Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
Ontologies
- GO: Molecular function
- GO: Biological process
- GO: Cellular component
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: cenpx ENSDARG00000089291

.

Description

centromere protein X [Source:ZFIN;Acc:ZDB-GENE-110411-78]

Gene Synonyms

si:ch73-362i18.3, stra13

Location

Chromosome 3: 57,825,938-57,830,023 forward strand.

GRCz11:CM002887.2

About this gene

This gene has 2 transcripts (splice variants) and 139 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000128815.4	cenpx-201	495	81aa	ENSDARP00000109030.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	E7F1X6	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,
ENSDART00000148693.2	cenpx-202	468	49aa	ENSDARP00000124475.1	Nonsense mediated decay	F8W373	-

.

Summary

.

.