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TMEM191A (transmembrane protein 191A (pseudogene))

Identity

Alias_namestransmembrane protein 191A
Alias_symbol (synonym)DKFZp434N035
TMEM191AP
Other alias
HGNC (Hugo) TMEM191A
LocusID (NCBI) 84222
Atlas_Id 74857
Location 22q11.21  [Link to chromosome band 22q11]
Location_base_pair Starts at 20700932 and ends at 20701667 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)TMEM191A   25317
Cards
Entrez_Gene (NCBI)TMEM191A  84222  transmembrane protein 191A (pseudogene)
AliasesTMEM191AP
GeneCards (Weizmann)TMEM191A
Ensembl hg19 (Hinxton)ENSG00000226287 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000226287 [Gene_View]  chr22:20700932-20701667 [Contig_View]  TMEM191A [Vega]
ICGC DataPortalENSG00000226287
TCGA cBioPortalTMEM191A
AceView (NCBI)TMEM191A
Genatlas (Paris)TMEM191A
WikiGenes84222
SOURCE (Princeton)TMEM191A
Genetics Home Reference (NIH)TMEM191A
Genomic and cartography
GoldenPath hg38 (UCSC)TMEM191A  -     chr22:20700932-20701667 +  22q11.21   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)TMEM191A  -     22q11.21   [Description]    (hg19-Feb_2009)
EnsemblTMEM191A - 22q11.21 [CytoView hg19]  TMEM191A - 22q11.21 [CytoView hg38]
Mapping of homologs : NCBITMEM191A [Mapview hg19]  TMEM191A [Mapview hg38]
Gene and transcription
Genbank (Entrez)AK313335 AL136879 BC126323 BC126325 CR456359
RefSeq transcript (Entrez)NM_032262
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)TMEM191A
Cluster EST : UnigeneHs.546454 [ NCBI ]
CGAP (NCI)Hs.546454
Alternative Splicing GalleryENSG00000226287
Gene ExpressionTMEM191A [ NCBI-GEO ]   TMEM191A [ EBI - ARRAY_EXPRESS ]   TMEM191A [ SEEK ]   TMEM191A [ MEM ]
Gene Expression Viewer (FireBrowse)TMEM191A [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)84222
GTEX Portal (Tissue expression)TMEM191A
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ9H0A3   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ9H0A3  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ9H0A3
Splice isoforms : SwissVarQ9H0A3
PhosPhoSitePlusQ9H0A3
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)TMEM191A
DMDM Disease mutations84222
Blocks (Seattle)TMEM191A
SuperfamilyQ9H0A3
Human Protein AtlasENSG00000226287
Peptide AtlasQ9H0A3
HPRD13197
IPIIPI00031046   
Protein Interaction databases
DIP (DOE-UCLA)Q9H0A3
IntAct (EBI)Q9H0A3
FunCoupENSG00000226287
BioGRIDTMEM191A
STRING (EMBL)TMEM191A
ZODIACTMEM191A
Ontologies - Pathways
QuickGOQ9H0A3
Ontology : AmiGOintegral component of membrane  
Ontology : EGO-EBIintegral component of membrane  
NDEx NetworkTMEM191A
Atlas of Cancer Signalling NetworkTMEM191A
Wikipedia pathwaysTMEM191A
Orthology - Evolution
OrthoDB84222
GeneTree (enSembl)ENSG00000226287
Phylogenetic Trees/Animal Genes : TreeFamTMEM191A
HOVERGENQ9H0A3
HOGENOMQ9H0A3
Homologs : HomoloGeneTMEM191A
Homology/Alignments : Family Browser (UCSC)TMEM191A
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerTMEM191A [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)TMEM191A
dbVarTMEM191A
ClinVarTMEM191A
1000_GenomesTMEM191A 
Exome Variant ServerTMEM191A
ExAC (Exome Aggregation Consortium)TMEM191A (select the gene name)
Genetic variants : HAPMAP84222
Genomic Variants (DGV)TMEM191A [DGVbeta]
DECIPHERTMEM191A [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisTMEM191A 
Mutations
ICGC Data PortalTMEM191A 
TCGA Data PortalTMEM191A 
Broad Tumor PortalTMEM191A
OASIS PortalTMEM191A [ Somatic mutations - Copy number]
Mutations and Diseases : HGMDTMEM191A
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 TMEM191A
DgiDB (Drug Gene Interaction Database)TMEM191A
DoCM (Curated mutations)TMEM191A (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)TMEM191A (select a term)
intoGenTMEM191A
Cancer3DTMEM191A(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenTMEM191A
Genetic Testing Registry TMEM191A
NextProtQ9H0A3 [Medical]
TSGene84222
GENETestsTMEM191A
Target ValidationTMEM191A
Huge Navigator TMEM191A [HugePedia]
snp3D : Map Gene to Disease84222
BioCentury BCIQTMEM191A
ClinGenTMEM191A
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD84222
Chemical/Pharm GKB GenePA164726509
Clinical trialTMEM191A
Miscellaneous
canSAR (ICR)TMEM191A (select the gene name)
Probes
Litterature
PubMed4 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineTMEM191A
EVEXTMEM191A
GoPubMedTMEM191A
iHOPTMEM191A
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 : Wed May 31 15:46:03 CEST 2017

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