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Phenotypic Information (metabolism pathway, cancer, disease, phenome) | |
Gene-Gene Network Information: Co-Expression Network, Interacting Genes & KEGG | |
Gene Summary for SRR |
Basic gene info. | Gene symbol | SRR |
Gene name | serine racemase | |
Synonyms | ILV1|ISO1 | |
Cytomap | UCSC genome browser: 17p13 | |
Genomic location | chr17 :2207247-2228553 | |
Type of gene | protein-coding | |
RefGenes | NM_021947.1, | |
Ensembl id | ENSG00000167720 | |
Description | D-serine ammonia-lyaseD-serine dehydrataseL-serine ammonia-lyaseL-serine dehydratase | |
Modification date | 20141207 | |
dbXrefs | MIM : 606477 | |
HGNC : HGNC | ||
Ensembl : ENSG00000167720 | ||
HPRD : 10451 | ||
Vega : OTTHUMG00000090583 | ||
Protein | UniProt: go to UniProt's Cross Reference DB Table | |
Expression | CleanEX: HS_SRR | |
BioGPS: 63826 | ||
Gene Expression Atlas: ENSG00000167720 | ||
The Human Protein Atlas: ENSG00000167720 | ||
Pathway | NCI Pathway Interaction Database: SRR | |
KEGG: SRR | ||
REACTOME: SRR | ||
ConsensusPathDB | ||
Pathway Commons: SRR | ||
Metabolism | MetaCyc: SRR | |
HUMANCyc: SRR | ||
Regulation | Ensembl's Regulation: ENSG00000167720 | |
miRBase: chr17 :2,207,247-2,228,553 | ||
TargetScan: NM_021947 | ||
cisRED: ENSG00000167720 | ||
Context | iHOP: SRR | |
cancer metabolism search in PubMed: SRR | ||
UCL Cancer Institute: SRR | ||
Assigned class in ccmGDB | C |
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Phenotypic Information for SRR(metabolism pathway, cancer, disease, phenome) |
Cancer Description | |
Cancer | CGAP: SRR |
Familial Cancer Database: SRR |
* This gene is included in those cancer gene databases. |
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Oncogene 1 | Significant driver gene in |
cf) number; DB name 1 Oncogene; http://nar.oxfordjournals.org/content/35/suppl_1/D721.long, 2 Tumor Suppressor gene; https://bioinfo.uth.edu/TSGene/, 3 Cancer Gene Census; http://www.nature.com/nrc/journal/v4/n3/abs/nrc1299.html, 4 CancerGenes; http://nar.oxfordjournals.org/content/35/suppl_1/D721.long, 5 Network of Cancer Gene; http://ncg.kcl.ac.uk/index.php, 1Therapeutic Vulnerabilities in Cancer; http://cbio.mskcc.org/cancergenomics/statius/ |
Metabolic Pathway Description | |
KEGG_GLYCINE_SERINE_AND_THREONINE_METABOLISM |
Others | |
OMIM | |
Orphanet | |
Disease | KEGG Disease: SRR |
MedGen: SRR (Human Medical Genetics with Condition) | |
ClinVar: SRR | |
Phenotype | MGI: SRR (International Mouse Phenotyping Consortium) |
PhenomicDB: SRR |
Mutations for SRR |
* Under tables are showing count per each tissue to give us broad intuition about tissue specific mutation patterns.You can go to the detailed page for each mutation database's web site. |
Structural Variants in COSMIC: go to COSMIC mutation histogram |
- Statistics for Tissue and Mutation type | Top |
- For Inter-chromosomal Variations |
* Inter-chromosomal variantions includes 'interchromosomal amplicon to amplicon', 'interchromosomal amplicon to non-amplified dna', 'interchromosomal insertion', 'Interchromosomal unknown type'. |
- For Intra-chromosomal Variations |
* Intra-chromosomal variantions includes 'intrachromosomal amplicon to amplicon', 'intrachromosomal amplicon to non-amplified dna', 'intrachromosomal deletion', 'intrachromosomal fold-back inversion', 'intrachromosomal inversion', 'intrachromosomal tandem duplication', 'Intrachromosomal unknown type', 'intrachromosomal with inverted orientation', 'intrachromosomal with non-inverted orientation'. |
Sample | Symbol_a | Chr_a | Start_a | End_a | Symbol_b | Chr_b | Start_b | End_b |
ovary | SRR | chr17 | 2219606 | 2219626 | SMG6 | chr17 | 2130138 | 2130158 |
pancreas | SRR | chr17 | 2209364 | 2209384 | SRR | chr17 | 2211109 | 2211129 |
pancreas | SRR | chr17 | 2214790 | 2214810 | chr14 | 22043829 | 22043849 |
cf) Tissue number; Tissue name (1;Breast, 2;Central_nervous_system, 3;Haematopoietic_and_lymphoid_tissue, 4;Large_intestine, 5;Liver, 6;Lung, 7;Ovary, 8;Pancreas, 9;Prostate, 10;Skin, 11;Soft_tissue, 12;Upper_aerodigestive_tract) |
Related fusion transcripts : go to Chitars2.0 |
* From mRNA Sanger sequences, Chitars2.0 arranged chimeric transcripts. This table shows SRR related fusion information. |
ID | Head Gene | Tail Gene | Accession | Gene_a | qStart_a | qEnd_a | Chromosome_a | tStart_a | tEnd_a | Gene_a | qStart_a | qEnd_a | Chromosome_a | tStart_a | tEnd_a |
CN347172 | SRR | 1 | 541 | 17 | 2226860 | 2227400 | ROMO1 | 539 | 601 | 20 | 34288835 | 34288897 | |
AA614279 | FUS | 1 | 323 | 16 | 31202314 | 31202923 | SRR | 319 | 376 | 17 | 2208426 | 2208483 |
Other DBs for Structural Variants |
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Copy Number Variations in COSMIC: go to COSMIC mutation CNV/Expr |
There's no copy number variation information in COSMIC data for this gene. |
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SNV Counts per Each Loci in COSMIC data: go to COSMIC point mutation |
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Somatic Mutation Counts per Tissue in COSMIC data |
Stat. for Non-Synonymous SNVs (# total SNVs=19) | (# total SNVs=4) |
(# total SNVs=1) | (# total SNVs=0) |
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Top 10 SNVs Having the Most Samples in COSMIC data |
* When you move the cursor on each content, you can see more deailed mutation information on the Tooltip. Those are primary_site,primary_histology,mutation(aa),pubmedID. |
GRCh37 position | Mutation(aa) | Unique sampleID count |
chr17:2221171-2221171 | p.G59D | 3 |
chr17:2218973-2218973 | p.R40H | 2 |
chr17:2227019-2227019 | p.A292G | 2 |
chr17:2224624-2224624 | p.V142I | 1 |
chr17:2227020-2227020 | p.A292A | 1 |
chr17:2221250-2221250 | p.G85G | 1 |
chr17:2224685-2224685 | p.G162A | 1 |
chr17:2227116-2227117 | p.W325fs*5 | 1 |
chr17:2221269-2221269 | p.T92P | 1 |
chr17:2224836-2224836 | p.V174F | 1 |
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SNV Counts per Each Loci in TCGA data |
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Point Mutation/ Tissue ID | 1 | 2 | 3 | 4 | 5 | 6 | 7 | 8 | 9 | 10 | 11 | 12 | 13 | 14 | 15 | 16 | 17 | 18 | 19 | 20 |
# sample | 3 |   |   | 3 |   |   |   |   |   |   |   | 1 | 1 | 1 |   |   |   | 4 | 1 | 4 |
# mutation | 3 |   |   | 3 |   |   |   |   |   |   |   | 1 | 1 | 1 |   |   |   | 4 | 1 | 5 |
nonsynonymous SNV | 2 |   |   | 3 |   |   |   |   |   |   |   | 1 |   | 1 |   |   |   | 4 | 1 | 4 |
synonymous SNV | 1 |   |   |   |   |   |   |   |   |   |   |   | 1 |   |   |   |   |   |   | 1 |
cf) Tissue ID; Tissue type (1; BLCA[Bladder Urothelial Carcinoma], 2; BRCA[Breast invasive carcinoma], 3; CESC[Cervical squamous cell carcinoma and endocervical adenocarcinoma], 4; COAD[Colon adenocarcinoma], 5; GBM[Glioblastoma multiforme], 6; Glioma Low Grade, 7; HNSC[Head and Neck squamous cell carcinoma], 8; KICH[Kidney Chromophobe], 9; KIRC[Kidney renal clear cell carcinoma], 10; KIRP[Kidney renal papillary cell carcinoma], 11; LAML[Acute Myeloid Leukemia], 12; LUAD[Lung adenocarcinoma], 13; LUSC[Lung squamous cell carcinoma], 14; OV[Ovarian serous cystadenocarcinoma ], 15; PAAD[Pancreatic adenocarcinoma], 16; PRAD[Prostate adenocarcinoma], 17; SKCM[Skin Cutaneous Melanoma], 18:STAD[Stomach adenocarcinoma], 19:THCA[Thyroid carcinoma], 20:UCEC[Uterine Corpus Endometrial Carcinoma]) |
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Top 10 SNVs Having the Most Samples in TCGA data |
* We represented just top 10 SNVs. When you move the cursor on each content, you can see more deailed mutation information on the Tooltip. Those are primary_site, primary_histology, mutation(aa), pubmedID. |
Genomic Position | Mutation(aa) | Unique sampleID count |
chr17:2218973 | p.R40H | 2 |
chr17:2221250 | p.A117G | 1 |
chr17:2226491 | p.Y127Y | 1 |
chr17:2222127 | p.P130S | 1 |
chr17:2226566 | p.V142I | 1 |
chr17:2222158 | p.P153P | 1 |
chr17:2226989 | p.G162A | 1 |
chr17:2222174 | p.G164R | 1 |
chr17:2227145 | p.V174F | 1 |
chr17:2222205 | p.Q219L | 1 |
Other DBs for Point Mutations |
Copy Number for SRR in TCGA |
* Copy number data were extracted from TCGA using R package TCGA-Assembler. The URLs of all public data files on TCGA DCC data server were gathered on Jan-05-2015. Function ProcessCNAData in TCGA-Assembler package was used to obtain gene-level copy number value which is calculated as the average copy number of the genomic region of a gene. |
cf) Tissue ID[Tissue type]: BLCA[Bladder Urothelial Carcinoma], BRCA[Breast invasive carcinoma], CESC[Cervical squamous cell carcinoma and endocervical adenocarcinoma], COAD[Colon adenocarcinoma], GBM[Glioblastoma multiforme], Glioma Low Grade, HNSC[Head and Neck squamous cell carcinoma], KICH[Kidney Chromophobe], KIRC[Kidney renal clear cell carcinoma], KIRP[Kidney renal papillary cell carcinoma], LAML[Acute Myeloid Leukemia], LUAD[Lung adenocarcinoma], LUSC[Lung squamous cell carcinoma], OV[Ovarian serous cystadenocarcinoma ], PAAD[Pancreatic adenocarcinoma], PRAD[Prostate adenocarcinoma], SKCM[Skin Cutaneous Melanoma], STAD[Stomach adenocarcinoma], THCA[Thyroid carcinoma], UCEC[Uterine Corpus Endometrial Carcinoma] |
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Gene Expression for SRR |
Gene Expression in Cancer Cell-lines (CCLE) |
* CCLE gene expression data were extracted from CCLE_Expression_Entrez_2012-10-18.res: Gene-centric RMA-normalized mRNA expression data. |
Differential Gene Expression in Primary Tumors (TCGA) |
* Normalized gene expression data of RNASeqV2 was extracted from TCGA using R package TCGA-Assembler. The URLs of all public data files on TCGA DCC data server were gathered at Jan-05-2015. Only eight cancer types have enough normal control samples for differential expression analysis. (t test, adjusted p<0.05 (using Benjamini-Hochberg FDR)) |
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CNV vs Gene Expression Plot |
* This plots show the correlation between CNV and gene expression. |
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Gene-Gene Network Information |
Co-Expressed gene's network Plot |
* Co-Expression network figures were drawn using R package igraph. Only the top 20 genes with the highest correlations were shown. Red circle: input gene, orange circle: cell metabolism gene, sky circle: other gene |
C17orf97,CYB5D1,CYB5D2,GLOD4,KIAA0753,LRRC48,MAP2K4, MED31,METTL16,PIGV,PNPLA4,RABEP1,RBKS,RNF167, SMG6,SRR,TMEM107,TTC19,YWHAE,ZBTB4,ZNF18 | BLZF1,URI1,TRAPPC13,CPD,DHX29,ERGIC2,GOLGA5, ITFG1,JKAMP,MAP4K3,PIGB,PLA2G12A,RAB5A,RCN2, RNF141,RNF14,SCARB2,SRR,UBA5,UBE2K,UEVLD | ||||
ATPAF2,C17orf49,C17orf85,COPS3,DERL2,EIF4A1,GLOD4, MED11,MIS12,OVCA2,PEMT,RNF167,RNMTL1,RPA1, SLC25A11,SRR,STX8,TIMM22,TXNL1,UBE2G1,YWHAE | ARL3,FAM229B,CFAP36,COX7A1,CUEDC2,EIF5A2,FAM195B, KCNMB2,KIAA0895,MSANTD4,KPNA5,LAYN,NKIRAS1,NME4, NME5,SNRPN,SRR,TCEAL1,TCEAL7,TCEAL8,TMEM17 |
Co-Expressed gene's Protein-protein interaction Network Plot |
* Co-Expression network figures were drawn using R package igraph. Only the top 20 genes with the highest correlations were shown. Red circle: input gene, orange circle: cell metabolism gene, sky circle: other gene |
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Interacting Genes (from Pathway Commons) |
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Pharmacological Information for SRR |
Cross-referenced pharmacological DB IDs from Uniprot |
DB Category | DB Name | DB's ID and Url link |
Drug-Gene Interaction Network |
* Gene Centered Interaction Network. |
* Drug Centered Interaction Network. |
DrugBank ID | Target Name | Drug Groups | Generic Name | Drug Centered Network | Drug Structure |
DB00114 | serine racemase | nutraceutical | Pyridoxal Phosphate | ||
DB00133 | serine racemase | approved; nutraceutical | L-Serine |
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Cross referenced IDs for SRR |
* We obtained these cross-references from Uniprot database. It covers 150 different DBs, 18 categories. http://www.uniprot.org/help/cross_references_section |
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