UEVLD

UEVLD
Available structures
PDB	Ortholog search: PDBe RCSB
List of PDB id codes
	2I6T, 3DL2
Identifiers
Aliases	UEVLD, ATTP, UEV3, UEV and lactate/malate dehyrogenase domains
External IDs	OMIM: 610985 MGI: 1860490 HomoloGene: 69251 GeneCards: UEVLD
Gene location (Human)
Chr.	Chromosome 11 (human)[1]
End	18,588,747 bp[1]
Gene location (Mouse)
Chr.	Chromosome 7 (mouse)[2]
End	46,608,275 bp[2]
RNA expression pattern
	Top expressed in
	biceps brachii; ; myometrium; ; adipose tissue; ; Achilles tendon; ; seminal vesicula;
	More reference expression data
	n/a
Gene ontology
Molecular function	oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor; oxidoreductase activity; catalytic activity; molecular function;
Cellular component	extracellular exosome;
Biological process	protein transport; cellular protein modification process; carboxylic acid metabolic process; carbohydrate metabolic process; biological process;
	Sources:Amigo / QuickGO
Orthologs
	55293
	54122
	ENSG00000151116
	ENSMUSG00000043262
	Q8IX04
	Q3U1V6
NM_001040697; NM_001040698; NM_001261382; NM_001261383; NM_001261384;
	NM_001261385; NM_001261386; NM_001297771; NM_018314
	NM_001040695; NM_016855
NP_001035787; NP_001248311; NP_001248312; NP_001248313; NP_001248314;
	NP_001248315; NP_001284700; NP_060784
	NP_001035785
	Wikidata
View/Edit Human	View/Edit Mouse

UEV and lactate/malate dehyrogenase domains is a protein that in humans is encoded by the UEVLD gene. [5]

References

GRCh38: Ensembl release 89: ENSG00000151116 - Ensembl, May 2017
GRCm38: Ensembl release 89: ENSMUSG00000043262 - 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: UEV and lactate/malate dehyrogenase domains". Retrieved 2018-04-10.

PDBe-KB provides an overview of all the structure information available in the PDB for Human Ubiquitin-conjugating enzyme E2 variant 3

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