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Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Gene families
Literature
Metazoan Compara
- Genomic alignments
- Gene tree (Metazoa)
- Gene tree (Protostomes)
- Gene tree (Insects)
- Gene gain/loss tree
- Orthologues
- Paralogues
Pan-taxonomic Compara
- Gene Tree
- Orthologues
Ontologies
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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DB built by WormBase

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Gene: npr-2 WBGene00003808

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Description

G_PROTEIN_RECEP_F1_2 domain-containing protein [Source:NCBI gene;Acc:177790]

Location

Chromosome IV: 9,568,828-9,580,121 reverse strand.

WBcel235:BX284604.4

About this gene

This gene has 4 transcripts (splice variants), 438 orthologues and 17 paralogues.

Transcripts

Show transcript tableHide transcript table

Name	Transcript ID	bp	Protein	Translation ID	Biotype	UniProt	RefSeq	Flags
-	T05A1.1a.1	1595	430aa	T05A1.1a.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	G5ED22	-	APPRIS ALT2: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that appear to be conserved in fewer than three tested species. 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 ALT2,
-	T05A1.1b.1	1475	387aa	T05A1.1b.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q22188	-	-
-	T05A1.1b.2	1395	387aa	T05A1.1b.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q22188	-	-
-	T05A1.1c.1	1239	412aa	T05A1.1c.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A061AKJ8	-	APPRIS P2: Where the APPRIS core modules are unable to choose a clear principal variant (approximately 25% of human protein coding genes), the database chooses two or more of the CDS variants as "candidates" to be the principal variant. 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 P2,

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Summary

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