Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Breeds
  - Gene tree
  - Orthologues
  - Paralogues
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: SH3YL1 ENSBTAG00000020495

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Description

SH3 and SYLF domain containing 1 [Source:VGNC Symbol;Acc:VGNC:34584]

Location

Primary_assembly 8: 112,763,456-112,825,612 forward strand.

ARS-UCD2.0:CM008175.2

About this gene

This gene has 6 transcripts (splice variants) and 200 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000110843.1	SH3YL1-206	1849	398aa	ENSBTAP00000089751.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9T039	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,
ENSBTAT00000093132.1	SH3YL1-203	2116	345aa	ENSBTAP00000089718.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9SWL9	-
ENSBTAT00000097540.2	SH3YL1-204	2034	349aa	ENSBTAP00000076556.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9RTY3	-
ENSBTAT00000124474.2	SH3YL1-201	1893	375aa	ENSBTAP00000076815.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9RZN9	-
ENSBTAT00000030504.6	SH3YL1-202	1718	337aa	ENSBTAP00000030484.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAF6ZAT2	-
ENSBTAT00000134512.2	SH3YL1-205	1279	322aa	ENSBTAP00000080276.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9S2X9	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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