Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
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: H1f5 ENSRNOG00000060355

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Description

H1.5 linker histone, cluster member [Source:RGD Symbol;Acc:1590638]

Gene Synonyms

H1-5, Hist1h1b, LOC680522

Location

Primary_assembly 17: 47,421,843-47,477,387 forward strand.

GRCr8:CM070407.1

About this gene

This gene has 2 transcripts (splice variants), 74 orthologues and 8 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000151391.1	H1f5-202	1054	222aa	ENSRNOP00000111662.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	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,
ENSRNOT00000091688.3	H1f5-201	1049	222aa	ENSRNOP00000074300.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D3ZBN0	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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