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: SEMA3F ENSBTAG00000018307

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Description

semaphorin 3F [Source:VGNC Symbol;Acc:VGNC:34431]

Location

Primary_assembly 22: 50,161,315-50,195,135 reverse strand.

ARS-UCD1.3:CM008189.2

About this gene

This gene has 3 transcripts (splice variants), 271 orthologues and 19 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000024362.7	SEMA3F-201	3579	792aa	ENSBTAP00000024362.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1MGN0	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,
ENSBTAT00000076800.2	SEMA3F-202	3486	761aa	ENSBTAP00000072829.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1MF69	APPRIS ALT2: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that appear to be conserved in fewer than three tested species. 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 ALT2,
ENSBTAT00000095860.1	SEMA3F-203	2558	785aa	ENSBTAP00000102913.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	APPRIS P4: Where the APPRIS core modules are unable to choose a clear principal CDS and there is more than one variant with a distinct (but consecutive) CCDS identifiers, APPRIS selects the longest CCDS isoform as the principal variant. 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 P4,

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Summary

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