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TissGeneSummary for HRASLS |
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Basic gene information | Gene symbol | HRASLS |
Gene name | HRAS-like suppressor | |
Synonyms | A-C1|H-REV107|HRASLS1|HRSL1|HSD28 | |
Cytomap | UCSC genome browser: 3q29 | |
Type of gene | protein-coding | |
RefGenes | NM_020386.4, | |
Description | H-REV107 protein-related proteinHRAS-like suppressor 1phospholipase Aphospholipid-metabolizing enzyme A-C1 | |
Modification date | 20141207 | |
dbXrefs | MIM : 606487 | |
HGNC : HGNC | ||
Ensembl : ENSG00000127252 | ||
HPRD : 07577 | ||
Vega : OTTHUMG00000156104 | ||
Protein | UniProt: go to UniProt's Cross Reference DB Table | |
Expression | CleanEX: HS_HRASLS | |
BioGPS: 57110 | ||
Pathway | NCI Pathway Interaction Database: HRASLS | |
KEGG: HRASLS | ||
REACTOME: HRASLS | ||
Pathway Commons: HRASLS | ||
Context | iHOP: HRASLS | |
ligand binding site mutation search in PubMed: HRASLS | ||
UCL Cancer Institute: HRASLS | ||
Assigned class in TissGDB* | C | |
Included tissue-specific gene expression resources | TiGER,GTEx | |
Specific-tissues in normal samples (assigned by TissGDB using HPA, TiGER, and GTEx) | OvaryTestis | |
Cancer types related to the specific-tissues in cancer samples (assigned by TissGDB using TCGA) | OVTGCT | |
Reference showing the relevant tissue of HRASLS | ||
Description by TissGene annotations | Protective TissGene in OS |
* Class A consists of genes with literature evidence and is part of the cTissGenes. Class B consists of only cTissGenes without additional evidence. The remaining genes belong to Class C. |
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GO ID | GO term | PubMed ID |
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TissGeneExp for HRASLS |
![]() (TCGA IlluminaHiSeq_RNASeqV2, pan-cancer normalized log2(norm_counts+1) data, version 2016-08-16) |
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![]() (TCGA pan-cancer tcga_rsem_isoform_tpm, version 2016-09-01) |
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![]() (GTEx GTEx_Analysis_v6_RNA-seq_RNA-SeQCv1.1.8_gene_rpkm.gct) - Here, we shows the matched tissue types only among our 28 cancer types. |
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![]() (TCGA IlluminaHiSeq_RNASeqV2, pan-cancer normalized log2(norm_counts+1) data, version 2016-08-16) |
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- Significantly differentially expressed cancer types and information. (|Fold change|>1 and FDR<0.05) |
Cancer type | Mean(exp) in tumor | Mean(exp) in matched normal | Log2FC | P-val. | FDR |
LUSC | 0.741260547 | -2.324468865 | 3.065729412 | 1.74E-13 | 8.77E-13 |
HNSC | -0.316308172 | 1.727554619 | -2.043862791 | 7.81E-07 | 6.08E-06 |
LUAD | -0.540913625 | -2.498660177 | 1.957746552 | 6.49E-10 | 3.50E-09 |
STAD | -2.546407591 | -0.652313841 | -1.89409375 | 0.000165 | 0.001181799 |
PRAD | -4.085384514 | -2.966840283 | -1.118544231 | 0.000187 | 0.000743027 |
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TissGene-miRNA for HRASLS |
![]() (Gene-miRNA relations from TargetScanHuman Relsease 7.1, Conserved_Site_Context_Scores.txt.zip, 06.01.2016) (TCGA IlluminaHiSeq_miRNASeq, log2(RPM+1) data, version 2016-11-21) (TCGA IlluminaHiSeq_RNASeqV2, log2(normalized_count+1) data, version 2016-08-16) (Spearman’s Rank Correlation (p-value<0.05 and coefficient<-0.25)) |
Cancer type | miRNA id | miRNA accession | P-val. | Coeff. | # samples |
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TissGeneMut for HRASLS |
TissGeneSNV for HRASLS |
![]() Different colors of circles represent different cancer types. Circle size denotes number of samples. (TCGA somatic mutation (SNPs and small INDELs) data, version 2016-04-25) * Click on the image to enlarge it in a new window. |
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![]() (X-axis: cancer type and Y-axis: % of mutated samples) The numbers in parentheses are numbers of samples with mutation (nsSNVs). (TCGA somatic mutation (SNPs and small INDELs) data, version 2016-04-25) |
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- nsSNVs sorted by frequency. |
AAchange | Cancer type | # samples |
p.E127K | PAAD | 1 |
p.P15L | STAD | 1 |
p.P94S | HNSC | 1 |
p.A254D | STAD | 1 |
p.R127C | COAD | 1 |
p.R130C | PRAD | 1 |
p.D87Y | LUSC | 1 |
p.D87H | HNSC | 1 |
p.E214K | SKCM | 1 |
p.E22K | PAAD | 1 |
p.A216P | ESCA | 1 |
p.F24S | COAD | 1 |
p.P199S | HNSC | 1 |
p.E193K | BLCA | 1 |
p.Y11H | COAD | 1 |
p.H121R | LUSC | 1 |
p.A149D | STAD | 1 |
p.R130C | SKCM | 1 |
p.R243G | BLCA | 1 |
p.G123E | SKCM | 1 |
p.F227S | HNSC | 1 |
p.V143I | BRCA | 1 |
p.E103* | CESC | 1 |
p.R232C | SKCM | 1 |
p.D178N | SKCM | 1 |
p.R243* | SKCM | 1 |
p.P94L | UCEC | 1 |
p.N115Y | SKCM | 1 |
p.D192H | HNSC | 1 |
p.G181E | SKCM | 1 |
p.V150D | PAAD | 1 |
p.P117S | SKCM | 1 |
p.A2V | UCEC | 1 |
p.I148K | SKCM | 1 |
p.R25H | READ | 1 |
p.Y144D | HNSC | 1 |
p.E22K | UCEC | 1 |
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TissGeneCNV for HRASLS |
![]() (TCGA Gistic2_CopyNumber_Gistic2_all_data_by_genes, Gistic2 copy number data, version 2016-08-16) |
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TissGeneFusions for HRASLS |
![]() (ChimerDB 3.0, 2016-12-01 and TCGA fusion Portal 2015-12-01) |
Database | Src | Cancer type | Sample | Fusion gene | ORF | 5'-gene BP | 3'-gene BP |
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TissGeneNet for HRASLS |
![]() (TCGA IlluminaHiSeq_RNASeqV2, pan-cancer normalized log2(norm_counts+1) data, version 2016-08-16) (PINA2 ppi data) |
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TissGeneProg for HRASLS |
![]() (TCGA IlluminaHiSeq_RNASeqV2, pan-cancer normalized log2(norm_counts+1) data, version 2016-08-16) (TCGA clinicalMatrix, phenotype data, version 2016-04-27) * Click on the image to enlarge it in a new window. |
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![]() (TCGA IlluminaHiSeq_RNASeqV2, pan-cancer normalized log2(norm_counts+1) data, version 2016-08-16) (TCGA clinicalMatrix, phenotype data, version 2016-04-27) * Click on the image enlarge it in a new window. |
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![]() (TCGA IlluminaHiSeq_RNASeqV2, pan-cancer normalized log2(norm_counts+1) data, version 2016-08-16) (TCGA clinicalMatrix, phenotype data, version 2016-04-27) * Click on the image enlarge it in a new window. |
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![]() (TCGA IlluminaHiSeq_RNASeqV2, pan-cancer normalized log2(norm_counts+1) data, version 2016-08-16) (TCGA clinicalMatrix, phenotype data, version 2016-04-27) * Click on the image enlarge it in a new window. |
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TissGeneClin for HRASLS |
TissGeneDrug for HRASLS |
![]() (DrugBank Version 5.0.6, 2017-04-01) |
DrugBank ID | Drug name | Drug activity | Drug type | Drug status |
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TissGeneDisease for HRASLS |
![]() (DisGeNet, 2016-06-01) |
Disease ID | Disease name | # pubmeds | Source |
umls:C0003850 | Arteriosclerosis | 2 | BeFree |
umls:C0004153 | Atherosclerosis | 2 | BeFree |
umls:C0024623 | Malignant neoplasm of stomach | 2 | BeFree |
umls:C0037773 | Spastic Paraplegia, Hereditary | 2 | BeFree |
umls:C0374997 | Helicobacter pylori (H. pylori) infection in conditions classified elsewhere and of unspecified site | 2 | BeFree |
umls:C0376358 | Malignant neoplasm of prostate | 2 | BeFree |
umls:C0600139 | Prostate carcinoma | 2 | BeFree |
umls:C0010054 | Coronary Arteriosclerosis | 1 | BeFree |
umls:C0020445 | Hypercholesterolemia, Familial | 1 | BeFree |
umls:C0020538 | Hypertensive disease | 1 | BeFree |
umls:C0038354 | Stomach Diseases | 1 | BeFree |
umls:C2931822 | Nasopharyngeal carcinoma | 1 | BeFree |
umls:C3714756 | Intellectual Disability | 1 | BeFree |