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REC114 (REC114 meiotic recombination protein)

Identity

Alias_namesC15orf60
chromosome 15 open reading frame 60
Alias_symbol (synonym)LOC283677
FLJ27520
FLJ36860
FLJ44083
CT147
Other alias
HGNC (Hugo) REC114
LocusID (NCBI) 283677
Atlas_Id 72567
Location 15q24.1  [Link to chromosome band 15q24]
Location_base_pair Starts at 73735499 and ends at 73852353 bp from pter ( according to hg19-Feb_2009)

Note

Non-annotated gene. Preliminary data : if you are an author
who wish to write a full paper/card on this gene, go to  How to contribute

DNA/RNA

 


External links

Nomenclature
HGNC (Hugo)REC114   25065
Cards
Entrez_Gene (NCBI)REC114  283677  REC114 meiotic recombination protein
AliasesC15orf60; CT147
GeneCards (Weizmann)REC114
Ensembl hg19 (Hinxton)ENSG00000183324 [Gene_View]  chr15:73735499-73852353 [Contig_View]  REC114 [Vega]
Ensembl hg38 (Hinxton)ENSG00000183324 [Gene_View]  chr15:73735499-73852353 [Contig_View]  REC114 [Vega]
ICGC DataPortalENSG00000183324
TCGA cBioPortalREC114
AceView (NCBI)REC114
Genatlas (Paris)REC114
WikiGenes283677
SOURCE (Princeton)REC114
Genetics Home Reference (NIH)REC114
Genomic and cartography
GoldenPath hg19 (UCSC)REC114  -     chr15:73735499-73852353 +  15q24.1   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)REC114  -     15q24.1   [Description]    (hg38-Dec_2013)
EnsemblREC114 - 15q24.1 [CytoView hg19]  REC114 - 15q24.1 [CytoView hg38]
Mapping of homologs : NCBIREC114 [Mapview hg19]  REC114 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AK131030 BC055412 BX113903 DB465854
RefSeq transcript (Entrez)NM_001042367
RefSeq genomic (Entrez)NC_000015 NC_018926 NT_010194 NW_004929398
Consensus coding sequences : CCDS (NCBI)REC114
Cluster EST : UnigeneHs.743574 [ NCBI ]
CGAP (NCI)Hs.743574
Alternative Splicing GalleryENSG00000183324
Gene ExpressionREC114 [ NCBI-GEO ]   REC114 [ EBI - ARRAY_EXPRESS ]   REC114 [ SEEK ]   REC114 [ MEM ]
Gene Expression Viewer (FireBrowse)REC114 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)283677
GTEX Portal (Tissue expression)REC114
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ7Z4M0   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ7Z4M0  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ7Z4M0
Splice isoforms : SwissVarQ7Z4M0
PhosPhoSitePlusQ7Z4M0
Domains : Interpro (EBI)REC114L   
Domain families : Pfam (Sanger)REC114-like (PF15165)   
Domain families : Pfam (NCBI)pfam15165   
Conserved Domain (NCBI)REC114
DMDM Disease mutations283677
Blocks (Seattle)REC114
SuperfamilyQ7Z4M0
Human Protein AtlasENSG00000183324
Peptide AtlasQ7Z4M0
IPIIPI00176901   
Protein Interaction databases
DIP (DOE-UCLA)Q7Z4M0
IntAct (EBI)Q7Z4M0
FunCoupENSG00000183324
BioGRIDREC114
STRING (EMBL)REC114
ZODIACREC114
Ontologies - Pathways
QuickGOQ7Z4M0
Ontology : AmiGODNA recombination  meiotic cell cycle  
Ontology : EGO-EBIDNA recombination  meiotic cell cycle  
NDEx NetworkREC114
Atlas of Cancer Signalling NetworkREC114
Wikipedia pathwaysREC114
Orthology - Evolution
OrthoDB283677
GeneTree (enSembl)ENSG00000183324
Phylogenetic Trees/Animal Genes : TreeFamREC114
HOVERGENQ7Z4M0
HOGENOMQ7Z4M0
Homologs : HomoloGeneREC114
Homology/Alignments : Family Browser (UCSC)REC114
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerREC114 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)REC114
dbVarREC114
ClinVarREC114
1000_GenomesREC114 
Exome Variant ServerREC114
ExAC (Exome Aggregation Consortium)REC114 (select the gene name)
Genetic variants : HAPMAP283677
Genomic Variants (DGV)REC114 [DGVbeta]
DECIPHER (Syndromes)15:73735499-73852353  ENSG00000183324
CONAN: Copy Number AnalysisREC114 
Mutations
ICGC Data PortalREC114 
TCGA Data PortalREC114 
Broad Tumor PortalREC114
OASIS PortalREC114 [ Somatic mutations - Copy number]
Mutations and Diseases : HGMDREC114
BioMutasearch REC114
DgiDB (Drug Gene Interaction Database)REC114
DoCM (Curated mutations)REC114 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)REC114 (select a term)
intoGenREC114
Cancer3DREC114(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenREC114
Genetic Testing Registry REC114
NextProtQ7Z4M0 [Medical]
TSGene283677
GENETestsREC114
Huge Navigator REC114 [HugePedia]
snp3D : Map Gene to Disease283677
BioCentury BCIQREC114
ClinGenREC114
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD283677
Chemical/Pharm GKB GenePA162378269
Clinical trialREC114
Miscellaneous
canSAR (ICR)REC114 (select the gene name)
Probes
Litterature
PubMed4 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineREC114
EVEXREC114
GoPubMedREC114
iHOPREC114
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Tue Mar 14 12:40:50 CET 2017

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