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TMEM191B (transmembrane protein 191B)

Identity

Other alias-
HGNC (Hugo) TMEM191B
LocusID (NCBI) 728229
Atlas_Id 74858
Location 22q11.21  [Link to chromosome band 22q11]
Location_base_pair Starts at 20377669 and ends at 20380440 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)TMEM191B   33600
Cards
Entrez_Gene (NCBI)TMEM191B  728229  transmembrane protein 191B
Aliases
GeneCards (Weizmann)TMEM191B
Ensembl hg19 (Hinxton)ENSG00000278558 [Gene_View]  chr22:20377669-20380440 [Contig_View]  TMEM191B [Vega]
Ensembl hg38 (Hinxton)ENSG00000278558 [Gene_View]  chr22:20377669-20380440 [Contig_View]  TMEM191B [Vega]
ICGC DataPortalENSG00000278558
TCGA cBioPortalTMEM191B
AceView (NCBI)TMEM191B
Genatlas (Paris)TMEM191B
WikiGenes728229
SOURCE (Princeton)TMEM191B
Genetics Home Reference (NIH)TMEM191B
Genomic and cartography
GoldenPath hg19 (UCSC)TMEM191B  -     chr22:20377669-20380440 +  22q11.21   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)TMEM191B  -     22q11.21   [Description]    (hg38-Dec_2013)
EnsemblTMEM191B - 22q11.21 [CytoView hg19]  TMEM191B - 22q11.21 [CytoView hg38]
Mapping of homologs : NCBITMEM191B [Mapview hg19]  TMEM191B [Mapview hg38]
Gene and transcription
Genbank (Entrez)AK093171
RefSeq transcript (Entrez)NM_001242313
RefSeq genomic (Entrez)NC_000022 NC_018933 NT_187357 NW_004929429
Consensus coding sequences : CCDS (NCBI)TMEM191B
Cluster EST : UnigeneHs.376511 [ NCBI ]
CGAP (NCI)Hs.376511
Alternative Splicing GalleryENSG00000278558
Gene ExpressionTMEM191B [ NCBI-GEO ]   TMEM191B [ EBI - ARRAY_EXPRESS ]   TMEM191B [ SEEK ]   TMEM191B [ MEM ]
Gene Expression Viewer (FireBrowse)TMEM191B [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)728229
GTEX Portal (Tissue expression)TMEM191B
Protein : pattern, domain, 3D structure
UniProt/SwissProtP0C7N4   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtP0C7N4  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProP0C7N4
Splice isoforms : SwissVarP0C7N4
PhosPhoSitePlusP0C7N4
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)TMEM191B
DMDM Disease mutations728229
Blocks (Seattle)TMEM191B
SuperfamilyP0C7N4
Human Protein AtlasENSG00000278558
Peptide AtlasP0C7N4
IPIIPI00895867   IPI00645781   
Protein Interaction databases
DIP (DOE-UCLA)P0C7N4
IntAct (EBI)P0C7N4
FunCoupENSG00000278558
BioGRIDTMEM191B
STRING (EMBL)TMEM191B
ZODIACTMEM191B
Ontologies - Pathways
QuickGOP0C7N4
Ontology : AmiGOintegral component of membrane  
Ontology : EGO-EBIintegral component of membrane  
NDEx NetworkTMEM191B
Atlas of Cancer Signalling NetworkTMEM191B
Wikipedia pathwaysTMEM191B
Orthology - Evolution
OrthoDB728229
GeneTree (enSembl)ENSG00000278558
Phylogenetic Trees/Animal Genes : TreeFamTMEM191B
HOVERGENP0C7N4
HOGENOMP0C7N4
Homologs : HomoloGeneTMEM191B
Homology/Alignments : Family Browser (UCSC)TMEM191B
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerTMEM191B [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)TMEM191B
dbVarTMEM191B
ClinVarTMEM191B
1000_GenomesTMEM191B 
Exome Variant ServerTMEM191B
ExAC (Exome Aggregation Consortium)TMEM191B (select the gene name)
Genetic variants : HAPMAP728229
Genomic Variants (DGV)TMEM191B [DGVbeta]
DECIPHER (Syndromes)22:20377669-20380440  ENSG00000278558
CONAN: Copy Number AnalysisTMEM191B 
Mutations
ICGC Data PortalTMEM191B 
TCGA Data PortalTMEM191B 
Broad Tumor PortalTMEM191B
OASIS PortalTMEM191B [ Somatic mutations - Copy number]
Mutations and Diseases : HGMDTMEM191B
LOVD (Leiden Open Variation Database)Whole genome datasets
LOVD (Leiden Open Variation Database)LOVD 3.0 shared installation
BioMutasearch TMEM191B
DgiDB (Drug Gene Interaction Database)TMEM191B
DoCM (Curated mutations)TMEM191B (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)TMEM191B (select a term)
intoGenTMEM191B
Cancer3DTMEM191B(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenTMEM191B
Genetic Testing Registry TMEM191B
NextProtP0C7N4 [Medical]
TSGene728229
GENETestsTMEM191B
Huge Navigator TMEM191B [HugePedia]
snp3D : Map Gene to Disease728229
BioCentury BCIQTMEM191B
ClinGenTMEM191B
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD728229
Chemical/Pharm GKB GenePA162406248
Clinical trialTMEM191B
Miscellaneous
canSAR (ICR)TMEM191B (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineTMEM191B
EVEXTMEM191B
GoPubMedTMEM191B
iHOPTMEM191B
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 : Tue Mar 14 12:48:39 CET 2017

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