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

Configure this page

Share this page

Bookmark this page

.

Gene: HNF4G ENSBTAG00000008280

.

Description

hepatocyte nuclear factor 4 gamma [Source:VGNC Symbol;Acc:VGNC:29892]

Location

Primary_assembly 14: 38,696,412-38,831,325 forward strand.

ARS-UCD2.0:CM008181.2

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
ENSBTAT00000010892.7	HNF4G-202	3844	462aa	ENSBTAP00000010892.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1MGG2	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,
ENSBTAT00000090945.2	HNF4G-201	3544	408aa	ENSBTAP00000102049.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9TTV4	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,

.

Summary

.

.