Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
Ontologies
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
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ID History
- Gene history

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Gene: ECT2 ENSPTRG00000015634

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Description

epithelial cell transforming 2 [Source:VGNC Symbol;Acc:VGNC:1801]

Location

Chromosome 3: 176,510,054-176,584,452 forward strand.

Pan_tro_3.0:CM000317.3

About this gene

This gene has 3 transcripts (splice variants) and 221 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000099065.1	ECT2-203	2944	958aa	ENSPTRP00000077171.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2I3SJU1	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,
ENSPTRT00000083276.1	ECT2-201	4399	883aa	ENSPTRP00000093330.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2I3TVN1 A0A6D2X7G7	APPRIS ALT2: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that appear to be conserved in fewer than three tested species. 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 ALT2,
ENSPTRT00000029146.5	ECT2-202	4169	914aa	ENSPTRP00000026898.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A6D2XW98 H2QNR6	APPRIS P5: Where the APPRIS core modules are unable to choose a clear principal variant and none of the candidate variants are annotated by CCDS, APPRIS selects the longest of the candidate isoforms as the principal variant. 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 P5,

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Summary

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