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FAM183CP (family with sequence similarity 183, member C, pseudogene)

Identity

Alias_namesfamily with sequence similarity 183, member C, pseudogene
Other alias-
HGNC (Hugo) FAM183CP
LocusID (NCBI) 286135
Atlas_Id 63090
Location 8p12  [Link to chromosome band 8p12]
Location_base_pair Starts at 29779029 and ends at 29811123 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)FAM183CP   27827
Cards
Entrez_Gene (NCBI)FAM183CP  286135  family with sequence similarity 183, member C, pseudogene
Aliases
GeneCards (Weizmann)FAM183CP
Ensembl hg19 (Hinxton)ENSG00000253279 [Gene_View]  chr8:29779029-29811123 [Contig_View]  FAM183CP [Vega]
Ensembl hg38 (Hinxton)ENSG00000253279 [Gene_View]  chr8:29779029-29811123 [Contig_View]  FAM183CP [Vega]
ICGC DataPortalENSG00000253279
TCGA cBioPortalFAM183CP
AceView (NCBI)FAM183CP
Genatlas (Paris)FAM183CP
WikiGenes286135
SOURCE (Princeton)FAM183CP
Genetics Home Reference (NIH)FAM183CP
Genomic and cartography
GoldenPath hg19 (UCSC)FAM183CP  -     chr8:29779029-29811123 +  8p12   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)FAM183CP  -     8p12   [Description]    (hg38-Dec_2013)
EnsemblFAM183CP - 8p12 [CytoView hg19]  FAM183CP - 8p12 [CytoView hg38]
Mapping of homologs : NCBIFAM183CP [Mapview hg19]  FAM183CP [Mapview hg38]
Gene and transcription
Genbank (Entrez)AL833525 BC028745 BC045833 BC126344 HG501023
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)NC_000008 NC_018919 NT_167187 NW_004929337
Consensus coding sequences : CCDS (NCBI)FAM183CP
Cluster EST : UnigeneHs.376840 [ NCBI ]
CGAP (NCI)Hs.376840
Alternative Splicing GalleryENSG00000253279
Gene ExpressionFAM183CP [ NCBI-GEO ]   FAM183CP [ EBI - ARRAY_EXPRESS ]   FAM183CP [ SEEK ]   FAM183CP [ MEM ]
Gene Expression Viewer (FireBrowse)FAM183CP [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)286135
GTEX Portal (Tissue expression)FAM183CP
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)FAM183CP
DMDM Disease mutations286135
Blocks (Seattle)FAM183CP
Human Protein AtlasENSG00000253279
IPIIPI00884039   
Protein Interaction databases
FunCoupENSG00000253279
BioGRIDFAM183CP
STRING (EMBL)FAM183CP
ZODIACFAM183CP
Ontologies - Pathways
Huge Navigator FAM183CP [HugePedia]
snp3D : Map Gene to Disease286135
BioCentury BCIQFAM183CP
ClinGenFAM183CP
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD286135
Clinical trialFAM183CP
Miscellaneous
canSAR (ICR)FAM183CP (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineFAM183CP
EVEXFAM183CP
GoPubMedFAM183CP
iHOPFAM183CP
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

Search in all EBI   NCBI

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indexed on : Tue Mar 14 12:03:44 CET 2017

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