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

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Gene: PLXNA1 ENSSSCG00000024001

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Description

plexin A1 [Source:VGNC Symbol;Acc:VGNC:91579]

Location

Primary_assembly 13: 73,054,443-73,094,623 reverse strand.

Sscrofa11.1:CM000824.5

About this gene

This gene has 2 transcripts (splice variants), 287 orthologues and 8 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000036894.3	PLXNA1-201	8649	1909aa	ENSSSCP00000039514.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A287A6D8 A0A8D0QNK2	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,
ENSSSCT00000031942.4	PLXNA1-202	8640	1906aa	ENSSSCP00000027438.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8D0QB89 I3LTJ1	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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