Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Biological process
- GO: Molecular function
- GO: Cellular component
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: Sema4c ENSRNOG00000016254

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Description

semaphorin 4C [Source:RGD Symbol;Acc:1562837]

Gene Synonyms

LOC301346, RGD1562837

Location

Primary_assembly 9: 46,287,542-46,297,998 reverse strand.

GRCr8:CM070399.1

About this gene

This gene has 2 transcripts (splice variants), 199 orthologues and 19 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000075882.3	Sema4c-202	3652	853aa	ENSRNOP00000068240.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A096MJS2	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,
ENSRNOT00000021956.8	Sema4c-201	4189	834aa	ENSRNOP00000021956.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6INE2 D4A9J3	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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