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
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: Gnl1 ENSRNOG00000000798

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Description

G protein nucleolar 1 [Source:RGD Symbol;Acc:1303051]

Location

Primary_assembly 20: 2,787,940-2,797,577 reverse strand.

GRCr8:CM070410.1

About this gene

This gene has 3 transcripts (splice variants), 194 orthologues, 6 paralogues and is associated with 1 phenotype.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000120770.2	Gnl1-203	2155	617aa	ENSRNOP00000106505.1	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,
ENSRNOT00000120545.2	Gnl1-202	2053	607aa	ENSRNOP00000098187.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6KT59 Q6MG06	-
ENSRNOT00000090999.4	Gnl1-201	1858	542aa	ENSRNOP00000073902.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0G2K6Q5	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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Paralogues

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