Gene Gene information from NCBI Gene database.
Entrez ID 23185
Gene name La ribonucleoprotein 4B
Gene symbol LARP4B
Synonyms (NCBI Gene)
KIAA0217LARP5
Chromosome 10
Chromosome location 10p15.3
Summary This gene encodes a member of an evolutionarily conserved protein family implicated in RNA metabolism and translation. Members of this family are characterized by the presence of an La motif, which is often located adjacent to one or more RNA recognition
miRNA miRNA information provided by mirtarbase database.
1208
miRTarBase ID miRNA Experiments Reference
MIRT027047 hsa-miR-103a-3p Sequencing 20371350
MIRT028584 hsa-miR-30a-5p Proteomics 18668040
MIRT032113 hsa-let-7d-5p Sequencing 20371350
MIRT611360 hsa-miR-6776-3p HITS-CLIP 23824327
MIRT611358 hsa-miR-191-3p HITS-CLIP 23824327
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
20
GO ID Ontology Definition Evidence Reference
GO:0003676 Function Nucleic acid binding IEA
GO:0003723 Function RNA binding HDA 22658674, 22681889
GO:0003723 Function RNA binding IEA
GO:0003730 Function MRNA 3'-UTR binding IBA
GO:0003730 Function MRNA 3'-UTR binding IDA 26001795
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
616513 28987 ENSG00000107929
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q92615
Protein name La-related protein 4B (La ribonucleoprotein domain family member 4B) (La ribonucleoprotein domain family member 5) (La-related protein 5)
Protein function Stimulates mRNA translation.
PDB 3PTH
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF05383 La 160 216 La domain Domain
Sequence
MTSDQDAKVVAEPQTQRVQEGKDSAHLMNGPISQTTSQTSSIPPLSQVPATKVSELNPNA
EVWGAPVLHLEASSAADGVSAAWEEVAGHHADRGPQGSDANGDGDQGHENAALPDPQESD
PADMNALALGPSEYDSLPENSETGGNESQPDSQEDPREVLKKTLEFCLSRENLASDMYLI
SQMDSDQYVPITTVANLDHIKKLSTDVDLIVEVLRS
LPLVQVDEKGEKVRPNQNRCIVIL
REISESTPVEEVEALFKGDNLPKFINCEFAYNDNWFITFETEADAQQAYKYLREEVKTFQ
GKPIKARIKAKAIAINTFLPKNGFRPLDVSLYAQQRYATSFYFPPMYSPQQQFPLYSLIT
PQTWSATHSYLDPPLVTPFPNTGFINGFTSPAFKPAASPLTSLRQYPPRSRNPSKSHLRH
AIPSAERGPGLLESPSIFNFTADRLINGVRSPQTRQAGQTRTRIQNPSAYAKREAGPGRV
EPGSLESSPGLGRGRKNSFGYRKKREEKFTSSQTQSPTPPKPPSPSFELGLSSFPPLPGA
AGNLKTEDLFENRLSSLIIGPSKERTLSADASVNTLPVVVSREPSVPASCAVSATYERSP
SPAHLPDDPKVAEKQRETHSVDRLPSALTATACKSVQVNGAATELRKPSYAEICQRTSKE
PPSSPLQPQKEQKPNTVGCGKEEKKLAEPAERYREPPALKSTPGAPRDQRRPAGGRPSPS
AMGKRLSREQSTPPKSPQ
Sequence length 738
Interactions View interactions
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
4
Causal Diseases associated with Pathogenic or Likely Pathogenic variants in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Myoepithelial tumor Likely pathogenic rs2491229815 RCV002463924
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Autism spectrum disorder association rs1832871459 RCV001291390
Lung cancer Benign rs144883024 RCV005903118
Thyroid cancer, nonmedullary, 1 Benign rs144883024 RCV005903117
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Carcinogenesis Associate 37356415
Carcinoma Hepatocellular Associate 31772683
Glioma Associate 34482648, 36552760
Neoplasms Associate 31772683
Neoplasms Inhibit 37356415
Prostatic Neoplasms Associate 31173237
Stomach Neoplasms Associate 28649990