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

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Gene: FTH1 ENSBTAG00000011184

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Description

ferritin heavy chain 1 [Source:VGNC Symbol;Acc:VGNC:56265]

Location

Primary_assembly 29: 40,477,533-40,484,508 reverse strand.

ARS-UCD1.3:CM008196.2

About this gene

This gene has 2 transcripts (splice variants), 305 orthologues and 18 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000067393.2	FTH1-202	880	226aa	ENSBTAP00000064784.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1LVU1	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,
ENSBTAT00000014853.6	FTH1-201	924	181aa	ENSBTAP00000014853.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	O46414	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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Breeds

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Genomic alignments

Gene tree

Orthologues

Paralogues

Families (Not available)

More views of comparative genomics data, such as multiple alignments and synteny, are available on the Location page for this gene.

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Personal Data