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

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Gene: pa2g4b ENSDARG00000070657

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Description

proliferation-associated 2G4, b [Source:NCBI gene (formerly Entrezgene);Acc:323462]

Gene Synonyms

fb37h04, pa2g4l, wu:fb37h04, wu:fb99a12, zgc:65848

Location

Chromosome 23: 25,291,891-25,301,475 forward strand.

GRCz11:CM002907.2

About this gene

This gene has 3 transcripts (splice variants), 76 orthologues and 9 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000016248.9	pa2g4b-201	2018	394aa	ENSDARP00000016160.7	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q6PHD8	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,
ENSDART00000131486.2	pa2g4b-202	780	207aa	ENSDARP00000116029.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	3' truncation in transcript evidence prevents annotation of the end of the CDS.CDS 3' incomplete,
ENSDART00000132271.2	pa2g4b-203	732	No protein	-	An alternatively spliced transcript believed to contain intronic sequence relative to other, coding, transcripts of the same gene.Retained intron	-	-

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Summary

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