Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
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- Gene gain/loss tree
- Orthologues
- Paralogues
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Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
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- Structural variants
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ID History
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Gene: Esf1 ENSRNOG00000004777

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Description

ESF1 nucleolar pre-rRNA processing protein homolog [Source:RGD Symbol;Acc:1306067]

Gene Synonyms

LOC366203, RGD1306067

Location

Primary_assembly 3: 147,908,405-147,961,485 reverse strand.

GRCr8:CM070393.1

About this gene

This gene has 1 transcript (splice variant) and 252 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000034487.7	Esf1-201	3404	842aa	ENSRNOP00000037915.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6HQL9 Q76MT4	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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