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
External references
Supporting evidence
ID History
- Gene history

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Gene: Hfe ENSRNOG00000016967

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Description

homeostatic iron regulator [Source:RGD Symbol;Acc:2793]

Location

Primary_assembly 17: 41,841,252-41,851,208 forward strand.

GRCr8:CM070407.1

About this gene

This gene has 4 transcripts (splice variants), 143 orthologues, 50 paralogues and is associated with 66 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000166102.1	Hfe-204	3544	360aa	ENSRNOP00000104711.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6KLM7	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 ALT2: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that appear to be conserved in fewer than three tested species. 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 ALT2,
ENSRNOT00000130289.1	Hfe-203	3756	332aa	ENSRNOP00000101543.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	APPRIS P2: Where the APPRIS core modules are unable to choose a clear principal variant (approximately 25% of human protein coding genes), the database chooses two or more of the CDS variants as "candidates" to be the principal variant. 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 P2,
ENSRNOT00000022881.8	Hfe-202	2861	272aa	ENSRNOP00000022881.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8L2QCW6 F7EZL1	-
ENSRNOT00000022809.8	Hfe-201	1106	172aa	ENSRNOP00000022809.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6KLM8 O35799 Q9R104	-

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Summary

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