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

Configure this page

Share this page

Bookmark this page

.

Gene: PLXNC1 ENSSSCG00000000907

.

Description

plexin C1 [Source:VGNC Symbol;Acc:VGNC:91584]

Location

Primary_assembly 5: 88,900,234-89,055,924 reverse strand.

Sscrofa11.1:CM000816.5

About this gene

This gene has 2 transcripts (splice variants), 248 orthologues and 8 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000000991.5	PLXNC1-201	7313	1570aa	ENSSSCP00000000970.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A4X1SJ00 F1SQN2	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,
ENSSSCT00000085407.2	PLXNC1-202	7274	1557aa	ENSSSCP00000073464.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A4X1SKA7 A0A5G2RLY9	-

.

Summary

.

.