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FAM74A7 (family with sequence similarity 74 member A7)

Identity

Alias_namesfamily with sequence similarity 74, member A7, pseudogene
family with sequence similarity 74, member A7
Other alias-
HGNC (Hugo) FAM74A7
LocusID (NCBI) 100996582
Atlas_Id 77595
Location 9p11.2  [Link to chromosome band 9p11]
Location_base_pair Starts at 42198862 and ends at 42206016 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)FAM74A7   34037
Cards
Entrez_Gene (NCBI)FAM74A7  100996582  family with sequence similarity 74 member A7
Aliases
GeneCards (Weizmann)FAM74A7
Ensembl hg19 (Hinxton) [Gene_View]
Ensembl hg38 (Hinxton) [Gene_View]  chr9:42198862-42206016 [Contig_View]  FAM74A7 [Vega]
TCGA cBioPortalFAM74A7
AceView (NCBI)FAM74A7
Genatlas (Paris)FAM74A7
WikiGenes100996582
SOURCE (Princeton)FAM74A7
Genetics Home Reference (NIH)FAM74A7
Genomic and cartography
GoldenPath hg38 (UCSC)FAM74A7  -     chr9:42198862-42206016 +  9p11.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)FAM74A7  -     9p11.2   [Description]    (hg19-Feb_2009)
EnsemblFAM74A7 - 9p11.2 [CytoView hg19]  FAM74A7 - 9p11.2 [CytoView hg38]
Mapping of homologs : NCBIFAM74A7 [Mapview hg19]  FAM74A7 [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)FAM74A7
Gene ExpressionFAM74A7 [ NCBI-GEO ]   FAM74A7 [ EBI - ARRAY_EXPRESS ]   FAM74A7 [ SEEK ]   FAM74A7 [ MEM ]
Gene Expression Viewer (FireBrowse)FAM74A7 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)100996582
GTEX Portal (Tissue expression)FAM74A7
Protein : pattern, domain, 3D structure
UniProt/SwissProtA6NL05   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtA6NL05  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProA6NL05
Splice isoforms : SwissVarA6NL05
PhosPhoSitePlusA6NL05
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)FAM74A7
DMDM Disease mutations100996582
Blocks (Seattle)FAM74A7
SuperfamilyA6NL05
Peptide AtlasA6NL05
Protein Interaction databases
DIP (DOE-UCLA)A6NL05
IntAct (EBI)A6NL05
BioGRIDFAM74A7
STRING (EMBL)FAM74A7
ZODIACFAM74A7
Ontologies - Pathways
QuickGOA6NL05
Ontology : AmiGOintegral component of membrane  
Ontology : EGO-EBIintegral component of membrane  
NDEx NetworkFAM74A7
Atlas of Cancer Signalling NetworkFAM74A7
Wikipedia pathwaysFAM74A7
Orthology - Evolution
OrthoDB100996582
Phylogenetic Trees/Animal Genes : TreeFamFAM74A7
HOVERGENA6NL05
HOGENOMA6NL05
Homologs : HomoloGeneFAM74A7
Homology/Alignments : Family Browser (UCSC)FAM74A7
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerFAM74A7 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)FAM74A7
dbVarFAM74A7
ClinVarFAM74A7
1000_GenomesFAM74A7 
Exome Variant ServerFAM74A7
ExAC (Exome Aggregation Consortium)FAM74A7 (select the gene name)
Genetic variants : HAPMAP100996582
Genomic Variants (DGV)FAM74A7 [DGVbeta]
DECIPHERFAM74A7 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisFAM74A7 
Mutations
ICGC Data PortalFAM74A7 
TCGA Data PortalFAM74A7 
Broad Tumor PortalFAM74A7
OASIS PortalFAM74A7 [ Somatic mutations - Copy number]
Mutations and Diseases : HGMDFAM74A7
BioMutasearch FAM74A7
DgiDB (Drug Gene Interaction Database)FAM74A7
DoCM (Curated mutations)FAM74A7 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)FAM74A7 (select a term)
intoGenFAM74A7
Cancer3DFAM74A7(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenFAM74A7
Genetic Testing Registry FAM74A7
NextProtA6NL05 [Medical]
TSGene100996582
GENETestsFAM74A7
Target ValidationFAM74A7
Huge Navigator FAM74A7 [HugePedia]
snp3D : Map Gene to Disease100996582
BioCentury BCIQFAM74A7
ClinGenFAM74A7
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100996582
Clinical trialFAM74A7
Miscellaneous
canSAR (ICR)FAM74A7 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineFAM74A7
EVEXFAM74A7
GoPubMedFAM74A7
iHOPFAM74A7
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 : Mon Sep 18 13:08:11 CEST 2017

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