C19orf22

R3HDM4
Identifiers
Aliases	R3HDM4, C19orf22, R3H domain containing 4
External IDs	MGI: 1924814; HomoloGene: 16343; GeneCards: R3HDM4; OMA:R3HDM4 - orthologs
Gene location (Human)
Chr.	Chromosome 19 (human)
End	913,245 bp
Gene location (Mouse)
Chr.	Chromosome 10 (mouse)
End	79,757,042 bp
RNA expression pattern
	Top expressed in
	blood; ; secondary oocyte; ; pancreatic ductal cell; ; granulocyte; ; beta cell; ; mucosa of ileum; ; mononuclear cell; ; monocyte; ; spleen; ; bone marrow;
	Top expressed in
	granulocyte; ; primary visual cortex; ; superior frontal gyrus; ; dentate gyrus of hippocampal formation granule cell; ; ascending aorta; ; aortic valve; ; muscle of thigh; ; lip; ; zygote; ; blood;
	More reference expression data
	n/a
Orthologs
	91300
	109284
	ENSG00000198858
	ENSMUSG00000035781
	Q96D70
	Q4VBF2
	NM_138774
	NM_177994; NM_001378997
	NP_620129
	NP_818775; NP_001365926
	Wikidata
View/Edit Human	View/Edit Mouse

Chromosome 19 open reading frame 22 (c19orf22) is a protein which in humans is encoded by the c19orf22 gene. The primary alias of the gene is R3H domain containing 4 (R3HDM4), but it is commonly referred to as c19orf22.