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FAM236C (family with sequence similarity 236 member C)

Identity

Other aliasFAM236D
HGNC (Hugo) FAM236C
LocusID (NCBI) 109729126
Atlas_Id 80196
Location Xq13.1  [Link to chromosome band Xq13]
Location_base_pair Starts at 72807425 and ends at 72808210 bp from pter ( according to hg38-Dec_2013)
Fusion genes
(updated 2017)
Data from Atlas, Mitelman, Cosmic Fusion, Fusion Cancer, TCGA fusion databases with official HUGO symbols (see references in chromosomal bands)
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


External links

Nomenclature
HGNC (Hugo)FAM236C   52641
Cards
Entrez_Gene (NCBI)FAM236C  109729126  family with sequence similarity 236 member C
AliasesFAM236D
GeneCards (Weizmann)FAM236C
Ensembl hg19 (Hinxton)ENSG00000283594 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000283594 [Gene_View]  chrX:72807425-72808210 [Contig_View]  FAM236C [Vega]
ICGC DataPortalENSG00000283594
TCGA cBioPortalFAM236C
AceView (NCBI)FAM236C
Genatlas (Paris)FAM236C
WikiGenes109729126
SOURCE (Princeton)FAM236C
Genetics Home Reference (NIH)FAM236C
Genomic and cartography
GoldenPath hg38 (UCSC)FAM236C  -     chrX:72807425-72808210 -  Xq13.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)FAM236C  -     Xq13.1   [Description]    (hg19-Feb_2009)
EnsemblFAM236C - Xq13.1 [CytoView hg19]  FAM236C - Xq13.1 [CytoView hg38]
Mapping of homologs : NCBIFAM236C [Mapview hg19]  FAM236C [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)NM_001351111 NM_001351112
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)FAM236C
Alternative Splicing GalleryENSG00000283594
Gene ExpressionFAM236C [ NCBI-GEO ]   FAM236C [ EBI - ARRAY_EXPRESS ]   FAM236C [ SEEK ]   FAM236C [ MEM ]
Gene Expression Viewer (FireBrowse)FAM236C [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)109729126
GTEX Portal (Tissue expression)FAM236C
Human Protein AtlasENSG00000283594-FAM236C [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)FAM236C
DMDM Disease mutations109729126
Blocks (Seattle)FAM236C
Human Protein Atlas [tissue]ENSG00000283594-FAM236C [tissue]
Protein Interaction databases
FunCoupENSG00000283594
BioGRIDFAM236C
STRING (EMBL)FAM236C
ZODIACFAM236C
Ontologies - Pathways
Huge Navigator FAM236C [HugePedia]
snp3D : Map Gene to Disease109729126
BioCentury BCIQFAM236C
ClinGenFAM236C
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD109729126
Clinical trialFAM236C
Miscellaneous
canSAR (ICR)FAM236C (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineFAM236C
EVEXFAM236C
GoPubMedFAM236C
iHOPFAM236C
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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© Atlas of Genetics and Cytogenetics in Oncology and Haematology
indexed on : Tue Nov 21 13:59:32 CET 2017

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