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: MEGF11 ENSSSCG00000004939

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Description

multiple EGF like domains 11 [Source:VGNC Symbol;Acc:VGNC:103126]

Location

Primary_assembly 1: 163,894,312-164,275,442 reverse strand.

Sscrofa11.1:CM000812.5

About this gene

This gene has 4 transcripts (splice variants), 198 orthologues and 4 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000062824.3	MEGF11-203	4640	1140aa	ENSSSCP00000040502.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A287A9M9 A0A8D0RHF6	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 P2: Where the APPRIS core modules are unable to choose a clear principal variant (approximately 25% of human protein coding genes), the database chooses two or more of the CDS variants as "candidates" to be 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 P2,
ENSSSCT00000005450.5	MEGF11-204	5300	953aa	ENSSSCP00000005315.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1SJK2	-
ENSSSCT00000064802.3	MEGF11-201	3911	969aa	ENSSSCP00000054747.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A287BEI6 A0A8D2C8Q7	-
ENSSSCT00000027580.4	MEGF11-202	3487	1030aa	ENSSSCP00000019610.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	I3L6F9	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,

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Summary

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