Gene: Megf8 ENSMUSG00000045039

Description

multiple EGF-like-domains 8 [Source:MGI Symbol;Acc:MGI:2446294]

Gene Synonyms

Egfl4, b2b1702Clo, b2b288Clo, m687Ddg

Location

Chromosome 7: 25,016,589-25,065,342 forward strand.

GRCm39:CM001000.3

About this gene

This gene has 2 transcripts (splice variants), 179 orthologues, 26 paralogues and is associated with 70 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	Flags
ENSMUST00000128119.2	Megf8-201	10040	2789aa	ENSMUSP00000122192.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS52148	P60882	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, The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic, 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, TSL 1: A transcript where all splice junctions are supported by at least one non-suspect mRNA. The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users, based on the type and quality of the alignments used to annotate the transcript. TSL:1,
ENSMUST00000153077.2	Megf8-202	5669	No protein	-	An alternatively spliced transcript believed to contain intronic sequence relative to other, coding, transcripts of the same gene.Retained intron		-	TSL 1: A transcript where all splice junctions are supported by at least one non-suspect mRNA. The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users, based on the type and quality of the alignments used to annotate the transcript. TSL:1,

Gene: Megf8 ENSMUSG00000045039

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Gene: Megf8 ENSMUSG00000045039

Summary

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