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TMEM191C (transmembrane protein 191C)

Identity

Other alias-
HGNC (Hugo) TMEM191C
LocusID (NCBI) 645426
Atlas_Id 74859
Location 22q11.21  [Link to chromosome band 22q11]
Location_base_pair Starts at 21467170 and ends at 21469935 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)TMEM191C   33601
Cards
Entrez_Gene (NCBI)TMEM191C  645426  transmembrane protein 191C
Aliases
GeneCards (Weizmann)TMEM191C
Ensembl hg19 (Hinxton) [Gene_View]
Ensembl hg38 (Hinxton) [Gene_View]  chr22:21467170-21469935 [Contig_View]  TMEM191C [Vega]
TCGA cBioPortalTMEM191C
AceView (NCBI)TMEM191C
Genatlas (Paris)TMEM191C
WikiGenes645426
SOURCE (Princeton)TMEM191C
Genetics Home Reference (NIH)TMEM191C
Genomic and cartography
GoldenPath hg38 (UCSC)TMEM191C  -     chr22:21467170-21469935 +  22q11.21   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)TMEM191C  -     22q11.21   [Description]    (hg19-Feb_2009)
EnsemblTMEM191C - 22q11.21 [CytoView hg19]  TMEM191C - 22q11.21 [CytoView hg38]
Mapping of homologs : NCBITMEM191C [Mapview hg19]  TMEM191C [Mapview hg38]
Gene and transcription
Genbank (Entrez)AK094309 AK094490 AK308704 AL041322 BI827697
RefSeq transcript (Entrez)NM_001207052
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)TMEM191C
Cluster EST : UnigeneHs.645547 [ NCBI ]
CGAP (NCI)Hs.645547
Gene ExpressionTMEM191C [ NCBI-GEO ]   TMEM191C [ EBI - ARRAY_EXPRESS ]   TMEM191C [ SEEK ]   TMEM191C [ MEM ]
Gene Expression Viewer (FireBrowse)TMEM191C [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)645426
GTEX Portal (Tissue expression)TMEM191C
Protein : pattern, domain, 3D structure
UniProt/SwissProtA6NGB0   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtA6NGB0  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProA6NGB0
Splice isoforms : SwissVarA6NGB0
PhosPhoSitePlusA6NGB0
Domains : Interpro (EBI)TMEM191B/C   
Domain families : Pfam (Sanger)TMEM191C (PF15194)   
Domain families : Pfam (NCBI)pfam15194   
Conserved Domain (NCBI)TMEM191C
DMDM Disease mutations645426
Blocks (Seattle)TMEM191C
SuperfamilyA6NGB0
Peptide AtlasA6NGB0
IPIIPI00935502   
Protein Interaction databases
DIP (DOE-UCLA)A6NGB0
IntAct (EBI)A6NGB0
BioGRIDTMEM191C
STRING (EMBL)TMEM191C
ZODIACTMEM191C
Ontologies - Pathways
QuickGOA6NGB0
Ontology : AmiGOintegral component of membrane  
Ontology : EGO-EBIintegral component of membrane  
NDEx NetworkTMEM191C
Atlas of Cancer Signalling NetworkTMEM191C
Wikipedia pathwaysTMEM191C
Orthology - Evolution
OrthoDB645426
Phylogenetic Trees/Animal Genes : TreeFamTMEM191C
HOVERGENA6NGB0
HOGENOMA6NGB0
Homologs : HomoloGeneTMEM191C
Homology/Alignments : Family Browser (UCSC)TMEM191C
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerTMEM191C [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)TMEM191C
dbVarTMEM191C
ClinVarTMEM191C
1000_GenomesTMEM191C 
Exome Variant ServerTMEM191C
ExAC (Exome Aggregation Consortium)TMEM191C (select the gene name)
Genetic variants : HAPMAP645426
Genomic Variants (DGV)TMEM191C [DGVbeta]
DECIPHERTMEM191C [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisTMEM191C 
Mutations
ICGC Data PortalTMEM191C 
TCGA Data PortalTMEM191C 
Broad Tumor PortalTMEM191C
OASIS PortalTMEM191C [ Somatic mutations - Copy number]
Mutations and Diseases : HGMDTMEM191C
BioMutasearch TMEM191C
DgiDB (Drug Gene Interaction Database)TMEM191C
DoCM (Curated mutations)TMEM191C (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)TMEM191C (select a term)
intoGenTMEM191C
Cancer3DTMEM191C(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenTMEM191C
Genetic Testing Registry TMEM191C
NextProtA6NGB0 [Medical]
TSGene645426
GENETestsTMEM191C
Target ValidationTMEM191C
Huge Navigator TMEM191C [HugePedia]
snp3D : Map Gene to Disease645426
BioCentury BCIQTMEM191C
ClinGenTMEM191C
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD645426
Chemical/Pharm GKB GenePA164726513
Clinical trialTMEM191C
Miscellaneous
canSAR (ICR)TMEM191C (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineTMEM191C
EVEXTMEM191C
GoPubMedTMEM191C
iHOPTMEM191C
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 15:46:04 CEST 2017

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