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

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Gene: fth1a ENSDARG00000015551

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Description

ferritin, heavy polypeptide 1a [Source:ZFIN;Acc:ZDB-GENE-000831-2]

Gene Synonyms

fb06g09, fth1, hm:zeh1145, wu:fb06g09, wu:fq18c10, zeh1145

Location

Chromosome 7: 12,927,944-12,936,708 forward strand.

GRCz11:CM002891.2

About this gene

This gene has 2 transcripts (splice variants), 702 orthologues and 11 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000027329.8	fth1a-201	1091	177aa	ENSDARP00000026092.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q9DDT0	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,
ENSDART00000184664.1	fth1a-202	541	177aa	ENSDARP00000155295.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q9DDT0	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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