Gene Details | GeDiPNet - Complete Gene Info, Disease Associations & Pathways

Gene Gene miRNA Gene ontology Other IDs Protein Pathways Associated diseases
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.	6144
Gene name Gene Name - the full gene name approved by the HGNC.	Ribosomal protein L21
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.	RPL21
Synonyms (NCBI Gene) Gene synonyms aliases	HYPT12, L21, eL21
Disease Acronyms (UniProt) Disease acronyms from UniProt database	HYPT12
Chromosome Chromosome number	13
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.	13q12.2
Summary Summary of gene provided in NCBI Entrez Gene.	Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal pro

Show/Hide all(14)

miRTarBase ID	miRNA	Experiments	Reference
MIRT031954	hsa-miR-16-5p	Proteomics	18668040
MIRT050909	hsa-miR-17-5p	CLASH	23622248
MIRT050593	hsa-miR-20a-5p	CLASH	23622248
MIRT048563	hsa-miR-100-5p	CLASH	23622248
MIRT046903	hsa-miR-221-3p	CLASH	23622248
MIRT045855	hsa-miR-128-3p	CLASH	23622248
MIRT044294	hsa-miR-106b-5p	CLASH	23622248
MIRT042180	hsa-miR-484	CLASH	23622248
MIRT040024	hsa-miR-615-3p	CLASH	23622248
MIRT039492	hsa-miR-652-3p	CLASH	23622248
MIRT439741	hsa-miR-218-5p	HITS-CLIP	23212916
MIRT439741	hsa-miR-218-5p	HITS-CLIP	23212916
MIRT1316221	hsa-miR-4257	CLIP-seq
MIRT1316221	hsa-miR-4257	CLIP-seq

Show/Hide all(14)

GO ID	Ontology	Definition	Evidence	Reference
GO:0000184	Process	Nuclear-transcribed mRNA catabolic process, nonsense-mediated decay	TAS
GO:0003723	Function	RNA binding	HDA	22658674, 22681889
GO:0003735	Function	Structural constituent of ribosome	IBA	21873635
GO:0003735	Function	Structural constituent of ribosome	NAS	12962325
GO:0005515	Function	Protein binding	IPI	24965446
GO:0005783	Component	Endoplasmic reticulum	IEA
GO:0005829	Component	Cytosol	TAS
GO:0006412	Process	Translation	NAS	12962325
GO:0006413	Process	Translational initiation	TAS
GO:0006614	Process	SRP-dependent cotranslational protein targeting to membrane	TAS
GO:0016020	Component	Membrane	HDA	19946888
GO:0019083	Process	Viral transcription	TAS
GO:0022625	Component	Cytosolic large ribosomal subunit	HDA	12962325
GO:0022625	Component	Cytosolic large ribosomal subunit	IBA	21873635

MIM	HGNC	e!Ensembl
603636	10313	ENSG00000122026

Protein

UniProt ID

P46778

Protein name

Large ribosomal subunit protein eL21 (60S ribosomal protein L21)

Protein function

Component of the large ribosomal subunit (PubMed:12962325, PubMed:23636399, PubMed:25901680, PubMed:25957688). The ribosome is a large ribonucleoprotein complex responsible for the synthesis of proteins in the cell (PubMed:12962325, PubMed:23636

PDB

4UG0 , 4V6X , 5AJ0 , 5LKS , 5T2C , 6IP5 , 6IP6 , 6IP8 , 6LQM , 6LSR , 6LSS , 6LU8 , 6OLE , 6OLF , 6OLG , 6OLI , 6OLZ , 6OM0 , 6OM7 , 6QZP , 6W6L , 6XA1 , 6Y0G , 6Y2L , 6Y57 , 6Y6X , 6Z6L , 6Z6M , 6Z6N , 6ZM7 , 6ZME , 6ZMI , 6ZMO , 7BHP , 7F5S , 7OW7 , 7QVP , 7XNX , 7XNY , 8A3D , 8FKP , 8FKQ , 8FKR , 8FKS , 8FKT , 8FKU , 8FKV , 8FKW , 8FKX , 8FKY , 8FKZ

Family and domains

Pfam

Accession	ID	Position in sequence	Description	Type
PF01157	Ribosomal_L21e	1 → 101	Ribosomal protein L21e	Family

Sequence

MTNTKGKRRGTRYMFSRPFRKHGVVPLATYMRIYKKGDIVDIKGMGTVQKGMPHKCYHGK
TGRVYNVTQHAVGIVVNKQVKGKILAKRINVRIEHIKHSKSRDSFLKRVKENDQKKKEAK
EKGTWVQLKRQPAPPREAHFVRTNGKEPELLEPIPYEFMA

Sequence length

160

Interactions

View interactions

	KEGG		Reactome
	Ribosome Coronavirus disease - COVID-19		L13a-mediated translational silencing of Ceruloplasmin expression SRP-dependent cotranslational protein targeting to membrane Viral mRNA Translation Major pathway of rRNA processing in the nucleolus and cytosol Formation of a pool of free 40S subunits GTP hydrolysis and joining of the 60S ribosomal subunit Nonsense Mediated Decay (NMD) independent of the Exon Junction Complex (EJC) Nonsense Mediated Decay (NMD) enhanced by the Exon Junction Complex (EJC)

Show/Hide Causal Diseases (2)

Disease term	Disease name	dbSNP ID	References
Causal
Hypotrichosis	Hypotrichosis, HYPOTRICHOSIS 12	rs121434306, rs121434307, rs121434308, rs121434309, rs1325804776, rs267606775, rs786200875, rs1568062215, rs267606776, rs1462595806, rs267606777, rs267606659, rs2147483647, rs559648418, rs121917819 View all (18 more)	21412954
Hypotrichosis simplex	Hypotrichosis simplex	rs121913026, rs201249971	21412954

Show/Hide Text Mining Associations (7)

Disease Name	Relationship Type	References
Associations from Text Mining
Alzheimer Disease	Associate	37545529, 38176923
Anemia Diamond Blackfan	Associate	20116044
Cataract	Associate	11773032
Cholangiocarcinoma	Associate	35732325
Hypertension	Associate	32888289
Nasopharyngeal Carcinoma	Associate	16308470
Squamous Cell Carcinoma of Head and Neck	Associate	36550360

RPL21 (ribosomal protein L21)