Gene: AMTN ENSG00000187689

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

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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	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,

Gene gain/loss tree

As of the latest update in March 2020 we are not supporting data for species other than human on this GRCh37 site and the view you wish to use is disabled.

You can read more about why we have done this on our blog.

You can still view this page on the following archive resources:

1. The Ensembl 75 archive represents a code and data freeze taken in February 2014.

2. The GRCh37 archive represents a code and data freeze taken in January 2019.

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Recent locations

Gene: AMTN ENSG00000187689

Gene gain/loss tree