Atlas of Genetics and Cytogenetics in Oncology and Haematology


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TMEM251 (transmembrane protein 251)

Identity

Alias (NCBI)C14orf109
DMAN
HGNC (Hugo) TMEM251
HGNC Alias symbDKFZP564F1123
HGNC Previous nameC14orf109
HGNC Previous namechromosome 14 open reading frame 109
LocusID (NCBI) 26175
Atlas_Id 74914
Location 14q32.12  [Link to chromosome band 14q32]
Location_base_pair Starts at 93184974 and ends at 93188463 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)
TMEM251 (14q32.12) / UBR7 (14q32.12)

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)TMEM251   20218
Cards
Entrez_Gene (NCBI)TMEM251    transmembrane protein 251
AliasesC14orf109; DMAN
GeneCards (Weizmann)TMEM251
Ensembl hg19 (Hinxton)ENSG00000153485 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000153485 [Gene_View]  ENSG00000153485 [Sequence]  chr14:93184974-93188463 [Contig_View]  TMEM251 [Vega]
ICGC DataPortalENSG00000153485
TCGA cBioPortalTMEM251
AceView (NCBI)TMEM251
Genatlas (Paris)TMEM251
SOURCE (Princeton)TMEM251
Genetics Home Reference (NIH)TMEM251
Genomic and cartography
GoldenPath hg38 (UCSC)TMEM251  -     chr14:93184974-93188463 +  14q32.12   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)TMEM251  -     14q32.12   [Description]    (hg19-Feb_2009)
GoldenPathTMEM251 - 14q32.12 [CytoView hg19]  TMEM251 - 14q32.12 [CytoView hg38]
ImmunoBaseENSG00000153485
Genome Data Viewer NCBITMEM251 [Mapview hg19]  
OMIM619332   619345   
Gene and transcription
Genbank (Entrez)AI056285 AL080118 AW404266 BC030119 BP398505
RefSeq transcript (Entrez)NM_001098621 NM_015676
Consensus coding sequences : CCDS (NCBI)TMEM251
Gene ExpressionTMEM251 [ NCBI-GEO ]   TMEM251 [ EBI - ARRAY_EXPRESS ]   TMEM251 [ SEEK ]   TMEM251 [ MEM ]
Gene Expression Viewer (FireBrowse)TMEM251 [ Firebrowse - Broad ]
GenevisibleExpression of TMEM251 in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)26175
GTEX Portal (Tissue expression)TMEM251
Human Protein AtlasENSG00000153485-TMEM251 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ8N6I4   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ8N6I4  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ8N6I4
PhosPhoSitePlusQ8N6I4
Domains : Interpro (EBI)TMEM251   
Domain families : Pfam (Sanger)TMEM251 (PF15190)   
Domain families : Pfam (NCBI)pfam15190   
Conserved Domain (NCBI)TMEM251
SuperfamilyQ8N6I4
AlphaFold pdb e-kbQ8N6I4   
Human Protein Atlas [tissue]ENSG00000153485-TMEM251 [tissue]
Protein Interaction databases
DIP (DOE-UCLA)Q8N6I4
IntAct (EBI)Q8N6I4
BioGRIDTMEM251
STRING (EMBL)TMEM251
ZODIACTMEM251
Ontologies - Pathways
QuickGOQ8N6I4
Ontology : AmiGOintegral component of membrane  
Ontology : EGO-EBIintegral component of membrane  
NDEx NetworkTMEM251
Atlas of Cancer Signalling NetworkTMEM251
Wikipedia pathwaysTMEM251
Orthology - Evolution
OrthoDB26175
GeneTree (enSembl)ENSG00000153485
Phylogenetic Trees/Animal Genes : TreeFamTMEM251
Homologs : HomoloGeneTMEM251
Homology/Alignments : Family Browser (UCSC)TMEM251
Gene fusions - Rearrangements
Fusion : QuiverTMEM251
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerTMEM251 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)TMEM251
dbVarTMEM251
ClinVarTMEM251
MonarchTMEM251
1000_GenomesTMEM251 
Exome Variant ServerTMEM251
GNOMAD BrowserENSG00000153485
Varsome BrowserTMEM251
ACMGTMEM251 variants
VarityQ8N6I4
Genomic Variants (DGV)TMEM251 [DGVbeta]
DECIPHERTMEM251 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisTMEM251 
Mutations
ICGC Data PortalTMEM251 
TCGA Data PortalTMEM251 
Broad Tumor PortalTMEM251
OASIS PortalTMEM251 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICTMEM251  [overview]  [genome browser]  [tissue]  [distribution]  
Somatic Mutations in Cancer : COSMIC3DTMEM251
Mutations and Diseases : HGMDTMEM251
LOVD (Leiden Open Variation Database)[gene] [transcripts] [variants]
BioMutaTMEM251
DgiDB (Drug Gene Interaction Database)TMEM251
DoCM (Curated mutations)TMEM251
CIViC (Clinical Interpretations of Variants in Cancer)TMEM251
Cancer3DTMEM251
Impact of mutations[PolyPhen2] [Provean] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM619332    619345   
Orphanet
DisGeNETTMEM251
MedgenTMEM251
Genetic Testing Registry TMEM251
NextProtQ8N6I4 [Medical]
GENETestsTMEM251
Target ValidationTMEM251
Huge Navigator TMEM251 [HugePedia]
ClinGenTMEM251
Clinical trials, drugs, therapy
MyCancerGenomeTMEM251
Protein Interactions : CTDTMEM251
Pharm GKB GenePA134977710
PharosQ8N6I4
Clinical trialTMEM251
Miscellaneous
canSAR (ICR)TMEM251
HarmonizomeTMEM251
DataMed IndexTMEM251
Probes
Litterature
PubMed3 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
EVEXTMEM251
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Mon Oct 4 16:26:07 CEST 2021

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