Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Breeds
Ontologies
- GO: Cellular component
- GO: Biological process
- GO: Molecular function
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: NOP56 ENSSSCG00000027676

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Description

NOP56 ribonucleoprotein [Source:VGNC Symbol;Acc:VGNC:95703]

Location

Primary_assembly 17: 32,960,102-32,965,370 reverse strand.

Sscrofa11.1:CM000828.5

About this gene

This gene has 2 transcripts (splice variants), 202 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000007848.5	NOP56-202	1965	596aa	ENSSSCP00000007637.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A4X1SJ12 A0A8D2A0N5	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,
ENSSSCT00000029302.4	NOP56-201	1861	570aa	ENSSSCP00000021283.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	I3LB64	-

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Summary

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