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
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Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

Gene: sos-1 WBGene00004947

Description

Son of sevenless homolog [Source:NCBI gene;Acc:178846]

Location

WBcel235:BX284605.5

About this gene

Transcripts

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
T28F12.3a.1	-	5232	1493aa	T28F12.3a.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q9N5D3	APPRIS P5: Where the APPRIS core modules are unable to choose a clear principal variant and none of the candidate variants are annotated by CCDS, APPRIS selects the longest of the candidate isoforms as 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 P5,
T28F12.3b.1	-	5224	1493aa	T28F12.3b.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A486WXD9	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,

Summary