Human (GRCh37.p13)
Description

ameloblastin (enamel matrix protein) [Source:HGNC Symbol;Acc:452]

Location

Chromosome 4: 71,457,973-71,473,005 forward strand.

GRCh37:CM000666.1

About this gene

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

Show/hide columns (1 hidden)
  • Transcript ID
  • Name
  • bp
  • Protein
  • Translation ID
  • Biotype
  • CCDS
  • UniProt Match
  • RefSeq
  • Flags
Transcript IDNamebpProteinBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000322937.6AMBN-0012005447aa
 
Protein coding
CCDS3543Q546D7 Q9NP70 NM_016519.5Ensembl CanonicalGENCODE Basic
ENST00000449493.2AMBN-0021512432aa
 
Protein coding
Q9NP70 -GENCODE Basic

Retirement notice

Human only - retirement of this view

As of Ensembl release 93 this view will no longer be available for human, because we feel that the density of known human genetic variation is too great for the display to be informative in its current form.

Other species will not be affected, as they have less variation data.

For more information about the decision and on how to find variation data for a gene, please see our blog post.

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