Pejvakin

PJVK
Identifiers
Aliases	PJVK, DFNB59, deafness, autosomal recessive 59, pejvakin
External IDs	OMIM: 610219; MGI: 2685847; HomoloGene: 19773; GeneCards: PJVK; OMA:PJVK - orthologs
Gene location (Human)
Chr.	Chromosome 2 (human)
End	178,462,102 bp
Gene location (Mouse)
Chr.	Chromosome 2 (mouse)
End	76,488,900 bp
RNA expression pattern
	Top expressed in
	sperm; ; right testis; ; left testis; ; left ovary; ; anterior pituitary; ; right ovary; ; right lobe of liver; ; Brodmann area 9; ; C1 segment; ; left lobe of thyroid gland;
	Top expressed in
	embryo; ; embryo; ; proximal tubule; ; genital tubercle; ; ventricular zone; ; tail of embryo; ; islet of Langerhans; ; Mesencephalon; ; right kidney; ; human kidney;
	More reference expression data
	n/a
Orthologs
	494513
	381375
	ENSG00000204311
	ENSMUSG00000075267
	Q0ZLH3
	Q0ZLH2
NM_001042702; NM_001353775; NM_001353776; NM_001353777; NM_001353778;
	NM_001369912
	NM_001080711
NP_001036167; NP_001340704; NP_001340705; NP_001340706; NP_001340707;
	NP_001356841
	NP_001074180
	Wikidata
View/Edit Human	View/Edit Mouse

Pejvakin is a protein that in humans is encoded by the PJVK gene.