Description
Rho GTPase activating protein 4 [Source:HGNC Symbol;Acc:674]
Location
Chromosome X: 153,172,821-153,200,452 reverse strand.
Transcripts
This gene has 25 transcripts
NameTranscript IDLength (bp)Protein IDLength (aa)BiotypeCCDS
ARHGAP4-001ENST000003700283372ENSP00000359045986Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.CCDS55540
ARHGAP4-003ENST000003500603235ENSP00000203786946Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.CCDS14736
ARHGAP4-005ENST00000422918642ENSP00000398019214Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
ARHGAP4-009ENST00000454164747ENSP00000412437249Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
ARHGAP4-010ENST00000442172880ENSP00000408656294Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
ARHGAP4-011ENST000003700163095ENSP00000359033925Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
ARHGAP4-017ENST00000442262625ENSP00000398259177Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
ARHGAP4-019ENST00000422091570ENSP00000413782174Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
ARHGAP4-020ENST00000418750586ENSP00000411712196Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
ARHGAP4-024ENST000003937212721ENSP00000377322768Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
ARHGAP4-201ENST000005372062987ENSP00000444169923Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
ARHGAP4-002ENST000004203832817ENSP00000397533625Nonsense mediated decayTranscript is thought to undergo nonsense mediated decay, a process which detects nonsense mutations and prevents the expression of truncated or erroneous proteins. -
ARHGAP4-014ENST000004041273232ENSP00000385042217Nonsense mediated decayTranscript is thought to undergo nonsense mediated decay, a process which detects nonsense mutations and prevents the expression of truncated or erroneous proteins. -
ARHGAP4-004ENST00000488269960No protein product-Processed transcriptNoncoding transcript that does not contain an open reading frame (ORF). -
ARHGAP4-008ENST00000467421798No protein product-Processed transcriptNoncoding transcript that does not contain an open reading frame (ORF). -
ARHGAP4-015ENST000004610521123No protein product-Processed transcriptNoncoding transcript that does not contain an open reading frame (ORF). -
ARHGAP4-018ENST00000470979593No protein product-Processed transcriptNoncoding transcript that does not contain an open reading frame (ORF). -
ARHGAP4-006ENST00000466928840No protein product-Retained intronNoncoding transcript containing intronic sequence. -
ARHGAP4-007ENST00000461739614No protein product-Retained intronNoncoding transcript containing intronic sequence. -
ARHGAP4-012ENST000004702092889No protein product-Retained intronNoncoding transcript containing intronic sequence. -
ARHGAP4-013ENST000004943022667No protein product-Retained intronNoncoding transcript containing intronic sequence. -
ARHGAP4-016ENST000004943971752No protein product-Retained intronNoncoding transcript containing intronic sequence. -
ARHGAP4-021ENST00000460782496No protein product-Retained intronNoncoding transcript containing intronic sequence. -
ARHGAP4-022ENST000004948131939No protein product-Retained intronNoncoding transcript containing intronic sequence. -
ARHGAP4-023ENST00000463905553No 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.