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FAM185A (family with sequence similarity 185 member A)

Identity

Alias_namesfamily with sequence similarity 185, member A
Alias_symbol (synonym)MGC35361
Other alias-
HGNC (Hugo) FAM185A
LocusID (NCBI) 222234
Atlas_Id 63093
Location 7q22.1  [Link to chromosome band 7q22]
Location_base_pair Starts at 102748952 and ends at 102809225 bp from pter ( according to hg38-Dec_2013)

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)FAM185A   22412
Cards
Entrez_Gene (NCBI)FAM185A  222234  family with sequence similarity 185 member A
Aliases
GeneCards (Weizmann)FAM185A
Ensembl hg19 (Hinxton) [Gene_View]
Ensembl hg38 (Hinxton) [Gene_View]  chr7:102748952-102809225 [Contig_View]  FAM185A [Vega]
TCGA cBioPortalFAM185A
AceView (NCBI)FAM185A
Genatlas (Paris)FAM185A
WikiGenes222234
SOURCE (Princeton)FAM185A
Genetics Home Reference (NIH)FAM185A
Genomic and cartography
GoldenPath hg38 (UCSC)FAM185A  -     chr7:102748952-102809225 +  7q22.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)FAM185A  -     7q22.1   [Description]    (hg19-Feb_2009)
EnsemblFAM185A - 7q22.1 [CytoView hg19]  FAM185A - 7q22.1 [CytoView hg38]
Mapping of homologs : NCBIFAM185A [Mapview hg19]  FAM185A [Mapview hg38]
Gene and transcription
Genbank (Entrez)AK054745 AK297455 AK298753 BC029175 DB192367
RefSeq transcript (Entrez)NM_001145268 NM_001145269 NM_001350987 NM_147194
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)FAM185A
Cluster EST : UnigeneHs.202543 [ NCBI ]
CGAP (NCI)Hs.202543
Gene ExpressionFAM185A [ NCBI-GEO ]   FAM185A [ EBI - ARRAY_EXPRESS ]   FAM185A [ SEEK ]   FAM185A [ MEM ]
Gene Expression Viewer (FireBrowse)FAM185A [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)222234
GTEX Portal (Tissue expression)FAM185A
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ8N0U4   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ8N0U4  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ8N0U4
Splice isoforms : SwissVarQ8N0U4
PhosPhoSitePlusQ8N0U4
Domains : Interpro (EBI)DUF4097   
Domain families : Pfam (Sanger)DUF4097 (PF13349)   
Domain families : Pfam (NCBI)pfam13349   
Conserved Domain (NCBI)FAM185A
DMDM Disease mutations222234
Blocks (Seattle)FAM185A
SuperfamilyQ8N0U4
Peptide AtlasQ8N0U4
HPRD11343
IPIIPI00884910   IPI00871367   IPI00916414   IPI00909165   IPI00916108   IPI01011056   
Protein Interaction databases
DIP (DOE-UCLA)Q8N0U4
IntAct (EBI)Q8N0U4
BioGRIDFAM185A
STRING (EMBL)FAM185A
ZODIACFAM185A
Ontologies - Pathways
QuickGOQ8N0U4
Ontology : AmiGOcytosol  
Ontology : EGO-EBIcytosol  
NDEx NetworkFAM185A
Atlas of Cancer Signalling NetworkFAM185A
Wikipedia pathwaysFAM185A
Orthology - Evolution
OrthoDB222234
Phylogenetic Trees/Animal Genes : TreeFamFAM185A
HOVERGENQ8N0U4
HOGENOMQ8N0U4
Homologs : HomoloGeneFAM185A
Homology/Alignments : Family Browser (UCSC)FAM185A
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerFAM185A [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)FAM185A
dbVarFAM185A
ClinVarFAM185A
1000_GenomesFAM185A 
Exome Variant ServerFAM185A
ExAC (Exome Aggregation Consortium)FAM185A (select the gene name)
Genetic variants : HAPMAP222234
Genomic Variants (DGV)FAM185A [DGVbeta]
DECIPHERFAM185A [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisFAM185A 
Mutations
ICGC Data PortalFAM185A 
TCGA Data PortalFAM185A 
Broad Tumor PortalFAM185A
OASIS PortalFAM185A [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICFAM185A  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDFAM185A
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 FAM185A
DgiDB (Drug Gene Interaction Database)FAM185A
DoCM (Curated mutations)FAM185A (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)FAM185A (select a term)
intoGenFAM185A
Cancer3DFAM185A(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenFAM185A
Genetic Testing Registry FAM185A
NextProtQ8N0U4 [Medical]
TSGene222234
GENETestsFAM185A
Target ValidationFAM185A
Huge Navigator FAM185A [HugePedia]
snp3D : Map Gene to Disease222234
BioCentury BCIQFAM185A
ClinGenFAM185A
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD222234
Chemical/Pharm GKB GenePA164719851
Clinical trialFAM185A
Miscellaneous
canSAR (ICR)FAM185A (select the gene name)
Probes
Litterature
PubMed5 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineFAM185A
EVEXFAM185A
GoPubMedFAM185A
iHOPFAM185A
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Mon Sep 18 13:07:45 CEST 2017

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