Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Cellular component
- GO: Biological process
- GO: Molecular function
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: MIEN1 ENSPTRG00000009101

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Description

migration and invasion enhancer 1 [Source:VGNC Symbol;Acc:VGNC:9380]

Location

Chromosome 17: 17,898,983-17,900,652 forward strand.

Pan_tro_3.0:CM000331.3

About this gene

This gene has 2 transcripts (splice variants), 198 orthologues and 5 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000087377.1	MIEN1-201	1119	130aa	ENSPTRP00000070223.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2I3S0W9 A0A6D2XY29	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,
ENSPTRT00000016761.4	MIEN1-202	754	115aa	ENSPTRP00000015509.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A6D2X875 H2QCV2	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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