Atlas of Genetics and Cytogenetics in Oncology and Haematology


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TMEM68 (transmembrane protein 68)

Identity

Alias (NCBI)-
HGNC (Hugo) TMEM68
HGNC Alias symbFLJ32370
LocusID (NCBI) 137695
Atlas_Id 74970
Location 8q12.1  [Link to chromosome band 8q12]
Location_base_pair Starts at 55738759 and ends at 55773378 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)
ERLIN2 (8p11.23) / TMEM68 (8q12.1)TMEM68 (8q12.1) / ERCC3 (2q14.3)TMEM68 (8q12.1) / PEX5L (3q26.33)
TMEM68 (8q12.1) / TMEM68 (8q12.1)TMEM68 (8q12.1) / ZNF821 (16q22.2)

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)TMEM68   26510
Cards
Entrez_Gene (NCBI)TMEM68    transmembrane protein 68
Aliases
GeneCards (Weizmann)TMEM68
Ensembl hg19 (Hinxton)ENSG00000167904 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000167904 [Gene_View]  ENSG00000167904 [Sequence]  chr8:55738759-55773378 [Contig_View]  TMEM68 [Vega]
ICGC DataPortalENSG00000167904
TCGA cBioPortalTMEM68
AceView (NCBI)TMEM68
Genatlas (Paris)TMEM68
SOURCE (Princeton)TMEM68
Genetics Home Reference (NIH)TMEM68
Genomic and cartography
GoldenPath hg38 (UCSC)TMEM68  -     chr8:55738759-55773378 -  8q12.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)TMEM68  -     8q12.1   [Description]    (hg19-Feb_2009)
GoldenPathTMEM68 - 8q12.1 [CytoView hg19]  TMEM68 - 8q12.1 [CytoView hg38]
ImmunoBaseENSG00000167904
Genome Data Viewer NCBITMEM68 [Mapview hg19]  
Gene and transcription
Genbank (Entrez)AF147306 AK056932 AK308247 AL832935 BC020835
RefSeq transcript (Entrez)NM_001286657 NM_001286660 NM_001286661 NM_001363176 NM_001363177 NM_152417
Consensus coding sequences : CCDS (NCBI)TMEM68
Gene ExpressionTMEM68 [ NCBI-GEO ]   TMEM68 [ EBI - ARRAY_EXPRESS ]   TMEM68 [ SEEK ]   TMEM68 [ MEM ]
Gene Expression Viewer (FireBrowse)TMEM68 [ Firebrowse - Broad ]
GenevisibleExpression of TMEM68 in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)137695
GTEX Portal (Tissue expression)TMEM68
Human Protein AtlasENSG00000167904-TMEM68 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ96MH6   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ96MH6  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ96MH6
PhosPhoSitePlusQ96MH6
Domains : Interpro (EBI)Plipid/glycerol_acylTrfase   
Domain families : Pfam (Sanger)Acyltransferase (PF01553)   
Domain families : Pfam (NCBI)pfam01553   
Conserved Domain (NCBI)TMEM68
SuperfamilyQ96MH6
AlphaFold pdb e-kbQ96MH6   
Human Protein Atlas [tissue]ENSG00000167904-TMEM68 [tissue]
HPRD08128
Protein Interaction databases
DIP (DOE-UCLA)Q96MH6
IntAct (EBI)Q96MH6
BioGRIDTMEM68
STRING (EMBL)TMEM68
ZODIACTMEM68
Ontologies - Pathways
QuickGOQ96MH6
Ontology : AmiGOintegral component of membrane  acyltransferase activity  
Ontology : EGO-EBIintegral component of membrane  acyltransferase activity  
NDEx NetworkTMEM68
Atlas of Cancer Signalling NetworkTMEM68
Wikipedia pathwaysTMEM68
Orthology - Evolution
OrthoDB137695
GeneTree (enSembl)ENSG00000167904
Phylogenetic Trees/Animal Genes : TreeFamTMEM68
Homologs : HomoloGeneTMEM68
Homology/Alignments : Family Browser (UCSC)TMEM68
Gene fusions - Rearrangements
Fusion : QuiverTMEM68
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerTMEM68 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)TMEM68
dbVarTMEM68
ClinVarTMEM68
MonarchTMEM68
1000_GenomesTMEM68 
Exome Variant ServerTMEM68
GNOMAD BrowserENSG00000167904
Varsome BrowserTMEM68
ACMGTMEM68 variants
VarityQ96MH6
Genomic Variants (DGV)TMEM68 [DGVbeta]
DECIPHERTMEM68 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisTMEM68 
Mutations
ICGC Data PortalTMEM68 
TCGA Data PortalTMEM68 
Broad Tumor PortalTMEM68
OASIS PortalTMEM68 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICTMEM68  [overview]  [genome browser]  [tissue]  [distribution]  
Somatic Mutations in Cancer : COSMIC3DTMEM68
Mutations and Diseases : HGMDTMEM68
LOVD (Leiden Open Variation Database)[gene] [transcripts] [variants]
BioMutaTMEM68
DgiDB (Drug Gene Interaction Database)TMEM68
DoCM (Curated mutations)TMEM68
CIViC (Clinical Interpretations of Variants in Cancer)TMEM68
Cancer3DTMEM68
Impact of mutations[PolyPhen2] [Provean] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
DisGeNETTMEM68
MedgenTMEM68
Genetic Testing Registry TMEM68
NextProtQ96MH6 [Medical]
GENETestsTMEM68
Target ValidationTMEM68
Huge Navigator TMEM68 [HugePedia]
ClinGenTMEM68
Clinical trials, drugs, therapy
MyCancerGenomeTMEM68
Protein Interactions : CTDTMEM68
Pharm GKB GenePA142670781
PharosQ96MH6
Clinical trialTMEM68
Miscellaneous
canSAR (ICR)TMEM68
HarmonizomeTMEM68
DataMed IndexTMEM68
Probes
Litterature
PubMed14 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
EVEXTMEM68
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 16:26:19 CEST 2021

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