Ensembl ID ENSG00000071462 Gene ID 114049 Accession 16405
Gene Symbol BUD23 Alias WBMT;MERM1;PP3381;HUSSY-3;WBSCR22;HASJ4442 Full Name BUD23 rRNA methyltransferase and ribosome maturation factor
Position 7 : 73683597 - 73698212 Length 14616 bases Strand Plus strand
Status Confidence Main interacting RNAsN.A.RBP type Non-canonical_RBPs
Summary This gene encodes a protein containing a nuclear localization signal and an S-adenosyl-L-methionine binding motif typical of methyltransferases, suggesting that the encoded protein may act on DNA methylation. This gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. Alternatively spliced transcript variants have been found. [provided by RefSeq, Feb 2011]

ENSG00000071462 Expression In 33 Tumors

Ensembl ID Gene symbol Log2 Foldchange Pvaue Cancer
ENSG00000071462 0.81 1.10e-44 BRCA
ENSG00000071462 0.87 7.90e-28 COAD
ENSG00000071462 0.81 4.49e-29 LUSC
ENSG00000071462 0.68 3.09e-14 KIRP
ENSG00000071462 0.89 7.65e-20 UCEC
ENSG00000071462 0.79 2.97e-26 LUAD
Ensembl ID Gene symbol Cancer types Pubmed ID
ENSG00000071462 cancer 24086612
ENSG00000071462 cancer 24488492
ENSG00000071462 cancer 24763612
ENSG00000071462 cancers 26214185
ENSG00000071462 cancer 27207652
ENSG00000071462 colorectal cancer 29133897
ENSG00000071462 colorectal cancer 29888105
Ensembl ID Gene symbol Disease/phenotype Mutation type Mutated / Total samples Literature
Ensembl ID Gene symbol Cancer P-value Which worse show
ENSG00000071462 MESO 0.045 high
ENSG00000071462 STAD 0.03 low
ENSG00000071462 UCEC 0.00059 high
ENSG00000071462 ACC 0.025 high
ENSG00000071462 LUSC 0.028 low
ENSG00000071462 HNSC 0.022 high
ENSG00000071462 KIRP 0.026 low
ENSG00000071462 KICH 0.033 high
ENSG00000071462 LUAD 0.014 high
ENSG00000071462 BRCA 0.026 low
ENSG00000071462 COAD 0.011 high
ENSG00000071462 DLBC 0.00064 low
ENSG00000071462 BLCA 0.0022 low
ENSG00000071462 LAML 0.016 low
ENSG00000071462 GBM 0.0011 high
ENSG00000071462 SKCM 0.0051 low
ENSG00000071462 LIHC 0.00071 high
Ensembl ID Gene symbol Cancer CNV type -log10(q-value) G-score average amplitude frequency
ENSG00000071462 TGCT Amp 1.244648 0.142598 0.541014 0.793333