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Bioinformatics and Systems Medicine Laboratory Bioinformatics and Systems Medicine Laboratory

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TissGeneSummary

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TissGeneExp

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TissGene-miRNA

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TissGeneMut: TissGeneSNV, TissGeneCNV, and TissGeneFusions

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TissGeneNet

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TissGeneProg

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TissGeneClin: TissGeneDrug and TissGeneDisease

TissGeneSummary for SDS
check button Gene summary
Basic gene informationGene symbolSDS
Gene nameserine dehydratase
SynonymsSDH
CytomapUCSC genome browser: 12q24.13
Type of geneprotein-coding
RefGenesNM_006843.2,
DescriptionL-serine ammonia-lyaseL-serine deaminaseL-serine dehydrataseL-serine dehydratase/L-threonine deaminaseL-threonine dehydrataseTDH
Modification date20141207
dbXrefs MIM : 182128
HGNC : HGNC
Ensembl : ENSG00000135094
HPRD : 01633
Vega : OTTHUMG00000169554
ProteinUniProt:
go to UniProt's Cross Reference DB Table
ExpressionCleanEX: HS_SDS
BioGPS: 10993
PathwayNCI Pathway Interaction Database: SDS
KEGG: SDS
REACTOME: SDS
Pathway Commons: SDS
ContextiHOP: SDS
ligand binding site mutation search in PubMed: SDS
UCL Cancer Institute: SDS
Assigned class in TissGDB*A
Included tissue-specific gene expression resourcesHPA,TiGER,GTEx
Specific-tissues in normal samples (assigned by TissGDB using HPA, TiGER, and GTEx)Liver
Cancer types related to the specific-tissues in cancer samples (assigned by TissGDB using TCGA)LIHC
Reference showing the relevant tissue of SDSSubcellular distribution of superoxide dismutases (SOD) in rat liver: Cu,Zn-SOD in mitochondria. Okado-Matsumoto A, Fridovich I. J Biol Chem. 2001 Oct 19;276(42):38388-93. Epub 2001 Aug 15 (pmid:11507097)
go to article
Description by TissGene annotations
* 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.

check button Gene ontology having evidence of Inferred from Direct Assay (IDA) from Entrez
GO IDGO termPubMed ID
GO:0006565L-serine catabolic process15689518
GO:0042866pyruvate biosynthetic process15689518
GO:0006565L-serine catabolic process15689518
GO:0042866pyruvate biosynthetic process15689518


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TissGeneExp for SDS

check button Gene expressions across 28 cancer types (X-axis: cancer type and Y-axis: log2(norm_counts+1))
(TCGA IlluminaHiSeq_RNASeqV2, pan-cancer normalized log2(norm_counts+1) data, version 2016-08-16)
gene exp


check button Gene isoform expressions across 28 cancer types (X-axis: cancer type and Y-axis: log2(norm_counts+1))
(TCGA pan-cancer tcga_rsem_isoform_tpm, version 2016-09-01)
gene isoform exp


check button Gene expressions across normal tissues of GTEx data
(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.
normal gene exp


check button Different expressions across 14 cancer types with more than 10 samples between matched tumors and normals (X-axis: cancer type and Y-axis: log2(norm_counts+1))
(TCGA IlluminaHiSeq_RNASeqV2, pan-cancer normalized log2(norm_counts+1) data, version 2016-08-16)
DEG exp

- Significantly differentially expressed cancer types and information. (|Fold change|>1 and FDR<0.05)
Cancer typeMean(exp) in tumorMean(exp) in matched normalLog2FCP-val.FDR
KIRP0.569924762-4.4713502385.0412751.17E-196.90E-18
BRCA0.091671198-2.6749972232.7666684212.20E-344.00E-33
STAD0.406609137-3.2211002383.6277093752.26E-113.63E-09
KIRC0.109503581-4.7312283634.8407319446.55E-402.67E-38
PRAD-1.824022594-3.3156899021.4916673081.81E-061.22E-05
KICH-0.559415363-4.4361793633.8767641.99E-091.18E-08
LIHC3.6305206376.729160637-3.098641.57E-071.05E-06
ESCA-0.621312454-3.8903579093.2690454550.0001670.0046982
LUAD-0.465294743-1.5311326741.0658379310.0006110.00137736
HNSC-0.787814991-2.6510289451.8632139531.95E-050.000103479


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TissGene-miRNA for SDS

check button Significantly anti-correlated miRNAs of TissGene across 28 cancer types
(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 typemiRNA idmiRNA accessionP-val.Coeff.# samples


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TissGeneMut for SDS
TissGeneSNV for SDS

check button nsSNV counts per each loci.
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.
SNV lollipop
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check button Somatic nucleotide variants of TissGene across 28 cancer types
(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)
SNV distribution

- nsSNVs sorted by frequency.
AAchangeCancer type# samples
p.K215*LUAD1
p.G161RSKCM1
p.I163TLIHC1
p.G161ESKCM1
p.G56DUCEC1
p.V149MTHCA1
p.W185*SKCM1
p.G170RSTAD1
p.I42VSARC1
p.A162GSTAD1
p.H59YESCA1
p.A104VCOAD1
p.A207TCOAD1
p.A253DLUAD1
p.I141MCESC1
p.A83TLGG1
p.K41NBLCA1
p.A253VESCA1
p.P88SPRAD1
p.P128LACC1
p.D138YHNSC1
p.A311TSTAD1
p.K100QLUAD1
p.E288KBLCA1
p.D261NLUAD1
p.R314PLUSC1
p.P128TACC1
p.K10NLUSC1


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TissGeneCNV for SDS

check button Copy number variations of TissGene across 28 cancer types (X-axis: cancer type and Y-axis: % of CNV samples)
(TCGA Gistic2_CopyNumber_Gistic2_all_data_by_genes, Gistic2 copy number data, version 2016-08-16)
CNV


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TissGeneFusions for SDS

check button Fusion genes including TissGene
(ChimerDB 3.0, 2016-12-01 and TCGA fusion Portal 2015-12-01)
DatabaseSrcCancer typeSampleFusion geneORF5'-gene BP3'-gene BP
Chimerdb3.0ChiTaRsNAAV645432SDS-GNA14chr12:113830890chr9:80136639
TCGAfusionPortalPRADAGBMTCGA-06-0129-01ANOC4L-SDSCDS-5UTRChr12:132629150Chr12:113837515


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TissGeneNet for SDS

check button Co-expressed gene networks based on protein-protein interaction data (CePIN)
(TCGA IlluminaHiSeq_RNASeqV2, pan-cancer normalized log2(norm_counts+1) data, version 2016-08-16)
(PINA2 ppi data)


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TissGeneProg for SDS

check button Kaplan-Meier plots with logrank tests of overall survival (OS) using 28 cancer types
(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.
survival 1

check button Kaplan-Meier plots with logrank test of relapse free survival (RFS) using 28 cancer types
(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.
survival 2

check button Forest plot of Cox proportional hazard ratio (HR) and 95% CI of overall survival (OS) using 28 cancer types
(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.
survival 3

check button Forest plot of Cox proportional hazard ratio (HR) and 95% CI of relapse free survival (RFS) using 28 cancer types
(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.
survival 4

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TissGeneClin for SDS
TissGeneDrug for SDS

check button Drug information targeting TissGene
(DrugBank Version 5.0.6, 2017-04-01)
DrugBank IDDrug nameDrug activityDrug typeDrug status


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TissGeneDisease for SDS

check button Disease information associated with TissGene
(DisGeNet, 2016-06-01)
Disease IDDisease name# pubmedsSource
umls:C0030421Paraganglioma40BeFree
umls:C0031511Pheochromocytoma22BeFree
umls:C0013336Dwarfism16BeFree
umls:C0028754Obesity10BeFree
umls:C0238198Gastrointestinal Stromal Tumors9BeFree
umls:C1333944Paragangliomas, head and neck6BeFree
umls:C0032002Pituitary Diseases5BeFree
umls:C0037889Hereditary spherocytosis5BeFree
umls:C0497406Overweight5BeFree
umls:C2674218SPHEROCYTOSIS, TYPE 1 (disorder)5BeFree
umls:C0007134Renal Cell Carcinoma4BeFree
umls:C0011854Diabetes Mellitus, Insulin-Dependent4BeFree
umls:C0015544Failure to Thrive4BeFree
umls:C1333993Hereditary Paraganglioma4BeFree
umls:C0003873Rheumatoid Arthritis3BeFree
umls:C0007570Celiac Disease3BeFree
umls:C0010674Cystic Fibrosis3BeFree
umls:C0011884Diabetic Retinopathy3BeFree,GAD
umls:C0013338Pituitary dwarfism3BeFree
umls:C0025202melanoma3BeFree
umls:C0041408Turner Syndrome3BeFree
umls:C0272170Shwachman syndrome3BeFree
umls:C0878787Growth failure3BeFree
umls:C0007102Malignant tumor of colon2BeFree
umls:C0011860Diabetes Mellitus, Non-Insulin-Dependent2BeFree,GAD
umls:C0011991Diarrhea2BeFree
umls:C0013902Elliptocytosis, Hereditary2BeFree
umls:C0015230Exanthema2BeFree
umls:C0018553Hamartoma Syndrome, Multiple2BeFree
umls:C0019562Von Hippel-Lindau Syndrome2BeFree
umls:C0020538Hypertensive disease2BeFree
umls:C0021400Influenza2BeFree
umls:C0022665Kidney Neoplasm2BeFree
umls:C0026764Multiple Myeloma2BeFree
umls:C0026837Muscle Rigidity2BeFree
umls:C0036421Systemic Scleroderma2BeFree
umls:C0042974von Willebrand Disease2BeFree
umls:C0271561Somatotropin deficiency2BeFree
umls:C0271568Laron Syndrome2BeFree
umls:C0282666Very Low Birth Weight2BeFree
umls:C0596263Carcinogenesis2BeFree
umls:C0699790Colon Carcinoma2BeFree
umls:C0740457Malignant neoplasm of kidney2BeFree
umls:C0751651Mitochondrial Diseases2BeFree
umls:C0848332Spots on skin2BeFree
umls:C1257877Pheochromocytoma, Extra-Adrenal2BeFree
umls:C1333768Gastric Gastrointestinal Stromal Tumor2BeFree
umls:C1855008Mitochondrial Complex II Deficiency2BeFree
umls:C1956346Coronary Artery Disease2BeFree
umls:C3714796Isolated somatotropin deficiency2BeFree
umls:C0001418Adenocarcinoma1BeFree
umls:C0002395Alzheimer's Disease1BeFree
umls:C0003872Arthritis, Psoriatic1BeFree
umls:C0004364Autoimmune Diseases1BeFree
umls:C0005684Malignant neoplasm of urinary bladder1BeFree
umls:C0007137Squamous cell carcinoma1BeFree
umls:C0007279Carotid Body Paraganglioma1BeFree
umls:C0007847Malignant tumor of cervix1BeFree
umls:C0007894Cestode Infections1BeFree
umls:C0008626Congenital chromosomal disease1BeFree
umls:C0009663Condylomata Acuminata1BeFree
umls:C0011570Mental Depression1BeFree
umls:C0011581Depressive disorder1BeFree
umls:C0011644Scleroderma1BeFree
umls:C0014038Encephalitis1BeFree
umls:C0020456Hyperglycemia1BeFree
umls:C0021670insulinoma1BeFree
umls:C0023267Fibroid Tumor1BeFree
umls:C0023364Leptospirosis1BeFree
umls:C0023434Chronic Lymphocytic Leukemia1BeFree
umls:C0023467Leukemia, Myelocytic, Acute1BeFree
umls:C0024141Lupus Erythematosus, Systemic1BeFree
umls:C0024299Lymphoma1BeFree
umls:C0027627Neoplasm Metastasis1BeFree
umls:C0027662Multiple Endocrine Neoplasia1BeFree
umls:C0027831Neurofibromatosis 11BeFree
umls:C0030422Extra-Adrenal Paraganglioma1BeFree
umls:C0030805Bullous pemphigoid1BeFree
umls:C0031212Personality Disorders1BeFree
umls:C0032000Pituitary Adenoma1BeFree
umls:C0036341Schizophrenia1BeFree
umls:C0039984Thoracic Outlet Syndrome1BeFree
umls:C0040015Thrombasthenia1BeFree
umls:C0042133Uterine Fibroids1BeFree
umls:C0042755Virilism1BeFree
umls:C0085400Neurofibrillary degeneration (morphologic abnormality)1BeFree
umls:C0086132Depressive Symptoms1BeFree
umls:C0154830Proliferative diabetic retinopathy1BeFree
umls:C0175693Russell-Silver syndrome1BeFree
umls:C0206157Myopathies, Nemaline1BeFree
umls:C0221155Systolic hypertension1BeFree
umls:C0235222Diastolic hypertension1BeFree
umls:C0235946Cerebral atrophy1BeFree
umls:C0268164Primary hyperoxaluria, type I1BeFree
umls:C0270612Leukoencephalopathies1BeFree
umls:C0282577Congenital Disorders of Glycosylation1BeFree
umls:C0302592Cervix carcinoma1BeFree
umls:C0333463Senile Plaques1BeFree
umls:C0342538Constitutional delay of growth and puberty1BeFree
umls:C0376358Malignant neoplasm of prostate1BeFree
umls:C0424790Rigor - Temperature-associated observation1BeFree
umls:C0524851Neurodegenerative Disorders1BeFree
umls:C0600139Prostate carcinoma1BeFree
umls:C0699885Carcinoma of bladder1BeFree
umls:C0729233Dissecting aneurysm of the thoracic aorta1BeFree
umls:C0747102Ovarian failure1BeFree
umls:C0878544Cardiomyopathies1BeFree
umls:C1263846Attention deficit hyperactivity disorder1BeFree
umls:C1334699Mesenchymal Cell Neoplasm1BeFree
umls:C1378703Renal carcinoma1BeFree
umls:C1559093Bruising in the Absence of Grade 3 or Grade 4 Thrombocytopenia Adverse Event1BeFree
umls:C1832588Chromosome 11p11.2 Deletion Syndrome1BeFree
umls:C1849193PEELING SKIN SYNDROME1BeFree
umls:C1854520SEBASTIAN SYNDROME1BeFree
umls:C1858592Carney Triad1BeFree
umls:C2936349Plaque, Amyloid1BeFree
umls:C2986691Inherited bone marrow failure syndrome1BeFree