-24,760,513 forward strand.

BDGP6.46:AE014297.3

About this gene

This gene has 1 transcript (splice variant), 198 orthologues and 3 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
FBtr0084692	asp-RA	6338	1954aa	FBpp0084071	Gene/transcipt that contains an open reading frame (ORF).Protein coding	B6UW25 B6UW30 B6UW43 B6UW46 B6UW48 B6UW49 B6UW50 B6UW51 B6UW52 B6UW54 B8A3X9 H0RNM3 Q9VC45	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,

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Summary

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