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

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Gene: ind FBgn0025776

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Description

intermediate neuroblasts defective

Gene Synonyms

ind

Location

Primary_assembly 3L: 15,042,799-15,043,924 reverse strand.

BDGP6.54:AE014296.5

About this gene

This gene has 1 transcript (splice variant), 3 orthologues and 12 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
FBtr0333875	ind-RB	1126	320aa	FBpp0306007	Gene/transcipt that contains an open reading frame (ORF).Protein coding	O96620 Q6IL70 Q7KUL4 Q963L0	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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