Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
6123
Gene name Gene Name - the full gene name approved by the HGNC.
Ribosomal protein L3 like
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
RPL3L
Synonyms (NCBI Gene) Gene synonyms aliases
CMD2D
Disease Acronyms (UniProt) Disease acronyms from UniProt database
CMD2D
Chromosome Chromosome number
16
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
16p13.3
Summary Summary of gene provided in NCBI Entrez Gene.
This gene encodes a protein that shares sequence similarity with ribosomal protein L3. The protein belongs to the L3P family of ribosomal proteins. Unlike the ubiquitous expression of ribosomal protein genes, this gene has a tissue-specific pattern of exp
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT621012 hsa-miR-3613-3p HITS-CLIP 23824327
MIRT611851 hsa-miR-6728-3p HITS-CLIP 23824327
MIRT611850 hsa-miR-767-3p HITS-CLIP 23824327
MIRT611849 hsa-miR-6828-3p HITS-CLIP 23824327
MIRT611856 hsa-miR-548ac HITS-CLIP 23824327
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000027 Process Ribosomal large subunit assembly IBA 21873635
GO:0003723 Function RNA binding IBA 21873635
GO:0003735 Function Structural constituent of ribosome IBA 21873635
GO:0003735 Function Structural constituent of ribosome NAS 12962325
GO:0005840 Component Ribosome TAS 8921388
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
617416 10351 ENSG00000140986
Protein
UniProt ID Q92901
Protein name Ribosomal protein uL3-like (60S ribosomal protein L3-like) (Large ribosomal subunit protein uL3-like)
Protein function Heart- and skeletal muscle-specific component of the ribosome, which regulates muscle function. Component of the large ribosomal subunit in striated muscle cells: replaces the RPL3 paralog in the ribosome in these cells. The ribosome is a large
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00297 Ribosomal_L3 1 375 Ribosomal protein L3 Family
Sequence
Sequence length 407
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  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)
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Atrial fibrillation Atrial Fibrillation rs120074192, rs121908590, rs121908593, rs121434558, rs587776851, rs387906612, rs387906613, rs387906614, rs387906615, rs199472687, rs199472705, rs199473324, rs587777336, rs587777339, rs587777557
View all (6 more)
29892015, 30061737
Unknown
Disease term Disease name Evidence References Source
Paroxysmal atrial fibrillation Paroxysmal atrial fibrillation 30061737 ClinVar
Myopathy dilated cardiomyopathy GenCC
Cardiomyopathy cardiomyopathy, dilated, 2D GenCC
Atrial Fibrillation Atrial Fibrillation GWAS
Associations from Text Mining
Disease Name Relationship Type References
Azoospermia Inhibit 36589848
Cardiomyopathy Dilated Associate 32514796
Colonic Neoplasms Associate 35712285
Hearing Loss Associate 33078831
Oligospermia Associate 36589848
Syndrome Associate 36589848