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
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External references
Supporting evidence
ID History
- Gene history

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Gene: Y17G9B.8 WBGene00021205

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Description

SGF29 C-terminal domain-containing protein [Source:NCBI gene (formerly Entrezgene);Acc:177246]

Location

Chromosome IV: 4,757,177-4,758,840 reverse strand.

WBcel235:BX284604.4

About this gene

This gene has 2 transcripts (splice variants), 199 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
Y17G9B.8.1	Y17G9B.8-202	1522	236aa	Y17G9B.8.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q9N576	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,
Y17G9B.8.2	Y17G9B.8-201	1314	236aa	Y17G9B.8.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q9N576	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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