Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
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- Gene gain/loss tree
- Orthologues
- Paralogues
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
- Variant table
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- Structural variants
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Gene: Nop17l FBgn0033224

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Description

Nop17 like

Gene Synonyms

Nop17l

Location

Primary_assembly 2R: 7,800,785-7,806,385 reverse strand.

BDGP6.54:AE013599.5

About this gene

This gene has 3 transcripts (splice variants), 195 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
FBtr0088901	Nop17l-RC	3831	834aa	FBpp0087975	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q0E9G3	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,
FBtr0088900	Nop17l-RA	3525	834aa	FBpp0087974	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q0E9G3	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,
FBtr0088902	Nop17l-RB	3510	834aa	FBpp0087976	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q0E9G3	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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