Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Breeds
Ontologies
- GO: Biological process
- GO: Cellular component
- GO: Molecular function
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: ETV7 ENSSSCG00000001561

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Description

ETS variant transcription factor 7 [Source:VGNC Symbol;Acc:VGNC:87816]

Location

Primary_assembly 7: 32,087,430-32,108,187 reverse strand.

Sscrofa11.1:CM000818.5

About this gene

This gene has 4 transcripts (splice variants), 161 orthologues and 27 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000053128.1	ETV7-202	3525	334aa	ENSSSCP00000043874.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A287AJ08 A0A8D0UHD0	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 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,
ENSSSCT00000074174.1	ETV7-204	3608	279aa	ENSSSCP00000061615.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A5G2QU07 A0A8D1QAP2	-
ENSSSCT00000081281.1	ETV7-203	3315	264aa	ENSSSCP00000070196.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8D1N505 A0A8D1YCT3	APPRIS P2: Where the APPRIS core modules are unable to choose a clear principal variant (approximately 25% of human protein coding genes), the database chooses two or more of the CDS variants as "candidates" to be 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 P2,
ENSSSCT00000001740.5	ETV7-201	3177	214aa	ENSSSCP00000001696.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1RY95	-

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Summary

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