Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
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: PLXNA1 ENSPTRG00000015341

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Description

plexin A1 [Source:VGNC Symbol;Acc:VGNC:2516]

Location

Chromosome 3: 130,183,501-130,237,341 forward strand.

Pan_tro_3.0:CM000317.3

About this gene

This gene has 2 transcripts (splice variants), 288 orthologues and 8 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000107235.1	PLXNA1-201	9168	1915aa	ENSPTRP00000088978.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	K7DJ20	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,
ENSPTRT00000028652.6	PLXNA1-202	5661	1886aa	ENSPTRP00000026442.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	H2QNA6	-

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Summary

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