Description
apoptosis-inducing factor, mitochondrion-associated, 1 [Source:HGNC Symbol;Acc:8768]
Location
Chromosome X: 129,263,337-129,299,861 reverse strand.
Transcripts
This gene has 10 transcripts
NameTranscript IDLength (bp)Protein IDLength (aa)BiotypeCCDS
AIFM1-001ENST000002872952260ENSP00000287295613Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.CCDS14618
AIFM1-002ENST000003199082248ENSP00000315122609Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.CCDS14619
AIFM1-003ENST000003464241200ENSP00000316320326Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
AIFM1-004ENST000004604361925ENSP00000431222274Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
AIFM1-201ENST000004402631925ENSP00000405879261Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.CCDS48166
AIFM1-202ENST000005357242105ENSP00000446113237Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
AIFM1-005ENST000004160732248ENSP00000402535324Nonsense mediated decayTranscript is thought to undergo nonsense mediated decay, a process which detects nonsense mutations and prevents the expression of truncated or erroneous proteins. CCDS48167
AIFM1-006ENST000005278922105ENSP0000043595543Nonsense mediated decayTranscript is thought to undergo nonsense mediated decay, a process which detects nonsense mutations and prevents the expression of truncated or erroneous proteins. -
AIFM1-007ENST00000529877723ENSP0000043299889Nonsense mediated decayTranscript is thought to undergo nonsense mediated decay, a process which detects nonsense mutations and prevents the expression of truncated or erroneous proteins. -
AIFM1-008ENST00000533719845No protein product-Retained intronNoncoding transcript containing intronic sequence. -

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.