Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
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Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
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- Structural variants
Gene expression
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External references
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ID History
- Gene history

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Gene: pgl-2 WBGene00003993

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Description

P granule abnormality protein 2 [Source:NCBI gene (formerly Entrezgene);Acc:182022]

Location

Chromosome III: 8,670,543-8,675,435 reverse strand.

WBcel235:BX284603.4

About this gene

This gene has 2 transcripts (splice variants) and 2 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
B0523.3.2	pgl-2-202	2006	532aa	B0523.3.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	P34266	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,
B0523.3.1	pgl-2-201	1716	532aa	B0523.3.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	P34266	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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