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

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Gene: foxc1b ENSDARG00000055398

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Description

forkhead box C1b [Source:NCBI gene (formerly Entrezgene);Acc:79375]

Location

Chromosome 20: 26,702,377-26,704,331 forward strand.

GRCz11:CM002904.2

About this gene

This gene has 1 transcript (splice variant), 15 orthologues, 53 paralogues and is associated with 5 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000077753.4	foxc1b-201	1955	433aa	ENSDARP00000072219.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q9DE24	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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