Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
55152
Gene name Gene Name - the full gene name approved by the HGNC.
DALR anticodon binding domain containing 3
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
DALRD3
Synonyms (NCBI Gene) Gene synonyms aliases
DEE86, EIEE86
Disease Acronyms (UniProt) Disease acronyms from UniProt database
DEE86
Chromosome Chromosome number
3
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
3p21.31
Summary Summary of gene provided in NCBI Entrez Gene.
The exact function of this gene is not known. It encodes a protein with a DALR anticodon binding domain similar to that of class Ia aminoacyl tRNA synthetases. This gene is located in a cluster of genes (with a complex sense-anti-sense genome architecture
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT040896 hsa-miR-18a-3p CLASH 23622248
MIRT1973452 hsa-miR-129-5p CLIP-seq
MIRT1973453 hsa-miR-3140-3p CLIP-seq
MIRT1973454 hsa-miR-629 CLIP-seq
MIRT2447995 hsa-miR-101 CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0004814 Function Arginine-tRNA ligase activity IEA
GO:0005515 Function Protein binding IPI 25416956
GO:0005524 Function ATP binding IEA
GO:0006420 Process Arginyl-tRNA aminoacylation IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
618904 25536 ENSG00000178149
Protein
UniProt ID Q5D0E6
Protein name DALR anticodon-binding domain-containing protein 3
Protein function Involved in tRNA methylation. Facilitates the recognition and targeting of tRNA(Arg)(CCU) and tRNA(Arg)(UCU) substrates for N(3)-methylcytidine modification by METTL2A and METTL2B.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF05746 DALR_1 403 543 DALR anticodon binding domain Domain
Sequence
MATRRLGVGETLGALNAALGPGGPVWIKETRTRHLRSRDFLAPHRALQARFDDGQVPEHL
LHALACLQGPGVAPVLRCAPTPAGLSLQLQRSAVFERVLSAVAAYATPASPASLGQRVLL
HCPALRSSPCALRLSQLRTVLVADHLARALRAHGVCVRLVPAVRDPHMLTFLQQLRVDWP
AASERASSHTLRSHALEELTSANDGRTLSPGILGRLCLKELVEEQGRTAGYDPNLDNCLV
TEDLLSVLAELQEALWHWPEDSHPGLAGASDTGTGGCLVVHVVSCEEEFQQQKLDLLWQK
LVDKAPLRQKHLICGPVKVAGAPGTLMTAPEYYEFRHTQVCKASALKHGGDLAQDPAWTE
IFGVLSVATIKFEMLSTAPQSQLFLALADSSISTKGTKSGTFVMYNCARLATLFESYKCS
MEQGLYPTFPPVSSLDFSLLHDEGEWLLLFNSILPFPDLLSRTAVLDCTAPGLHIAVRTE
MICKFLVQLSMDFSSYYNRVHILGEPRPHLFGQMFVRLQLLRAVREVLHTGLAMLGLPPL
SHI
Sequence length 543
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Mitochondrial complex deficiency MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 18 rs267606829, rs267606830, rs587776513, rs121918134, rs121918135, rs121918136, rs137853192, rs137853193, rs183973249, rs137853184, rs118203929, rs267606689, rs11544803, rs63751061, rs137852863
View all (210 more)
Unknown
Disease term Disease name Evidence References Source
Epileptic encephalopathy undetermined early-onset epileptic encephalopathy GenCC
Developmental And Epileptic Encephalopathy developmental and epileptic encephalopathy, 86 GenCC
Myocardial Infarction Myocardial Infarction GWAS
Associations from Text Mining
Disease Name Relationship Type References
Brain Diseases Associate 32427860
Developmental Disabilities Associate 32427860