Atlas of Genetics and Cytogenetics in Oncology and Haematology


Home   Genes   Leukemias   Solid Tumors   Cancer-Prone   Deep Insight   Case Reports   Journals  Portal   Teaching   

X Y 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 NA

TMEM191B (transmembrane protein 191B)

Identity

Alias (NCBI)-
HGNC (Hugo) TMEM191B
LocusID (NCBI) 728229
Atlas_Id 74858
Location 22q11.21  [Link to chromosome band 22q11]
Location_base_pair Starts at 18527802 and ends at 18530573 bp from pter ( according to hg38-Dec_2013)
Fusion genes
(updated 2017)
Data from Atlas, Mitelman, Cosmic Fusion, Fusion Cancer, TCGA fusion databases with official HUGO symbols (see references in chromosomal bands)

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    transmembrane protein 191B
Aliases
GeneCards (Weizmann)TMEM191B
Ensembl hg19 (Hinxton)ENSG00000278558 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000278558 [Gene_View]  ENSG00000278558 [Sequence]  chr22:18527802-18530573 [Contig_View]  TMEM191B [Vega]
ICGC DataPortalENSG00000278558
TCGA cBioPortalTMEM191B
AceView (NCBI)TMEM191B
Genatlas (Paris)TMEM191B
SOURCE (Princeton)TMEM191B
Genetics Home Reference (NIH)TMEM191B
Genomic and cartography
GoldenPath hg38 (UCSC)TMEM191B  -     chr22:18527802-18530573 +  22q11.21   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)TMEM191B  -     22q11.21   [Description]    (hg19-Feb_2009)
GoldenPathTMEM191B - 22q11.21 [CytoView hg19]  TMEM191B - 22q11.21 [CytoView hg38]
ImmunoBaseENSG00000278558
Genome Data Viewer NCBITMEM191B [Mapview hg19]  
Gene and transcription
Genbank (Entrez)AK093171
RefSeq transcript (Entrez)NM_001242313
Consensus coding sequences : CCDS (NCBI)TMEM191B
Gene ExpressionTMEM191B [ NCBI-GEO ]   TMEM191B [ EBI - ARRAY_EXPRESS ]   TMEM191B [ SEEK ]   TMEM191B [ MEM ]
Gene Expression Viewer (FireBrowse)TMEM191B [ Firebrowse - Broad ]
GenevisibleExpression of TMEM191B in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)728229
GTEX Portal (Tissue expression)TMEM191B
Human Protein AtlasENSG00000278558-TMEM191B [pathology]   [cell]   [tissue]
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
PhosPhoSitePlusP0C7N4
Domains : Interpro (EBI)TMEM191B/C   
Domain families : Pfam (Sanger)TMEM191C (PF15194)   
Domain families : Pfam (NCBI)pfam15194   
Conserved Domain (NCBI)TMEM191B
SuperfamilyP0C7N4
AlphaFold pdb e-kbP0C7N4   
Human Protein Atlas [tissue]ENSG00000278558-TMEM191B [tissue]
Protein Interaction databases
DIP (DOE-UCLA)P0C7N4
IntAct (EBI)P0C7N4
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
Homologs : HomoloGeneTMEM191B
Homology/Alignments : Family Browser (UCSC)TMEM191B
Gene fusions - Rearrangements
Fusion : QuiverTMEM191B
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerTMEM191B [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)TMEM191B
dbVarTMEM191B
ClinVarTMEM191B
MonarchTMEM191B
1000_GenomesTMEM191B 
Exome Variant ServerTMEM191B
GNOMAD BrowserENSG00000278558
Varsome BrowserTMEM191B
ACMGTMEM191B variants
VarityP0C7N4
Genomic Variants (DGV)TMEM191B [DGVbeta]
DECIPHERTMEM191B [patients]   [syndromes]   [variants]   [genes]  
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)[gene] [transcripts] [variants]
BioMutaTMEM191B
DgiDB (Drug Gene Interaction Database)TMEM191B
DoCM (Curated mutations)TMEM191B
CIViC (Clinical Interpretations of Variants in Cancer)TMEM191B
Cancer3DTMEM191B
Impact of mutations[PolyPhen2] [Provean] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
DisGeNETTMEM191B
MedgenTMEM191B
Genetic Testing Registry TMEM191B
NextProtP0C7N4 [Medical]
GENETestsTMEM191B
Target ValidationTMEM191B
Huge Navigator TMEM191B [HugePedia]
ClinGenTMEM191B
Clinical trials, drugs, therapy
MyCancerGenomeTMEM191B
Protein Interactions : CTDTMEM191B
Pharm GKB GenePA162406248
PharosP0C7N4
Clinical trialTMEM191B
Miscellaneous
canSAR (ICR)TMEM191B
HarmonizomeTMEM191B
DataMed IndexTMEM191B
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
EVEXTMEM191B
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

Search in all EBI   NCBI

© Atlas of Genetics and Cytogenetics in Oncology and Haematology
indexed on : Mon Oct 4 16:25:57 CEST 2021

Home   Genes   Leukemias   Solid Tumors   Cancer-Prone   Deep Insight   Case Reports   Journals  Portal   Teaching   

For comments and suggestions or contributions, please contact us

jlhuret@AtlasGeneticsOncology.org.