Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Strains
  - Gene tree
  - Orthologues
  - Paralogues
Ontologies
- GO: Cellular component
- GO: Molecular function
- GO: Biological process
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: Amtn ENSRNOG00000003776

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Description

amelotin [Source:RGD Symbol;Acc:1592356]

Gene Synonyms

LOC689404

Location

Primary_assembly 14: 19,648,625-19,661,181 reverse strand.

mRatBN7.2:CM026987.1

About this gene

This gene has 2 transcripts (splice variants), 92 orthologues and is associated with 3 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000065778.4	Amtn-201	1001	212aa	ENSRNOP00000058805.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q3HS82-1	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,
ENSRNOT00000118895.1	Amtn-202	606	201aa	ENSRNOP00000094485.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6AL31	-

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Summary

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