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

Gene: snx-17 WBGene00008927

Description

PX domain-containing protein; Sorting nexin-17 homolog [Source:NCBI gene;Acc:184624]

Location

WBcel235:BX284606.5

About this gene

Transcripts

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
F17H10.3a.1	-	1816	540aa	F17H10.3a.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q19532	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,
F17H10.3b.1	-	1431	476aa	F17H10.3b.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q0G826	-

Summary