CRLF3

CRLF3
Identifiers
Aliases	CRLF3 , CREME-9, CREME9, CRLM9, CYTOR4, FRWS, p48.2, cytokine receptor like factor 3
External IDs	OMIM: 614853; MGI: 1860086; HomoloGene: 9327; GeneCards: CRLF3; OMA:CRLF3 - orthologs
Gene location (Human) Chr. Chromosome 17 (human) [1] Band 17q11.2 Start 30,769,388 bp [1] End 30,824,692 bp [1]
Gene location (Mouse) Chr. Chromosome 11 (mouse) [2] Band 11 B5|11 47.43 cM Start 79,937,319 bp [2] End 79,971,817 bp [2]
RNA expression pattern Bgee Human Mouse (ortholog) Top expressed in trabecular bone mononuclear cell monocyte bone marrow blood lymph node epithelium of nasopharynx thymus bone marrow cell mucosa of sigmoid colon Top expressed in neural layer of retina granulocyte spleen blood mesenteric lymph nodes thymus tibiofemoral joint fetal liver hematopoietic progenitor cell bone marrow right lung lobe More reference expression data BioGPS n/a
Gene ontology Molecular function protein binding identical protein binding DNA binding Cellular component plasma membrane cytoplasm cytosol nucleus Biological process negative regulation of cell growth positive regulation of transcription, DNA-templated positive regulation of transcription by RNA polymerase II positive regulation of receptor signaling pathway via JAK-STAT G1/S transition of mitotic cell cycle Sources:Amigo / QuickGO
Orthologs Species Human Mouse Entrez 51379 54394 Ensembl ENSG00000176390 ENSMUSG00000017561 UniProt Q8IUI8 Q9Z2L7 RefSeq (mRNA) NM_015986 NM_001277106 NM_018776 RefSeq (protein) NP_057070 NP_001264035 NP_061246 Location (UCSC) Chr 17: 30.77 – 30.82 Mb Chr 11: 79.94 – 79.97 Mb PubMed search [3] [4]
Wikidata
View/Edit Human View/Edit Mouse

Cytokine receptor-like factor 3 is a protein that in humans is encoded by the CRLF3 gene. ^[5]

Function

Although CRLF3 signaling pathways have not yet been fully characterized it is very likely that CRLF3 is a neuroprotective erythropoietin receptor. ^[6]

Origin

Phylogenetic analyses have shown that CRLF3 at first appeared in a common ancestor of Cnidaria and Bilateria and hence emerged with the origin of the nervous system. ^{[7] [8]}

References

1. GRCh38: Ensembl release 89: ENSG00000176390 – Ensembl, May 2017
2. GRCm38: Ensembl release 89: ENSMUSG00000017561 – Ensembl, May 2017
3. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
4. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
5. "Entrez Gene: cytokine receptor-like factor 3".
6. Hahn N, Knorr DY, Liebig J, Wüstefeld L, Peters K, Büscher M, et al. (2017). "The Insect Ortholog of the Human Orphan Cytokine Receptor CRLF3 Is a Neuroprotective Erythropoietin Receptor". Frontiers in Molecular Neuroscience. 10 223. doi: 10.3389/fnmol.2017.00223 . PMC   5509957 . PMID   28769759.
7. Hahn N, Büschgens L, Schwedhelm-Domeyer N, Bank S, Geurten BR, Neugebauer P, et al. (2019). "The Orphan Cytokine Receptor CRLF3 Emerged With the Origin of the Nervous System and Is a Neuroprotective Erythropoietin Receptor in Locusts". Frontiers in Molecular Neuroscience. 12 251. doi: 10.3389/fnmol.2019.00251 . PMC   6797617 . PMID   31680856.
8. Liongue C, Ward AC (July 2007). "Evolution of Class I cytokine receptors". BMC Evolutionary Biology. 7 (1): 120. Bibcode:2007BMCEE...7..120L. doi: 10.1186/1471-2148-7-120 . PMC   1963337 . PMID   17640376.

External links

• Human CRLF3 genome location and CRLF3 gene details page in the UCSC Genome Browser .

Further reading

• Visser R, Koelma N, Vijfhuizen L, van der Wielen MJ, Kant SG, Breuning MH, et al. (February 2009). "RNF135 mutations are not present in patients with Sotos syndrome-like features". American Journal of Medical Genetics. Part A. 149A (4): 806–8. doi:10.1002/ajmg.a.32694. PMID   19291764. S2CID   10349510.
• Gudbjartsson DF, Walters GB, Thorleifsson G, Stefansson H, Halldorsson BV, Zusmanovich P, et al. (May 2008). "Many sequence variants affecting diversity of adult human height". Nature Genetics. 40 (5): 609–15. doi:10.1038/ng.122. PMID   18391951. S2CID   3005450.
• Zhao J, Li M, Bradfield JP, Zhang H, Mentch FD, Wang K, et al. (June 2010). "The role of height-associated loci identified in genome wide association studies in the determination of pediatric stature". BMC Medical Genetics. 11 96. doi: 10.1186/1471-2350-11-96 . PMC   2894790 . PMID   20546612.
• Yang F, Xu YP, Li J, Duan SS, Fu YJ, Zhang Y, et al. (November 2009). "Cloning and characterization of a novel intracellular protein p48.2 that negatively regulates cell cycle progression". The International Journal of Biochemistry & Cell Biology. 41 (11): 2240–50. doi:10.1016/j.biocel.2009.04.022. PMID   19427400.
• Gevaert K, Goethals M, Martens L, Van Damme J, Staes A, Thomas GR, Vandekerckhove J (May 2003). "Exploring proteomes and analyzing protein processing by mass spectrometric identification of sorted N-terminal peptides". Nature Biotechnology. 21 (5): 566–9. doi:10.1038/nbt810. PMID   12665801. S2CID   23783563.
• Johnatty SE, Beesley J, Chen X, Macgregor S, Duffy DL, Spurdle AB, et al. (July 2010). "Evaluation of candidate stromal epithelial cross-talk genes identifies association between risk of serous ovarian cancer and TERT, a cancer susceptibility "hot-spot"". PLOS Genetics. 6 (7): e1001016. doi: 10.1371/journal.pgen.1001016 . PMC   2900295 . PMID   20628624.
• Barbe L, Lundberg E, Oksvold P, Stenius A, Lewin E, Björling E, et al. (March 2008). "Toward a confocal subcellular atlas of the human proteome". Molecular & Cellular Proteomics. 7 (3): 499–508. doi: 10.1074/mcp.M700325-MCP200 . PMID   18029348.
• Douglas J, Cilliers D, Coleman K, Tatton-Brown K, Barker K, Bernhard B, et al. (August 2007). "Mutations in RNF135, a gene within the NF1 microdeletion region, cause phenotypic abnormalities including overgrowth". Nature Genetics. 39 (8): 963–5. doi:10.1038/ng2083. PMID   17632510. S2CID   35797973.