Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Molecular function
- GO: Cellular component
- 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: Hnf4g ENSRNOG00000008971

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Description

hepatocyte nuclear factor 4, gamma [Source:RGD Symbol;Acc:1310102]

Gene Synonyms

LOC365744

Location

Primary_assembly 2: 99,792,942-99,943,811 reverse strand.

GRCr8:CM070392.1

About this gene

This gene has 2 transcripts (splice variants), 236 orthologues and 11 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000086760.3	Hnf4g-202	3905	462aa	ENSRNOP00000070293.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0G2JXJ1	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,
ENSRNOT00000011890.8	Hnf4g-201	4117	408aa	ENSRNOP00000011890.7	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1M342	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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