Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Gene families
Literature
Metazoan Compara
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
Pan-taxonomic Compara
- Gene Tree
- Orthologues
Ontologies
- GO: Molecular function
- GO: Biological process
- GO: Cellular component
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Regulation
External references
Supporting evidence
ID History
- Gene history

Gene: ninaB FBgn0002937

Description

neither inactivation nor afterpotential B

Location

BDGP6.32:AE014297.3

About this gene

This gene has 1 transcript (splice variant) and 161 orthologues.

Transcripts

Name	Transcript ID	bp	Protein	Translation ID	Biotype	UniProt	RefSeq	Flags
ninaB-RA	FBtr0082820	2164	620aa	FBpp0082288	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q9NKW9 Q9VFS2	NM_142050 NM_142050.3 NP_650307 NP_650307.2	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

Summary