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: ERCC6 ENSPTRG00000002488

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Description

ERCC excision repair 6, chromatin remodeling factor [Source:VGNC Symbol;Acc:VGNC:51976]

Location

Chromosome 10: 49,793,156-49,874,767 reverse strand.

Pan_tro_3.0:CM000324.3

About this gene

This gene has 3 transcripts (splice variants), 194 orthologues and 32 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000004641.4	ERCC6-201	5453	1491aa	ENSPTRP00000004282.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	H2Q1W1	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,
ENSPTRT00000102516.1	ERCC6-203	5252	1059aa	ENSPTRP00000061619.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2I3RAX8	-
ENSPTRT00000109074.1	ERCC6-202	5198	1491aa	ENSPTRP00000072559.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	H2Q1W1	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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