Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: SH3PXD2A ENSDARG00000060148

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Description

SH3 and PX domains 2Aa [Source:ZFIN;Acc:ZDB-GENE-060503-271]

Location

Chromosome 1: 47,585,700-47,686,888 forward strand.

GRCz11:CM002885.2

About this gene

This gene has 2 transcripts (splice variants), 200 orthologues, 5 paralogues and is associated with 10 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000153746.3	SH3PXD2A-201	6887	1085aa	ENSDARP00000127586.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	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, 5' truncation in transcript evidence prevents annotation of the start of the CDS.CDS 5' incomplete,
ENSDART00000084457.5	SH3PXD2A-202	3207	1068aa	ENSDARP00000078892.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	T1ECT1	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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