Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Breeds
  - Gene tree
  - Orthologues
  - Paralogues
Ontologies
- GO: Cellular component
- GO: Biological process
- GO: Molecular function
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: AMN1 ENSSSCG00000034407

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Description

antagonist of mitotic exit network 1 homolog [Source:VGNC Symbol;Acc:VGNC:97883]

Location

Primary_assembly 5: 42,518,655-42,567,687 forward strand.

Sscrofa11.1:CM000816.5

About this gene

This gene has 3 transcripts (splice variants) and 137 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000070498.1	AMN1-201	3884	241aa	ENSSSCP00000064195.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A5G2QIE4 A0A8D1M6N8	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,
ENSSSCT00000073746.1	AMN1-202	3054	240aa	ENSSSCP00000069783.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A4X1VQI1 A0A5G2QY23	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,
ENSSSCT00000054232.2	AMN1-203	2390	235aa	ENSSSCP00000038668.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A287A4G5 A0A4X1VQJ6	-

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Summary

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