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: SH3GL1 ENSPTRG00000010308

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Description

SH3 domain containing GRB2 like 1, endophilin A2 [Source:VGNC Symbol;Acc:VGNC:14754]

Location

Chromosome 19: 4,532,171-4,572,375 reverse strand.

Pan_tro_3.0:CM000333.3

About this gene

This gene has 3 transcripts (splice variants), 279 orthologues and 14 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000018936.3	SH3GL1-201	2542	368aa	ENSPTRP00000017525.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A6D2XAG9 K7D3L5	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,
ENSPTRT00000090207.1	SH3GL1-202	1107	368aa	ENSPTRP00000088235.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2I3TG40	-
ENSPTRT00000103585.1	SH3GL1-203	963	320aa	ENSPTRP00000063440.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2I3RFH3 A0A6D2XVN9	-

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Summary

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