Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: cd59a ENSDARG00000090615

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Description

CD59 molecule (CD59 blood group) a [Source:ZFIN;Acc:ZDB-GENE-030131-7871]

Location

Chromosome 7: 38,695,719-38,698,664 reverse strand.

GRCz11:CM002891.2

About this gene

This gene has 2 transcripts (splice variants), 70 orthologues, 1 paralogue and is associated with 9 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000126737.4	cd59a-201	1133	118aa	ENSDARP00000107557.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	E7F2M5	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,
ENSDART00000173900.2	cd59a-202	628	118aa	ENSDARP00000142829.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	E7F2M5	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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