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FAM181A (family with sequence similarity 181, member A)

Identity

Alias_namesC14orf152
chromosome 14 open reading frame 152
family with sequence similarity 181, member A
Other alias
HGNC (Hugo) FAM181A
LocusID (NCBI) 90050
Atlas_Id 63084
Location 14q32.12  [Link to chromosome band 14q32]
Location_base_pair Starts at 94385240 and ends at 94395954 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)FAM181A   20491
Cards
Entrez_Gene (NCBI)FAM181A  90050  family with sequence similarity 181, member A
AliasesC14orf152
GeneCards (Weizmann)FAM181A
Ensembl hg19 (Hinxton)ENSG00000140067 [Gene_View]  chr14:94385240-94395954 [Contig_View]  FAM181A [Vega]
Ensembl hg38 (Hinxton)ENSG00000140067 [Gene_View]  chr14:94385240-94395954 [Contig_View]  FAM181A [Vega]
ICGC DataPortalENSG00000140067
TCGA cBioPortalFAM181A
AceView (NCBI)FAM181A
Genatlas (Paris)FAM181A
WikiGenes90050
SOURCE (Princeton)FAM181A
Genetics Home Reference (NIH)FAM181A
Genomic and cartography
GoldenPath hg19 (UCSC)FAM181A  -     chr14:94385240-94395954 +  14q32.12   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)FAM181A  -     14q32.12   [Description]    (hg38-Dec_2013)
EnsemblFAM181A - 14q32.12 [CytoView hg19]  FAM181A - 14q32.12 [CytoView hg38]
Mapping of homologs : NCBIFAM181A [Mapview hg19]  FAM181A [Mapview hg38]
Gene and transcription
Genbank (Entrez)AK093387 AK315393 AY255795 BC009073 CX870424
RefSeq transcript (Entrez)NM_001207071 NM_001207072 NM_001207073 NM_001207074 NM_138344
RefSeq genomic (Entrez)NC_000014 NC_018925 NT_026437 NT_187601 NW_004929393
Consensus coding sequences : CCDS (NCBI)FAM181A
Cluster EST : UnigeneHs.525550 [ NCBI ]
CGAP (NCI)Hs.525550
Alternative Splicing GalleryENSG00000140067
Gene ExpressionFAM181A [ NCBI-GEO ]   FAM181A [ EBI - ARRAY_EXPRESS ]   FAM181A [ SEEK ]   FAM181A [ MEM ]
Gene Expression Viewer (FireBrowse)FAM181A [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)90050
GTEX Portal (Tissue expression)FAM181A
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ8N9Y4   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ8N9Y4  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ8N9Y4
Splice isoforms : SwissVarQ8N9Y4
PhosPhoSitePlusQ8N9Y4
Domains : Interpro (EBI)FAM181   
Domain families : Pfam (Sanger)FAM181 (PF15238)   
Domain families : Pfam (NCBI)pfam15238   
Conserved Domain (NCBI)FAM181A
DMDM Disease mutations90050
Blocks (Seattle)FAM181A
SuperfamilyQ8N9Y4
Human Protein AtlasENSG00000140067
Peptide AtlasQ8N9Y4
HPRD12636
IPIIPI00329828   IPI00607832   IPI01024898   IPI01026151   
Protein Interaction databases
DIP (DOE-UCLA)Q8N9Y4
IntAct (EBI)Q8N9Y4
FunCoupENSG00000140067
BioGRIDFAM181A
STRING (EMBL)FAM181A
ZODIACFAM181A
Ontologies - Pathways
QuickGOQ8N9Y4
Ontology : AmiGO
Ontology : EGO-EBI
NDEx NetworkFAM181A
Atlas of Cancer Signalling NetworkFAM181A
Wikipedia pathwaysFAM181A
Orthology - Evolution
OrthoDB90050
GeneTree (enSembl)ENSG00000140067
Phylogenetic Trees/Animal Genes : TreeFamFAM181A
HOVERGENQ8N9Y4
HOGENOMQ8N9Y4
Homologs : HomoloGeneFAM181A
Homology/Alignments : Family Browser (UCSC)FAM181A
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerFAM181A [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)FAM181A
dbVarFAM181A
ClinVarFAM181A
1000_GenomesFAM181A 
Exome Variant ServerFAM181A
ExAC (Exome Aggregation Consortium)FAM181A (select the gene name)
Genetic variants : HAPMAP90050
Genomic Variants (DGV)FAM181A [DGVbeta]
DECIPHER (Syndromes)14:94385240-94395954  ENSG00000140067
CONAN: Copy Number AnalysisFAM181A 
Mutations
ICGC Data PortalFAM181A 
TCGA Data PortalFAM181A 
Broad Tumor PortalFAM181A
OASIS PortalFAM181A [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICFAM181A  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDFAM181A
LOVD (Leiden Open Variation Database)Whole genome datasets
LOVD (Leiden Open Variation Database)LOVD - Leiden Open Variation Database
LOVD (Leiden Open Variation Database)LOVD 3.0 shared installation
BioMutasearch FAM181A
DgiDB (Drug Gene Interaction Database)FAM181A
DoCM (Curated mutations)FAM181A (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)FAM181A (select a term)
intoGenFAM181A
Cancer3DFAM181A(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenFAM181A
Genetic Testing Registry FAM181A
NextProtQ8N9Y4 [Medical]
TSGene90050
GENETestsFAM181A
Huge Navigator FAM181A [HugePedia]
snp3D : Map Gene to Disease90050
BioCentury BCIQFAM181A
ClinGenFAM181A
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD90050
Chemical/Pharm GKB GenePA162387582
Clinical trialFAM181A
Miscellaneous
canSAR (ICR)FAM181A (select the gene name)
Probes
Litterature
PubMed5 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineFAM181A
EVEXFAM181A
GoPubMedFAM181A
iHOPFAM181A
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 12:03:42 CET 2017

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