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

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Gene: NOP56 ENSPTRG00000013179

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Description

NOP56 ribonucleoprotein [Source:VGNC Symbol;Acc:VGNC:6216]

Location

Chromosome 20: 2,513,806-2,519,581 forward strand.

Pan_tro_3.0:CM000334.4

About this gene

This gene has 1 transcript (splice variant), 202 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000024460.4	NOP56-201	1913	594aa	ENSPTRP00000022562.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A6D2WKQ4 G2HGR6	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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