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: SH3PXD2B ENSSSCG00000027378

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Description

SH3 and PX domains 2B [Source:VGNC Symbol;Acc:VGNC:92830]

Location

Primary_assembly 16: 51,733,135-51,858,772 forward strand.

Sscrofa11.1:CM000827.5

About this gene

This gene has 3 transcripts (splice variants), 204 orthologues and 3 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000087704.2	SH3PXD2B-203	7617	930aa	ENSSSCP00000066482.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A5G2QR03	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,
ENSSSCT00000024674.3	SH3PXD2B-201	8170	871aa	ENSSSCP00000025985.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	I3LPF8	-
ENSSSCT00000077427.2	SH3PXD2B-202	2900	907aa	ENSSSCP00000070575.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A5G2RH13	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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Breeds

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Genomic alignments

Gene tree

Orthologues

Paralogues

Families (Not available)

More views of comparative genomics data, such as multiple alignments and synteny, are available on the Location page for this gene.

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Personal Data