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
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: Ccnh ENSRNOG00000031656

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Description

cyclin H [Source:RGD Symbol;Acc:69419]

Location

Primary_assembly 2: 17,570,263-17,614,860 forward strand.

GRCr8:CM070392.1

About this gene

This gene has 4 transcripts (splice variants), 215 orthologues, 6 paralogues and is associated with 28 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000155584.1	Ccnh-204	1458	351aa	ENSRNOP00000111122.1	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,
ENSRNOT00000118807.2	Ccnh-202	2186	329aa	ENSRNOP00000084834.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6A2R2	-
ENSRNOT00000133319.1	Ccnh-203	1420	319aa	ENSRNOP00000107330.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSRNOT00000049423.3	Ccnh-201	1401	323aa	ENSRNOP00000039039.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6I4L7 Q9R1A0	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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Strains

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Genomic alignments

Gene tree

Orthologues

Paralogues

Families (Not available)

More views of comparative genomics data, such as multiple alignments and synteny, are available on the Location page for this gene.

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Personal Data