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

Configure this page

Share this page

Bookmark this page

.

Gene: H4c8 ENSRNOG00000054017

.

Description

H4 clustered histone 8 [Source:RGD Symbol;Acc:620814]

Gene Synonyms

H1ft, H4c16, H4c2, H4f16, Hist1h4b, Hist1h4m, Hist2h4, Hist4, Hist4h4, LOC291152, LOC295277, LOC364723

Location

Primary_assembly 17: 47,176,062-47,183,497 forward strand.

GRCr8:CM070407.1

About this gene

This gene has 1 transcript (splice variant), 51 orthologues and 23 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000080490.3	H4c8-201	4287	168aa	ENSRNOP00000071163.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	P62804-1	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,

.

Summary

.

.