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

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Gene: AMTN ENSG00000187689

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Description

amelotin [Source:HGNC Symbol;Acc:33188]

Gene Synonyms

RSTI689, UNQ689

Location

Chromosome 4: 71,384,257-71,398,459 forward strand.

GRCh37:CM000666.1

About this gene

This gene has 2 transcripts (splice variants) and is associated with 1 phenotype.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq	Flags
ENST00000339336.4	AMTN-001	1037	209aa	ENSP00000341013.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS3542	F1T0L8 Q6UX39	NM_212557.2	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, The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,
ENST00000504451.1	AMTN-002	761	208aa	ENSP00000422452.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS68716	Q6UX39	NM_001286731.1	The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,

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Summary

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