Carboxypeptidase x, m14 family member 2

CPXM2
Identifiers
Aliases	CPXM2, CPX2, UNQ676, carboxypeptidase X (M14 family), member 2, carboxypeptidase X, M14 family member 2
External IDs	OMIM: 617348; MGI: 1926006; HomoloGene: 69259; GeneCards: CPXM2; OMA:CPXM2 - orthologs
Gene location (Human)
Chr.	Chromosome 10 (human)
End	123,940,267 bp
Gene location (Mouse)
Chr.	Chromosome 7 (mouse)
End	131,756,468 bp
RNA expression pattern
	Top expressed in
	right coronary artery; ; ascending aorta; ; Descending thoracic aorta; ; saphenous vein; ; vena cava; ; pericardium; ; trigeminal ganglion; ; left coronary artery; ; urethra; ; trachea;
	Top expressed in
	vestibular sensory epithelium; ; corneal stroma; ; retinal pigment epithelium; ; interventricular septum; ; utricle; ; myocardium of ventricle; ; esophagus; ; calvaria; ; iris; ; stria vascularis;
	More reference expression data
	n/a
Gene ontology
Molecular function	zinc ion binding; metallocarboxypeptidase activity; serine-type carboxypeptidase activity;
Cellular component	extracellular region; extracellular space;
Biological process	protein processing; peptide metabolic process; proteolysis;
	Sources:Amigo / QuickGO
Orthologs
	119587
	55987
	ENSG00000121898
	ENSMUSG00000030862
	Q8N436
	Q9D2L5
	NM_198148
	NM_018867
	NP_937791
	NP_061355
	Wikidata
View/Edit Human	View/Edit Mouse

Carboxypeptidase X, M14 family member 2 is a protein that in humans is encoded by the CPXM2 gene. ^[5]

References

^ ^a ^b ^c GRCh38: Ensembl release 89: ENSG00000121898 – Ensembl, May 2017
^ ^a ^b ^c GRCm38: Ensembl release 89: ENSMUSG00000030862 – Ensembl, May 2017
^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
^ "Entrez Gene: Carboxypeptidase X, M14 family member 2". Retrieved 2018-06-01.

Grupe A, Li Y, Rowland C, Nowotny P, Hinrichs AL, Smemo S, Kauwe JS, Maxwell TJ, Cherny S, Doil L, Tacey K, van Luchene R, Myers A, Wavrant-De Vrièze F, Kaleem M, Hollingworth P, Jehu L, Foy C, Archer N, Hamilton G, Holmans P, Morris CM, Catanese J, Sninsky J, White TJ, Powell J, Hardy J, O'Donovan M, Lovestone S, Jones L, Morris JC, Thal L, Owen M, Williams J, Goate A (January 2006). "A scan of chromosome 10 identifies a novel locus showing strong association with late-onset Alzheimer disease". Am. J. Hum. Genet. 78 (1): 78–88. doi:10.1086/498851. PMC 1380225. PMID 16385451.
Rose JE, Behm FM, Drgon T, Johnson C, Uhl GR (2010). "Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score". Mol. Med. 16 (7–8): 247–53. doi:10.2119/molmed.2009.00159. PMC 2896464. PMID 20379614.

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