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FAM156A (family with sequence similarity 156 member A)

Identity

Alias_namesTMEM29
transmembrane protein 29
family with sequence similarity 156, member A
Alias_symbol (synonym)PRO0659
Other alias
HGNC (Hugo) FAM156A
LocusID (NCBI) 29057
Atlas_Id 63046
Location Xp11.22  [Link to chromosome band Xp11]
Location_base_pair Starts at 52947256 and ends at 52995472 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)FAM156A   30114
Cards
Entrez_Gene (NCBI)FAM156A  29057  family with sequence similarity 156 member A
AliasesPRO0659; TMEM29
GeneCards (Weizmann)FAM156A
Ensembl hg19 (Hinxton)ENSG00000268350 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000268350 [Gene_View]  chrX:52947256-52995472 [Contig_View]  FAM156A [Vega]
ICGC DataPortalENSG00000268350
TCGA cBioPortalFAM156A
AceView (NCBI)FAM156A
Genatlas (Paris)FAM156A
WikiGenes29057
SOURCE (Princeton)FAM156A
Genetics Home Reference (NIH)FAM156A
Genomic and cartography
GoldenPath hg38 (UCSC)FAM156A  -     chrX:52947256-52995472 -  Xp11.22   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)FAM156A  -     Xp11.22   [Description]    (hg19-Feb_2009)
EnsemblFAM156A - Xp11.22 [CytoView hg19]  FAM156A - Xp11.22 [CytoView hg38]
Mapping of homologs : NCBIFAM156A [Mapview hg19]  FAM156A [Mapview hg38]
Gene and transcription
Genbank (Entrez)AF090943 AF370413 AK054721 AK057692 AK092365
RefSeq transcript (Entrez)NM_001242489 NM_001242490 NM_001242491 NM_001242492 NM_001242493 NM_001242494 NM_001242495 NM_001242496 NM_001242497 NM_014138
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)FAM156A
Cluster EST : UnigeneHs.653131 [ NCBI ]
CGAP (NCI)Hs.653131
Alternative Splicing GalleryENSG00000268350
Gene ExpressionFAM156A [ NCBI-GEO ]   FAM156A [ EBI - ARRAY_EXPRESS ]   FAM156A [ SEEK ]   FAM156A [ MEM ]
Gene Expression Viewer (FireBrowse)FAM156A [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)29057
GTEX Portal (Tissue expression)FAM156A
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ8NDB6   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ8NDB6  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ8NDB6
Splice isoforms : SwissVarQ8NDB6
PhosPhoSitePlusQ8NDB6
Domains : Interpro (EBI)Dppa3   
Domain families : Pfam (Sanger)PGC7_Stella (PF15549)   
Domain families : Pfam (NCBI)pfam15549   
Conserved Domain (NCBI)FAM156A
DMDM Disease mutations29057
Blocks (Seattle)FAM156A
SuperfamilyQ8NDB6
Human Protein AtlasENSG00000268350
Peptide AtlasQ8NDB6
HPRD06683
IPIIPI00177432   IPI00645735   IPI00644137   IPI00644273   IPI00645259   IPI00647444   IPI01013909   IPI00965348   IPI01015158   IPI01009772   
Protein Interaction databases
DIP (DOE-UCLA)Q8NDB6
IntAct (EBI)Q8NDB6
FunCoupENSG00000268350
BioGRIDFAM156A
STRING (EMBL)FAM156A
ZODIACFAM156A
Ontologies - Pathways
QuickGOQ8NDB6
Ontology : AmiGOprotein binding  nuclear envelope  integral component of membrane  methylated histone binding  
Ontology : EGO-EBIprotein binding  nuclear envelope  integral component of membrane  methylated histone binding  
NDEx NetworkFAM156A
Atlas of Cancer Signalling NetworkFAM156A
Wikipedia pathwaysFAM156A
Orthology - Evolution
OrthoDB29057
GeneTree (enSembl)ENSG00000268350
Phylogenetic Trees/Animal Genes : TreeFamFAM156A
HOVERGENQ8NDB6
HOGENOMQ8NDB6
Homologs : HomoloGeneFAM156A
Homology/Alignments : Family Browser (UCSC)FAM156A
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerFAM156A [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)FAM156A
dbVarFAM156A
ClinVarFAM156A
1000_GenomesFAM156A 
Exome Variant ServerFAM156A
ExAC (Exome Aggregation Consortium)FAM156A (select the gene name)
Genetic variants : HAPMAP29057
Genomic Variants (DGV)FAM156A [DGVbeta]
DECIPHERFAM156A [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisFAM156A 
Mutations
ICGC Data PortalFAM156A 
TCGA Data PortalFAM156A 
Broad Tumor PortalFAM156A
OASIS PortalFAM156A [ Somatic mutations - Copy number]
Mutations and Diseases : HGMDFAM156A
LOVD (Leiden Open Variation Database)Whole genome datasets
LOVD (Leiden Open Variation Database)LOVD 3.0 shared installation
BioMutasearch FAM156A
DgiDB (Drug Gene Interaction Database)FAM156A
DoCM (Curated mutations)FAM156A (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)FAM156A (select a term)
intoGenFAM156A
Cancer3DFAM156A(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenFAM156A
Genetic Testing Registry FAM156A
NextProtQ8NDB6 [Medical]
TSGene29057
GENETestsFAM156A
Target ValidationFAM156A
Huge Navigator FAM156A [HugePedia]
snp3D : Map Gene to Disease29057
BioCentury BCIQFAM156A
ClinGenFAM156A
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD29057
Chemical/Pharm GKB GenePA162386698
Clinical trialFAM156A
Miscellaneous
canSAR (ICR)FAM156A (select the gene name)
Probes
Litterature
PubMed13 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineFAM156A
EVEXFAM156A
GoPubMedFAM156A
iHOPFAM156A
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 13:07:38 CEST 2017

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