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: Sema4f ENSRNOG00000006784

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Description

ssemaphorin 4F [Source:RGD Symbol;Acc:3658]

Gene Synonyms

Sema W

Location

Primary_assembly 4: 116,969,137-116,995,442 reverse strand.

GRCr8:CM070394.1

About this gene

This gene has 2 transcripts (splice variants), 182 orthologues, 19 paralogues and is associated with 1 phenotype.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000009269.6	Sema4f-201	3977	776aa	ENSRNOP00000009269.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6IAI3 Q9Z143	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,
ENSRNOT00000138671.1	Sema4f-202	4001	745aa	ENSRNOP00000105847.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-

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Summary

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