Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
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- Orthologues
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- GO: Anatomical entity
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Genetic Variation
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Gene: Amn1 ENSRNOG00000036917

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Description

antagonist of mitotic exit network 1 homolog [Source:RGD Symbol;Acc:1308119]

Gene Synonyms

LOC302032, MGC105998, RGD1308119

Location

Primary_assembly 4: 183,886,474-183,913,411 reverse strand.

GRCr8:CM070394.1

About this gene

This gene has 2 transcripts (splice variants) and 138 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000117439.2	Amn1-202	1238	258aa	ENSRNOP00000089244.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6ABJ0 A6IN73 Q5U201	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,
ENSRNOT00000055441.4	Amn1-201	1186	257aa	ENSRNOP00000052308.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8L2QRD5	-

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Summary

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