Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
23160
Gene name Gene Name - the full gene name approved by the HGNC.
WD repeat domain 43
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
WDR43
Synonyms (NCBI Gene) Gene synonyms aliases
NET12, UTP5
Chromosome Chromosome number
2
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
2p23.2
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT031487 hsa-miR-16-5p Proteomics 18668040
MIRT046118 hsa-miR-30b-5p CLASH 23622248
MIRT037019 hsa-miR-877-3p CLASH 23622248
MIRT1490569 hsa-miR-1185 CLIP-seq
MIRT1490570 hsa-miR-1207-3p CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000785 Component Chromatin ISS
GO:0000993 Function RNA polymerase II complex binding ISS
GO:0001650 Component Fibrillar center IDA 24219289
GO:0003711 Function Transcription elongation regulator activity ISS
GO:0003723 Function RNA binding HDA 22658674
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
616195 28945 ENSG00000163811
Protein
UniProt ID Q15061
Protein name WD repeat-containing protein 43 (U3 small nucleolar RNA-associated protein 5 homolog)
Protein function Ribosome biogenesis factor that coordinates hyperactive transcription and ribogenesis (PubMed:17699751). Part of the small subunit (SSU) processome, first precursor of the small eukaryotic ribosomal subunit. During the assembly of the SSU proces
PDB 7MQ8 , 7MQ9 , 7MQA
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00400 WD40 115 154 WD domain, G-beta repeat Repeat
PF00400 WD40 157 194 WD domain, G-beta repeat Repeat
PF04003 Utp12 473 577 Dip2/Utp12 Family Family
Sequence
MAAGGGGSCDPLAPAGVPCAFSPHSQAYFALASTDGHLRVWETANNRLHQEYVPSAHLSG
TCTCLAWAPARLQAKESPQRKKRKSEAVGMSNQTDLLALGTAVGSILLYSTVKGELHSKL
ISGGHDNRVNCIQWHQDSGCLYSCSDDKHIVEWN
VQTCKVKCKWKGDNSSVSSLCISPDG
KMLLSAGRTIKLWV
LETKEVYRHFTGHATPVSSLMFTTIRPPNESQPFDGITGLYFLSGA
VHDRLLNVWQVRSENKEKSAVMSFTVTDEPVYIDLTLSENKEEPVKLAVVCRDGQVHLFE
HILNGYCKKPLTSNCTIQIATPGKGKKSTPKPIPILAAGFCSDKMSLLLVYGSWFQPTIE
RVALNSREPHMCLVRDISNCWAPKVETAITKVRTPVMNSEAKVLVPGIPGHHAAIKPAPP
QTEQVESKRKSGGNEVSIEERLGAMDIDTHKKGKEDLQTNSFPVLLTQGLESNDFEMLNK
VLQTRNVNLIKKTVLRMPLHTIIPLLQELTKRLQGHPNSAVLMVQWLKCVLTVHASYLST
LPDLVPQLGTLYQLMESRVKTFQKLSHLHGKLILLIT
QVTASEKTKGATSPGQKAKLVYE
EESSEEESDDEIADKDSEDNWDEDEEESESEKDEDVEEEDEDAEGKDEENGEDRDTASEK
ELNGDSDLDPENESEEE
Sequence length 677
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG   Reactome
  Ribosome biogenesis in eukaryotes   Major pathway of rRNA processing in the nucleolus and cytosol
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Breast carcinoma Breast Carcinoma rs80359671, rs11540652, rs28934575, rs28897672, rs137886232, rs193922376, rs80357783, rs80359306, rs80359405, rs80359507, rs80359598, rs80358429, rs397507683, rs397515636, rs80359451
View all (71 more)
27117709
Unknown
Disease term Disease name Evidence References Source
Breast cancer Breast cancer Importantly, breast cancer patients bearing PRC2 LOF mutations displayed significantly worse prognosis compared with PRC2 wild-type patients GWAS, CBGDA
Oligodendroglioma Oligodendroglioma GWAS
Associations from Text Mining
Disease Name Relationship Type References
Breast Neoplasms Associate 27117709, 34803163
Colorectal Neoplasms Associate 29658574
Muscular Diseases Associate 39438952
Pulmonary Arterial Hypertension Associate 38110868
Sepsis Associate 39438952