Prame family member 10

PRAMEF10
Identifiers
Aliases	PRAMEF10, PRAME family member 10
External IDs	GeneCards: PRAMEF10
Gene location (Human)
Chr.	Chromosome 1 (human)
End	12,898,270 bp
RNA expression pattern
	Top expressed in
	liver; ; right lobe of liver;
	n/a
	More reference expression data
	n/a
Gene ontology
Molecular function	retinoic acid receptor binding;
Cellular component	cytoplasm;
Biological process	negative regulation of cell differentiation; negative regulation of apoptotic process; negative regulation of transcription, DNA-templated; positive regulation of cell population proliferation;
	Sources:Amigo / QuickGO
Orthologs
Databases	NCBI: entry; OMA: entry
	343071
	n/a
	ENSG00000282663; ENSG00000187545
	n/a
	O60809
	n/a
	NM_001039361
	n/a
	NP_001034450
	n/a
	Wikidata
View/Edit Human

PRAME family member 10 is a protein that in humans is encoded by the PRAMEF10 gene.^[3] Not much has been reported about this protein’s function, but it is predicted to be involved in ubiquitylation.^[3]

References

1 2 3 ENSG00000187545 GRCh38: Ensembl release 89: ENSG00000282663, ENSG00000187545 – Ensembl, May 2017
↑ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
1 2 "Entrez Gene: PRAME family member 10". Retrieved 2016-05-29.

[refGRCh38Ensembl-1] 1 2 3 ENSG00000187545 GRCh38: Ensembl release 89: ENSG00000282663, ENSG00000187545 – Ensembl, May 2017

[2] "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.

[entrez-3] 1 2 "Entrez Gene: PRAME family member 10". Retrieved 2016-05-29.

[1]

[2]

[3]

See also

References