Description
colony stimulating factor 1 receptor [Source:HGNC Symbol;Acc:2433]
Location
Chromosome 5: 149,432,854-149,492,935 reverse strand.
Transcripts
This gene has 10 transcripts
NameTranscript IDLength (bp)Protein IDLength (aa)BiotypeCCDS
CSF1R-001ENST000002863013989ENSP00000286301972Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.CCDS4302
CSF1R-004ENST00000511344655ENSP0000042117449Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
CSF1R-201ENST000003943072145ENSP00000377844501Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
CSF1R-202ENST00000543093921ENSP00000445282306Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
CSF1R-002ENST000005048753697ENSP00000422212671Nonsense mediated decayTranscript is thought to undergo nonsense mediated decay, a process which detects nonsense mutations and prevents the expression of truncated or erroneous proteins. -
CSF1R-007ENST00000515068723ENSP0000042754564Nonsense mediated decayTranscript is thought to undergo nonsense mediated decay, a process which detects nonsense mutations and prevents the expression of truncated or erroneous proteins. -
CSF1R-005ENST00000515239584No protein product-Processed transcriptNoncoding transcript that does not contain an open reading frame (ORF). -
CSF1R-003ENST000005026601388No protein product-Retained intronNoncoding transcript containing intronic sequence. -
CSF1R-006ENST00000513609711No protein product-Retained intronNoncoding transcript containing intronic sequence. -
CSF1R-008ENST00000509861886No 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.