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TMEM191C (transmembrane protein 191C)

Identity

Alias (NCBI)-
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)
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)TMEM191C   33601
Cards
Entrez_Gene (NCBI)TMEM191C    transmembrane protein 191C
Aliases
GeneCards (Weizmann)TMEM191C
Ensembl hg19 (Hinxton)ENSG00000206140 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000206140 [Gene_View]  ENSG00000206140 [Sequence]  chr22:21467170-21469935 [Contig_View]  TMEM191C [Vega]
ICGC DataPortalENSG00000206140
TCGA cBioPortalTMEM191C
AceView (NCBI)TMEM191C
Genatlas (Paris)TMEM191C
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)
GoldenPathTMEM191C - 22q11.21 [CytoView hg19]  TMEM191C - 22q11.21 [CytoView hg38]
ImmunoBaseENSG00000206140
Genome Data Viewer NCBITMEM191C [Mapview hg19]  
Gene and transcription
Genbank (Entrez)AK094309 AK094490 AK308704 AL041322 BI827697
RefSeq transcript (Entrez)NM_001207052 NM_001388354
Consensus coding sequences : CCDS (NCBI)TMEM191C
Gene ExpressionTMEM191C [ NCBI-GEO ]   TMEM191C [ EBI - ARRAY_EXPRESS ]   TMEM191C [ SEEK ]   TMEM191C [ MEM ]
Gene Expression Viewer (FireBrowse)TMEM191C [ Firebrowse - Broad ]
GenevisibleExpression of TMEM191C in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)645426
GTEX Portal (Tissue expression)TMEM191C
Human Protein AtlasENSG00000206140-TMEM191C [pathology]   [cell]   [tissue]
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
PhosPhoSitePlusA6NGB0
Domains : Interpro (EBI)TMEM191B/C   
Domain families : Pfam (Sanger)TMEM191C (PF15194)   
Domain families : Pfam (NCBI)pfam15194   
Conserved Domain (NCBI)TMEM191C
SuperfamilyA6NGB0
AlphaFold pdb e-kbA6NGB0   
Human Protein Atlas [tissue]ENSG00000206140-TMEM191C [tissue]
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
GeneTree (enSembl)ENSG00000206140
Phylogenetic Trees/Animal Genes : TreeFamTMEM191C
Homologs : HomoloGeneTMEM191C
Homology/Alignments : Family Browser (UCSC)TMEM191C
Gene fusions - Rearrangements
Fusion : QuiverTMEM191C
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerTMEM191C [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)TMEM191C
dbVarTMEM191C
ClinVarTMEM191C
MonarchTMEM191C
1000_GenomesTMEM191C 
Exome Variant ServerTMEM191C
GNOMAD BrowserENSG00000206140
Varsome BrowserTMEM191C
ACMGTMEM191C variants
VarityA6NGB0
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]
Somatic Mutations in Cancer : COSMICTMEM191C  [overview]  [genome browser]  [tissue]  [distribution]  
Somatic Mutations in Cancer : COSMIC3DTMEM191C
Mutations and Diseases : HGMDTMEM191C
LOVD (Leiden Open Variation Database)[gene] [transcripts] [variants]
BioMutaTMEM191C
DgiDB (Drug Gene Interaction Database)TMEM191C
DoCM (Curated mutations)TMEM191C
CIViC (Clinical Interpretations of Variants in Cancer)TMEM191C
Cancer3DTMEM191C
Impact of mutations[PolyPhen2] [Provean] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
DisGeNETTMEM191C
MedgenTMEM191C
Genetic Testing Registry TMEM191C
NextProtA6NGB0 [Medical]
GENETestsTMEM191C
Target ValidationTMEM191C
Huge Navigator TMEM191C [HugePedia]
ClinGenTMEM191C
Clinical trials, drugs, therapy
MyCancerGenomeTMEM191C
Protein Interactions : CTDTMEM191C
Pharm GKB GenePA164726513
PharosA6NGB0
Clinical trialTMEM191C
Miscellaneous
canSAR (ICR)TMEM191C
HarmonizomeTMEM191C
DataMed IndexTMEM191C
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
EVEXTMEM191C
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

Search in all EBI   NCBI

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indexed on : Mon Oct 4 16:25:57 CEST 2021

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