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-ps5 ENSRNOG00000033100

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Description

ferritin heavy chain 1, pseudogene 5 [Source:RGD Symbol;Acc:1596174]

Gene Synonyms

LOC689130

Location

Primary_assembly 3: 136,914,906-136,915,776 forward strand.

mRatBN7.2:CM026976.1

About this gene

This gene has 1 transcript (splice variant), 305 orthologues and 25 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000044465.5	Fth1-ps5-201	871	182aa	ENSRNOP00000082812.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZU81	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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