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

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Gene: Fth1 ENSRNOG00000022619

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Description

ferritin heavy chain 1 [Source:RGD Symbol;Acc:2635]

Gene Synonyms

Fth

Location

Primary_assembly 1: 206,627,103-206,725,424 forward strand.

mRatBN7.2:CM026974.1

About this gene

This gene has 3 transcripts (splice variants), 305 orthologues, 25 paralogues and is associated with 21 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000119519.1	Fth1-203	927	204aa	ENSRNOP00000079245.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZMC0	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,
ENSRNOT00000030919.6	Fth1-201	887	182aa	ENSRNOP00000037803.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q66HI5	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,
ENSRNOT00000094152.1	Fth1-202	506	136aa	ENSRNOP00000087821.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6A564	-

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Summary

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