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: foxh1 ENSDARG00000055630

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Description

forkhead box H1 [Source:NCBI gene (formerly Entrezgene);Acc:57930]

Location

Chromosome 12: 13,722,385-13,730,501 reverse strand.

GRCz11:CM002896.2

About this gene

This gene has 2 transcripts (splice variants), 195 orthologues, 53 paralogues and is associated with 77 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000078021.7	foxh1-201	5338	472aa	ENSDARP00000072485.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1R6J3	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,
ENSDART00000152370.2	foxh1-202	3213	472aa	ENSDARP00000127073.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1R6J3	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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