Description
Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1 [Source:HGNC Symbol;Acc:467]
Location
Chromosome X: 109,437,414-109,683,461 reverse strand.
Transcripts
This gene has 5 transcripts
NameTranscript IDLength (bp)Protein IDLength (aa)BiotypeCCDS
AMMECR1-001ENST000002628445504ENSP00000262844333Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.CCDS14551
AMMECR1-002ENST000003720573380ENSP00000361127210Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.CCDS55476
AMMECR1-005ENST000003720593052ENSP00000361129296Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.CCDS35368
AMMECR1-003ENST00000473662418No protein product-Processed transcriptNoncoding transcript that does not contain an open reading frame (ORF). -
AMMECR1-004ENST00000496695546No protein product-Processed transcriptNoncoding transcript that does not contain an open reading frame (ORF). -

Transcript and Gene level displays

In Archive EnsEMBL we provide displays at two levels:

  • Transcript views which provide information specific to an individual transcript such as the cDNA and CDS sequences and protein domain annotation.
  • Gene views which provide displays for data associated at the gene level such as orthologues, paralogues, regulatory regions and splice variants.

This view is a gene level view. To access the transcript level displays select a Transcript ID in the table above and then navigate to the information you want using the menu at the left hand side of the page. To return to viewing gene level information click on the Gene tab in the menu bar at the top of the page.