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

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Gene: hpl-2 WBGene00001996

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Description

Chromobox protein homolog hpl-2 [Source:NCBI gene (formerly Entrezgene);Acc:176506]

Location

Chromosome III: 10,752,195-10,755,530 reverse strand.

WBcel235:BX284603.4

About this gene

This gene has 3 transcripts (splice variants) and 5 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
K01G5.2c.1	hpl-2-202	993	303aa	K01G5.2c.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	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,
K01G5.2b.1	hpl-2-201	1055	301aa	K01G5.2b.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
K01G5.2a.1	hpl-2-203	691	175aa	K01G5.2a.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	G5EDE2	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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