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
External references
Supporting evidence
ID History
- Gene history

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Gene: Megf9 ENSRNOG00000005932

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Description

multiple EGF-like-domains 9 [Source:RGD Symbol;Acc:1308330]

Gene Synonyms

Egfl5, LOC313270

Location

Primary_assembly 5: 89,008,679-89,120,731 reverse strand.

GRCr8:CM070395.1

About this gene

This gene has 1 transcript (splice variant), 123 orthologues and 26 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000007812.6	Megf9-201	3265	599aa	ENSRNOP00000007812.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6J807 D4A3L3	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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