Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
220988
Gene name Gene Name - the full gene name approved by the HGNC.
Heterogeneous nuclear ribonucleoprotein A3
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
HNRNPA3
Synonyms (NCBI Gene) Gene synonyms aliases
2610510D13Rik, D10S102, FBRNP, HNRPA3
Chromosome Chromosome number
2
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
2q31.2
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT020978 hsa-miR-155-5p Proteomics 19193853
MIRT020978 hsa-miR-155-5p Other 20584899
MIRT020978 hsa-miR-155-5p Proteomics 17881434
MIRT024046 hsa-miR-1-3p Proteomics 18668040
MIRT042699 hsa-miR-346 CLASH 23622248
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000398 Process MRNA splicing, via spliceosome IC 11991638
GO:0000398 Process MRNA splicing, via spliceosome TAS
GO:0003723 Function RNA binding HDA 22658674, 22681889
GO:0005515 Function Protein binding IPI 22720776, 26496610, 30021884
GO:0005634 Component Nucleus IDA 22720776
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
605372 24941 ENSG00000170144
Protein
UniProt ID P51991
Protein name Heterogeneous nuclear ribonucleoprotein A3 (hnRNP A3)
Protein function Plays a role in cytoplasmic trafficking of RNA. Binds to the cis-acting response element, A2RE. May be involved in pre-mRNA splicing.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00076 RRM_1 37 106 RNA recognition motif. (a.k.a. RRM, RBD, or RNP domain) Domain
PF00076 RRM_1 128 199 RNA recognition motif. (a.k.a. RRM, RBD, or RNP domain) Domain
Sequence
MEVKPPPGRPQPDSGRRRRRRGEEGHDPKEPEQLRKLFIGGLSFETTDDSLREHFEKWGT
LTDCVVMRDPQTKRSRGFGFVTYSCVEEVDAAMCARPHKVDGRVVE
PKRAVSREDSVKPG
AHLTVKKIFVGGIKEDTEEYNLRDYFEKYGKIETIEVMEDRQSGKKRGFAFVTFDDHDTV
DKIVVQKYHTINGHNCEVK
KALSKQEMQSAGSQRGRGGGSGNFMGRGGNFGGGGGNFGRG
GNFGGRGGYGGGGGGSRGSYGGGDGGYNGFGGDGGNYGGGPGYSSRGGYGGGGPGYGNQG
GGYGGGGGYDGYNEGGNFGGGNYGGGGNYNDFGNYSGQQQSNYGPMKGGSFGGRSSGSPY
GGGYGSGGGSGGYGSRRF
Sequence length 378
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG   Reactome
  Spliceosome
Amyotrophic lateral sclerosis
  mRNA Splicing - Major Pathway
Processing of Capped Intron-Containing Pre-mRNA
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Schizophrenia Schizophrenia rs13447324, rs387906932, rs387906933, rs863223354, rs863223355, rs776061422, rs863223349, rs748809996, rs759748655, rs863223353, rs863223350, rs863223356, rs781821239, rs863223348, rs863223346
View all (12 more)
16223876
Associations from Text Mining
Disease Name Relationship Type References
Alzheimer Disease Associate 30040709
Chromosome Breakage Associate 31642962
Frontotemporal Lobar Degeneration Associate 28431575
Glioblastoma Associate 29687002
Motor Neuron Disease Associate 28431575
Neurodegenerative Diseases Associate 30040709
Neuronal intranuclear inclusion disease Associate 36621630