Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: FOXQ1 ENSSSCG00000000991

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Description

forkhead box Q1 [Source:VGNC Symbol;Acc:VGNC:88225]

Location

Primary_assembly 7: 664,373-665,563 forward strand.

Sscrofa11.1:CM000818.5

About this gene

This gene has 1 transcript (splice variant), 202 orthologues and 35 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000001081.3	FOXQ1-201	1191	397aa	ENSSSCP00000001059.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A4X1STA9 F1RXP2	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,

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Summary

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