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: Biological process
- GO: Cellular component
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

Gene: NOC4L ENSSHAG00000011598

Description

nucleolar complex associated 4 homolog [Source:HGNC Symbol;Acc:HGNC:28461]

Location

mSarHar1.11:LR735554.1

About this gene

This gene has 1 transcript (splice variant) and 198 orthologues.

Transcripts

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSHAT00000013680.2	NOC4L-201	2960	515aa	ENSSHAP00000013568.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	G3WDR3	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