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

Gene: NOL11 ENSOPRG00000008767

Description

nucleolar protein 11 [Source:HGNC Symbol;Acc:HGNC:24557]

Location

About this gene

This gene has 1 transcript (splice variant) and 211 orthologues.

Transcripts

Transcript ID	Name	bp	Protein	Translation ID	Biotype	Flags
ENSOPRT00000008777.1	NOL11-201	2157	718aa	ENSOPRP00000008032.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	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,

Summary