CECR1

In today's world, CECR1 has gained unmatched relevance. Whether due to its impact on society, its influence on popular culture or its relevance in history, CECR1 is a topic that deserves to be analyzed and discussed. From its origins to its impact today, CECR1 has left an indelible mark on humanity. In this article, we will explore in detail all aspects related to CECR1, seeking to understand its importance and meaning in different contexts. Through in-depth analysis and a critical look, we hope to shed light on CECR1 and its implications in today's society.

Protein-coding gene in the species Homo sapiens

ADA2
Available structures PDB Human UniProt search: PDBe RCSB List of PDB id codes 3LGD, 3LGG
Identifiers
Aliases	ADA2, ADGF, IDGFL, PAN, SNEDS, CECR1, cat eye syndrome chromosome region, candidate 1, adenosine deaminase 2, VAIHS
External IDs	OMIM: 607575; HomoloGene: 81852; GeneCards: ADA2; OMA:ADA2 - orthologs
Gene location (Human) Chr. Chromosome 22 (human)[1] Band 22q11.1 Start 17,178,790 bp[1] End 17,258,235 bp[1]
RNA expression pattern Bgee Human Mouse (ortholog) Top expressed in monocyte granulocyte bone marrow cells right uterine tube spleen blood lymph node thymus sperm gallbladder n/a More reference expression data BioGPS More reference expression data
Gene ontology Molecular function deaminase activity zinc ion binding adenosine receptor binding adenosine deaminase activity heparin binding hydrolase activity protein homodimerization activity metal ion binding proteoglycan binding growth factor activity Cellular component extracellular region extracellular space azurophil granule lumen cytosol Biological process multicellular organism development neutrophil degranulation hypoxanthine salvage inosine biosynthetic process adenosine catabolic process regulation of signaling receptor activity signal transduction Sources:Amigo / QuickGO
Orthologs Species Human Mouse Entrez 51816 n/a Ensembl ENSG00000093072 n/a UniProt Q9NZK5 n/a RefSeq (mRNA) NM_001282225 NM_001282226 NM_001282227 NM_001282228 NM_001282229 NM_017424 NM_177405 n/a RefSeq (protein) NP_001269154 NP_001269155 NP_001269156 NP_001269157 NP_001269158 NP_803124 n/a Location (UCSC) Chr 22: 17.18 – 17.26 Mb n/a PubMed search [2] n/a
Wikidata
View/Edit Human

Cat eye syndrome critical region protein 1 is a protein that in humans is encoded by the CECR1 gene.^[3][4]

This gene encodes a member of a subfamily of the adenosine deaminase protein family. The encoded protein may act as a growth factor and have adenosine deaminase activity. It may be responsible for some of the phenotypic features associated with cat eye syndrome. Two transcript variants encoding distinct isoforms have been identified for this gene.^[4]

References

1. ^ ^{a b c} GRCh38: Ensembl release 89: ENSG00000093072 – Ensembl, May 2017
2. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
3. ^ Riazi MA, Brinkman-Mills P, Nguyen T, Pan H, Phan S, Ying F, Roe BA, Tochigi J, Shimizu Y, Minoshima S, Shimizu N, Buchwald M, McDermid HE (May 2000). "The human homolog of insect-derived growth factor, CECR1, is a candidate gene for features of cat eye syndrome". Genomics. 64 (3): 277–85. doi:10.1006/geno.1999.6099. PMID 10756095.
4. ^ ^{a b} Hoppe, W.; Gassmann, J.; Hunsmann, N.; Schramm, H. J.; Sturm, M. (August 1975). "Comments on the paper "Relevance of three-dimensional reconstructions of stain distributions for structural analysis of biomolecules"". Hoppe-Seyler's Zeitschrift für Physiologische Chemie. 356 (8): 1317–1320. doi:10.1515/bchm2.1975.356.2.1317. ISSN 0018-4888. PMID 51816. Archived from the original on 2010-12-05. Retrieved 2017-08-30.

External links

• Human CECR1 genome location and CECR1 gene details page in the UCSC Genome Browser.

Further reading

• Charlab R, Valenzuela JG, Andersen J, Ribeiro JM (2001). "The invertebrate growth factor/CECR1 subfamily of adenosine deaminase proteins". Gene. 267 (1): 13–22. doi:10.1016/S0378-1119(01)00393-6. PMID 11311551.
• Footz TK, Brinkman-Mills P, Banting GS, et al. (2001). "Analysis of the cat eye syndrome critical region in humans and the region of conserved synteny in mice: a search for candidate genes at or near the human chromosome 22 pericentromere". Genome Res. 11 (6): 1053–70. doi:10.1101/gr.154901. PMC 311098. PMID 11381032.
• Strausberg RL, Feingold EA, Grouse LH, et al. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. Bibcode:2002PNAS...9916899M. doi:10.1073/pnas.242603899. PMC 139241. PMID 12477932.
• Ota T, Suzuki Y, Nishikawa T, et al. (2004). "Complete sequencing and characterization of 21,243 full-length human cDNAs". Nat. Genet. 36 (1): 40–5. doi:10.1038/ng1285. PMID 14702039.
• Collins JE, Wright CL, Edwards CA, et al. (2005). "A genome annotation-driven approach to cloning the human ORFeome". Genome Biol. 5 (10): R84. doi:10.1186/gb-2004-5-10-r84. PMC 545604. PMID 15461802.
• Gerhard DS, Wagner L, Feingold EA, et al. (2004). "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)". Genome Res. 14 (10B): 2121–7. doi:10.1101/gr.2596504. PMC 528928. PMID 15489334.
• Zavialov AV, Engström A (2006). "Human ADA2 belongs to a new family of growth factors with adenosine deaminase activity". Biochem. J. 391 (Pt 1): 51–7. doi:10.1042/BJ20050683. PMC 1237138. PMID 15926889.
• Otsuki T, Ota T, Nishikawa T, et al. (2007). "Signal sequence and keyword trap in silico for selection of full-length human cDNAs encoding secretion or membrane proteins from oligo-capped cDNA libraries". DNA Res. 12 (2): 117–26. doi:10.1093/dnares/12.2.117. PMID 16303743.

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