Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
Ontologies
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: cenph ENSDARG00000094892

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Description

centromere protein H [Source:ZFIN;Acc:ZDB-GENE-081104-340]

Gene Synonyms

si:dkey-186m8.3

Location

Chromosome 8: 17,167,876-17,173,694 forward strand.

GRCz11:CM002892.2

About this gene

This gene has 2 transcripts (splice variants), 170 orthologues and is associated with 13 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000134665.2	cenph-201	1043	233aa	ENSDARP00000123314.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A8WHV8	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,
ENSDART00000183901.1	cenph-202	735	233aa	ENSDARP00000157069.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A8WHV8	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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