Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Cellular component
- GO: Biological process
- GO: Molecular function
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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Gene: STYXL1 ENSPTRG00000019315

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Description

serine/threonine/tyrosine interacting like 1 [Source:VGNC Symbol;Acc:VGNC:14093]

Location

Chromosome 7: 78,231,131-78,283,204 reverse strand.

Pan_tro_3.0:CM000321.4

About this gene

This gene has 3 transcripts (splice variants), 94 orthologues and 34 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000035741.5	STYXL1-201	1259	313aa	ENSPTRP00000033038.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2J8PX28 A0A6D2XXC9	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,
ENSPTRT00000081518.1	STYXL1-202	968	217aa	ENSPTRP00000070433.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2J8PX32 A0A6D2W7M7	-
ENSPTRT00000089270.1	STYXL1-203	849	283aa	ENSPTRP00000065748.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2I3RM31 A0A6D2WB90	-

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Summary

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