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: SEMA3C ENSSSCG00000023784

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Description

semaphorin 3C [Source:VGNC Symbol;Acc:VGNC:92695]

Location

Primary_assembly 9: 99,251,715-99,433,224 forward strand.

Sscrofa11.1:CM000820.5

About this gene

This gene has 1 transcript (splice variant), 199 orthologues and 19 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000031885.4	SEMA3C-201	5387	751aa	ENSSSCP00000021357.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A4X1SJN6 I3LBD8	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,

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Summary

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