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

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Gene: Ergic2 ENSRNOG00000001852

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Description

ERGIC and golgi 2 [Source:RGD Symbol;Acc:1310606]

Gene Synonyms

LOC297728, RGD1310606

Location

Primary_assembly 4: 182,822,225-182,854,490 reverse strand.

GRCr8:CM070394.1

About this gene

This gene has 2 transcripts (splice variants), 262 orthologues and 2 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000079291.3	Ergic2-202	3176	377aa	ENSRNOP00000070726.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0G2JYN4 A6IN52	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,
ENSRNOT00000067970.5	Ergic2-201	3116	357aa	ENSRNOP00000061923.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q5XIS4	-

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Summary

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