Ensembl ID ENSG00000153187 Gene ID 3192 Accession 5048
Gene Symbol HNRNPU Alias SAFA;DEE54;HNRPU;SAF-A;U21.1;pp120;EIEE54;GRIP120;hnRNPU;HNRNPU-AS1 Full Name heterogeneous nuclear ribonucleoprotein U
Position 1 : 244840638 - 244864560 Length 23923 bases Strand Minus strand
Status Confidence Main interacting RNAsmRNARBP type Canonical_RBPs
Summary This gene encodes a member of a family of proteins that bind nucleic acids and function in the formation of ribonucleoprotein complexes in the nucleus with heterogeneous nuclear RNA (hnRNA). The encoded protein has affinity for both RNA and DNA, and binds scaffold-attached region (SAR) DNA. Mutations in this gene have been associated with epileptic encephalopathy, early infantile, 54. A pseudogene of this gene has been identified on chromosome 14. [provided by RefSeq, Jun 2017]

ENSG00000153187 Expression In 33 Tumors

Ensembl ID Gene symbol Log2 Foldchange Pvaue Cancer
ENSG00000153187 HNRNPU -0.2 2.29e-13 KIRC
ENSG00000153187 HNRNPU 0.55 1.70e-69 BRCA
ENSG00000153187 HNRNPU 0.43 2.59e-15 COAD
ENSG00000153187 HNRNPU 0.35 2.34e-11 LUSC
Ensembl ID Gene symbol Cancer types Pubmed ID
ENSG00000153187 HNRNPU tumor 10356358
ENSG00000153187 HNRNPU tumor 11694516
ENSG00000153187 HNRNPU cancer 12188916
ENSG00000153187 HNRNPU tumor 12665652
ENSG00000153187 HNRNPU tumour 16924231
ENSG00000153187 HNRNPU tumor 18772145
ENSG00000153187 HNRNPU tumor 20093774
ENSG00000153187 HNRNPU GBM 20668194
ENSG00000153187 HNRNPU tumor 21194727
ENSG00000153187 HNRNPU oral cancer 22259181
ENSG00000153187 HNRNPU breast cancer 24495796
ENSG00000153187 HNRNPU tumours 25406515
ENSG00000153187 HNRNPU tumor 26067913
ENSG00000153187 HNRNPU tumor 26506240
ENSG00000153187 HNRNPU Cancer 28622508
ENSG00000153187 HNRNPU tumour 28947659
ENSG00000153187 HNRNPU tumor 29228625
ENSG00000153187 HNRNPU tumor 29434445
ENSG00000153187 HNRNPU cancer 29511351
ENSG00000153187 HNRNPU pancreatic cancer 29657295
ENSG00000153187 HNRNPU prostate cancer 30177244
ENSG00000153187 HNRNPU gastric cancer 30336538
ENSG00000153187 HNRNPU colon cancer 31311954
ENSG00000153187 HNRNPU liver cancer 31331910
ENSG00000153187 HNRNPU tumor 31495606
Ensembl ID Gene symbol Disease/phenotype Mutation type Mutated / Total samples Literature
Ensembl ID Gene symbol Cancer P-value Which worse show
ENSG00000153187 HNRNPU MESO 0.0019 high
ENSG00000153187 HNRNPU SARC 0.048 high
ENSG00000153187 HNRNPU PAAD 0.02 high
ENSG00000153187 HNRNPU LGG 0.00024 high
ENSG00000153187 HNRNPU HNSC 0.042 high
ENSG00000153187 HNRNPU READ 0.013 low
ENSG00000153187 HNRNPU LUAD 0.00091 high
ENSG00000153187 HNRNPU THYM 0.011 low
ENSG00000153187 HNRNPU OV 0.047 low
ENSG00000153187 HNRNPU PRAD 0.0033 high
ENSG00000153187 HNRNPU TGCT 0.033 low
ENSG00000153187 HNRNPU BLCA 0.039 high
ENSG00000153187 HNRNPU GBM 0.025 low
ENSG00000153187 HNRNPU SKCM 0.035 low
Ensembl ID Gene symbol Cancer CNV type -log10(q-value) G-score average amplitude frequency
ENSG00000153187 HNRNPU LUAD Amp 1.869676 0.146485 0.503220 0.684109
ENSG00000153187 HNRNPU CESC Amp 1.232730 0.149636 0.589511 0.511864
ENSG00000153187 HNRNPU SARC Del 4.779471 0.212739 0.479230 0.291829
ENSG00000153187 HNRNPU GBM Amp 2.423455 0.097657 0.630704 0.164645
ENSG00000153187 HNRNPU ESCA Amp 0.888844 0.272231 0.511820 0.500000
ENSG00000153187 HNRNPU SKCM Amp 5.935928 0.265257 0.710570 0.553134
ENSG00000153187 HNRNPU LIHC Amp 7.255211 0.246091 0.839526 0.724324
ENSG00000153187 HNRNPU PCPG Del 0.885132 0.062820 0.537894 0.129630
ENSG00000153187 HNRNPU DLBC Del 1.770602 0.184953 0.511109 0.187500
ENSG00000153187 HNRNPU BRCA Amp 17.751877 0.331847 0.799913 0.737037
ENSG00000153187 HNRNPU UCEC Amp 3.125789 0.153209 0.865810 0.413729
ENSG00000153187 HNRNPU KIRC Del 0.682869 0.024196 0.458910 0.079545
ENSG00000153187 HNRNPU OV Amp 8.380275 0.517917 0.750751 0.533679