Ensembl ID ENSG00000119969 Gene ID 3070 Accession 4861
Gene Symbol HELLS Alias LSH;ICF4;PASG;SMARCA6;Nbla10143 Full Name helicase, lymphoid specific
Position 10 : 94545329 - 94613905 Length 68577 bases Strand Plus strand
Status Confidence Main interacting RNAsN.A.RBP type Canonical_RBPs
Summary This gene encodes a lymphoid-specific helicase. Other helicases function in processes involving DNA strand separation, including replication, repair, recombination, and transcription. This protein is thought to be involved with cellular proliferation and may play a role in leukemogenesis. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jan 2014]

ENSG00000119969 Expression In 33 Tumors

Ensembl ID Gene symbol Log2 Foldchange Pvaue Cancer
ENSG00000119969 1.09 1.10e-16 HNSC
ENSG00000119969 1.60 1.57e-18 BLCA
ENSG00000119969 1.74 3.44e-84 BRCA
ENSG00000119969 1.58 1.92e-30 COAD
ENSG00000119969 3.10 2.23e-173 LUSC
ENSG00000119969 2.43 1.35e-40 LIHC
ENSG00000119969 1.94 3.81e-38 STAD
ENSG00000119969 1.58 1.25e-26 UCEC
ENSG00000119969 2.56 2.82e-18 CHOL
ENSG00000119969 3.61 8.04e-25 CESC
ENSG00000119969 2.38 2.22e-68 LUAD
Ensembl ID Gene symbol Cancer types Pubmed ID
ENSG00000119969 tumor 15105378
ENSG00000119969 Tumor 15305370
ENSG00000119969 tumor 15611660
ENSG00000119969 oral cancer 19287496
ENSG00000119969 cancer 20400365
ENSG00000119969 tumor 22109759
ENSG00000119969 tumours 22157815
ENSG00000119969 HNSCC 22461910
ENSG00000119969 tumor 25338120
ENSG00000119969 tumors 27191985
ENSG00000119969 cancer 27302170
ENSG00000119969 cancer 28069330
ENSG00000119969 lung cancer 29037212
ENSG00000119969 tumor 30042885
ENSG00000119969 cancer 30094095
ENSG00000119969 cancers 30220967
ENSG00000119969 Tumor 30516846
ENSG00000119969 tumor 30779712
ENSG00000119969 cancers 31066149
ENSG00000119969 tumor 31253190
ENSG00000119969 tumor 31541170
ENSG00000119969 cancer 31594538
ENSG00000119969 cancers 31802118
ENSG00000119969 cancer 6665873
Ensembl ID Gene symbol Disease/phenotype Mutation type Mutated / Total samples Literature
Ensembl ID Gene symbol Cancer P-value Which worse show
ENSG00000119969 SARC 0.0019 high
ENSG00000119969 STAD 0.023 low
ENSG00000119969 CHOL 0.017 high
ENSG00000119969 PAAD 0.0067 high
ENSG00000119969 UCEC 0.028 low
ENSG00000119969 LUSC 0.00012 low
ENSG00000119969 HNSC 0.007 low
ENSG00000119969 READ 0.022 high
ENSG00000119969 LUAD 0.00057 high
ENSG00000119969 PCPG 0.005 high
ENSG00000119969 THYM 0.0012 low
ENSG00000119969 UCS 0.0076 low
ENSG00000119969 ESCA 0.029 high
ENSG00000119969 PRAD 0.00025 high
ENSG00000119969 BLCA 0.037 low
ENSG00000119969 LAML 0.028 high
ENSG00000119969 GBM 0.048 low
ENSG00000119969 CESC 0.00023 low
Ensembl ID Gene symbol Cancer CNV type -log10(q-value) G-score average amplitude frequency
ENSG00000119969 LUSC Del 0.716583 0.065694 0.360106 0.520958
ENSG00000119969 COAD Del 6.918174 0.093622 0.397311 0.232816
ENSG00000119969 GBM Del 0.607584 0.050474 0.695748 0.887348
ENSG00000119969 HNSC Del 1.957544 0.068029 0.347760 0.260536
ENSG00000119969 LIHC Del 0.787865 0.066715 0.480248 0.262162
ENSG00000119969 BLCA Del 1.572330 0.092078 0.396474 0.409314
ENSG00000119969 BRCA Del 3.039428 0.081600 0.369009 0.292593
ENSG00000119969 STAD Del 3.609291 0.095990 0.378192 0.240363
ENSG00000119969 PRAD Del 3.774375 0.105184 0.424302 0.178862
ENSG00000119969 UCEC Del 7.658899 0.105855 0.546996 0.153989
ENSG00000119969 MESO Del 1.128840 0.141864 0.486274 0.321839
ENSG00000119969 OV Del 10.777835 0.307218 0.553201 0.417962