Description
Rho GTPase activating protein 6 [Source:HGNC Symbol;Acc:676]
Location
Chromosome X: 11,136,239-11,683,821 reverse strand.
Transcripts
This gene has 11 transcripts
NameTranscript IDLength (bp)Protein IDLength (aa)BiotypeCCDS
ARHGAP6-001ENST000003374145117ENSP00000338967974Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.CCDS14140
ARHGAP6-003ENST000003807183632ENSP00000370094765Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.CCDS14142
ARHGAP6-004ENST000003030253946ENSP00000302312771Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.CCDS14141
ARHGAP6-005ENST000003807172267ENSP00000370093601Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
ARHGAP6-007ENST000003807363883ENSP00000370112771Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.CCDS14141
ARHGAP6-201ENST000003807322073ENSP00000370108690Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
ARHGAP6-202ENST000004135121795ENSP00000389394467Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
ARHGAP6-203ENST000005348602096ENSP00000438135604Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
ARHGAP6-002ENST000004952425303ENSP00000435767690Nonsense mediated decayTranscript is thought to undergo nonsense mediated decay, a process which detects nonsense mutations and prevents the expression of truncated or erroneous proteins. -
ARHGAP6-006ENST00000491514841No protein product-Processed transcriptNoncoding transcript that does not contain an open reading frame (ORF). -
ARHGAP6-008ENST000004893306300No 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.