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: Eno3 ENSRNOG00000004078

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Description

enolase 3 [Source:RGD Symbol;Acc:2555]

Gene Synonyms

BBE, MGC93623, MSE

Location

Primary_assembly 10: 55,866,101-55,874,540 forward strand.

GRCr8:CM070400.1

About this gene

This gene has 5 transcripts (splice variants), 214 orthologues, 5 paralogues and is associated with 6 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000129606.1	Eno3-204	1843	520aa	ENSRNOP00000111382.1	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,
ENSRNOT00000158058.1	Eno3-205	1770	434aa	ENSRNOP00000100597.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6HG88	-
ENSRNOT00000118138.2	Eno3-203	1731	421aa	ENSRNOP00000077069.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZJD5	-
ENSRNOT00000096738.2	Eno3-202	1703	473aa	ENSRNOP00000093682.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6AK25	-
ENSRNOT00000005612.8	Eno3-201	1645	454aa	ENSRNOP00000005612.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	P15429	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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