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TMEM234 (transmembrane protein 234)

Identity

Alias (NCBI)AASL548
C1orf91
PRO1105
RP4-622L5
dJ622L5.7
HGNC (Hugo) TMEM234
HGNC Alias symbRP4-622L5
dJ622L5.7
FLJ90779
HGNC Previous nameC1orf91
HGNC Previous namechromosome 1 open reading frame 91
LocusID (NCBI) 56063
Atlas_Id 74898
Location 1p35.2  [Link to chromosome band 1p35]
Location_base_pair Starts at 32216200 and ends at 32222353 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)TMEM234   28837
Cards
Entrez_Gene (NCBI)TMEM234    transmembrane protein 234
AliasesAASL548; C1orf91; PRO1105; RP4-622L5; 
dJ622L5.7
GeneCards (Weizmann)TMEM234
Ensembl hg19 (Hinxton)ENSG00000160055 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000160055 [Gene_View]  ENSG00000160055 [Sequence]  chr1:32216200-32222353 [Contig_View]  TMEM234 [Vega]
ICGC DataPortalENSG00000160055
TCGA cBioPortalTMEM234
AceView (NCBI)TMEM234
Genatlas (Paris)TMEM234
SOURCE (Princeton)TMEM234
Genetics Home Reference (NIH)TMEM234
Genomic and cartography
GoldenPath hg38 (UCSC)TMEM234  -     chr1:32216200-32222353 -  1p35.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)TMEM234  -     1p35.2   [Description]    (hg19-Feb_2009)
GoldenPathTMEM234 - 1p35.2 [CytoView hg19]  TMEM234 - 1p35.2 [CytoView hg38]
ImmunoBaseENSG00000160055
Genome Data Viewer NCBITMEM234 [Mapview hg19]  
Gene and transcription
Genbank (Entrez)AF258548 AK075260 AK295232 AK312046 AL512700
RefSeq transcript (Entrez)NM_001366191 NM_019118
Consensus coding sequences : CCDS (NCBI)TMEM234
Gene ExpressionTMEM234 [ NCBI-GEO ]   TMEM234 [ EBI - ARRAY_EXPRESS ]   TMEM234 [ SEEK ]   TMEM234 [ MEM ]
Gene Expression Viewer (FireBrowse)TMEM234 [ Firebrowse - Broad ]
GenevisibleExpression of TMEM234 in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)56063
GTEX Portal (Tissue expression)TMEM234
Human Protein AtlasENSG00000160055-TMEM234 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ8WY98   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ8WY98  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ8WY98
PhosPhoSitePlusQ8WY98
Domains : Interpro (EBI)TMEM234   
Domain families : Pfam (Sanger)TMEM234 (PF10639)   
Domain families : Pfam (NCBI)pfam10639   
Conserved Domain (NCBI)TMEM234
SuperfamilyQ8WY98
AlphaFold pdb e-kbQ8WY98   
Human Protein Atlas [tissue]ENSG00000160055-TMEM234 [tissue]
HPRD15270
Protein Interaction databases
DIP (DOE-UCLA)Q8WY98
IntAct (EBI)Q8WY98
BioGRIDTMEM234
STRING (EMBL)TMEM234
ZODIACTMEM234
Ontologies - Pathways
QuickGOQ8WY98
Ontology : AmiGOprotein binding  integral component of membrane  
Ontology : EGO-EBIprotein binding  integral component of membrane  
NDEx NetworkTMEM234
Atlas of Cancer Signalling NetworkTMEM234
Wikipedia pathwaysTMEM234
Orthology - Evolution
OrthoDB56063
GeneTree (enSembl)ENSG00000160055
Phylogenetic Trees/Animal Genes : TreeFamTMEM234
Homologs : HomoloGeneTMEM234
Homology/Alignments : Family Browser (UCSC)TMEM234
Gene fusions - Rearrangements
Fusion : QuiverTMEM234
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerTMEM234 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)TMEM234
dbVarTMEM234
ClinVarTMEM234
MonarchTMEM234
1000_GenomesTMEM234 
Exome Variant ServerTMEM234
GNOMAD BrowserENSG00000160055
Varsome BrowserTMEM234
ACMGTMEM234 variants
VarityQ8WY98
Genomic Variants (DGV)TMEM234 [DGVbeta]
DECIPHERTMEM234 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisTMEM234 
Mutations
ICGC Data PortalTMEM234 
TCGA Data PortalTMEM234 
Broad Tumor PortalTMEM234
OASIS PortalTMEM234 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICTMEM234  [overview]  [genome browser]  [tissue]  [distribution]  
Somatic Mutations in Cancer : COSMIC3DTMEM234
Mutations and Diseases : HGMDTMEM234
LOVD (Leiden Open Variation Database)[gene] [transcripts] [variants]
BioMutaTMEM234
DgiDB (Drug Gene Interaction Database)TMEM234
DoCM (Curated mutations)TMEM234
CIViC (Clinical Interpretations of Variants in Cancer)TMEM234
Cancer3DTMEM234
Impact of mutations[PolyPhen2] [Provean] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
DisGeNETTMEM234
MedgenTMEM234
Genetic Testing Registry TMEM234
NextProtQ8WY98 [Medical]
GENETestsTMEM234
Target ValidationTMEM234
Huge Navigator TMEM234 [HugePedia]
ClinGenTMEM234
Clinical trials, drugs, therapy
MyCancerGenomeTMEM234
Protein Interactions : CTDTMEM234
Pharm GKB GenePA142672475
PharosQ8WY98
Clinical trialTMEM234
Miscellaneous
canSAR (ICR)TMEM234
HarmonizomeTMEM234
DataMed IndexTMEM234
Probes
Litterature
PubMed10 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
EVEXTMEM234
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 16:26:04 CEST 2021

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