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NUTM2G (NUT family member 2G)

Identity

Alias_namesFAM22G
family with sequence similarity 22, member G
Other aliasNUTMG
HGNC (Hugo) NUTM2G
LocusID (NCBI) 441457
Atlas_Id 71057
Location 9q22.33  [Link to chromosome band 9q22]
Location_base_pair Starts at 99691286 and ends at 99704572 bp from pter ( according to hg19-Feb_2009)

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)NUTM2G   23449
Cards
Entrez_Gene (NCBI)NUTM2G  441457  NUT family member 2G
AliasesFAM22G; NUTMG
GeneCards (Weizmann)NUTM2G
Ensembl hg19 (Hinxton)ENSG00000188152 [Gene_View]  chr9:99691286-99704572 [Contig_View]  NUTM2G [Vega]
Ensembl hg38 (Hinxton)ENSG00000188152 [Gene_View]  chr9:99691286-99704572 [Contig_View]  NUTM2G [Vega]
ICGC DataPortalENSG00000188152
TCGA cBioPortalNUTM2G
AceView (NCBI)NUTM2G
Genatlas (Paris)NUTM2G
WikiGenes441457
SOURCE (Princeton)NUTM2G
Genetics Home Reference (NIH)NUTM2G
Genomic and cartography
GoldenPath hg19 (UCSC)NUTM2G  -     chr9:99691286-99704572 +  9q22.33   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)NUTM2G  -     9q22.33   [Description]    (hg38-Dec_2013)
EnsemblNUTM2G - 9q22.33 [CytoView hg19]  NUTM2G - 9q22.33 [CytoView hg38]
Mapping of homologs : NCBINUTM2G [Mapview hg19]  NUTM2G [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)NM_001045477 NM_001170741
RefSeq genomic (Entrez)NC_000009 NC_018920 NT_008470 NW_004929366
Consensus coding sequences : CCDS (NCBI)NUTM2G
Cluster EST : UnigeneHs.652383 [ NCBI ]
CGAP (NCI)Hs.652383
Alternative Splicing GalleryENSG00000188152
Gene ExpressionNUTM2G [ NCBI-GEO ]   NUTM2G [ EBI - ARRAY_EXPRESS ]   NUTM2G [ SEEK ]   NUTM2G [ MEM ]
Gene Expression Viewer (FireBrowse)NUTM2G [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)441457
GTEX Portal (Tissue expression)NUTM2G
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ5VZR2   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ5VZR2  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ5VZR2
Splice isoforms : SwissVarQ5VZR2
PhosPhoSitePlusQ5VZR2
Domains : Interpro (EBI)NUT/FAM22    NUT_C    NUT_N   
Domain families : Pfam (Sanger)NUT_C (PF12882)    NUT_N (PF12881)   
Domain families : Pfam (NCBI)pfam12882    pfam12881   
Conserved Domain (NCBI)NUTM2G
DMDM Disease mutations441457
Blocks (Seattle)NUTM2G
SuperfamilyQ5VZR2
Human Protein AtlasENSG00000188152
Peptide AtlasQ5VZR2
IPIIPI00456827   IPI00472489   IPI00253046   
Protein Interaction databases
DIP (DOE-UCLA)Q5VZR2
IntAct (EBI)Q5VZR2
FunCoupENSG00000188152
BioGRIDNUTM2G
STRING (EMBL)NUTM2G
ZODIACNUTM2G
Ontologies - Pathways
QuickGOQ5VZR2
Ontology : AmiGO
Ontology : EGO-EBI
NDEx NetworkNUTM2G
Atlas of Cancer Signalling NetworkNUTM2G
Wikipedia pathwaysNUTM2G
Orthology - Evolution
OrthoDB441457
GeneTree (enSembl)ENSG00000188152
Phylogenetic Trees/Animal Genes : TreeFamNUTM2G
HOVERGENQ5VZR2
HOGENOMQ5VZR2
Homologs : HomoloGeneNUTM2G
Homology/Alignments : Family Browser (UCSC)NUTM2G
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerNUTM2G [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)NUTM2G
dbVarNUTM2G
ClinVarNUTM2G
1000_GenomesNUTM2G 
Exome Variant ServerNUTM2G
ExAC (Exome Aggregation Consortium)NUTM2G (select the gene name)
Genetic variants : HAPMAP441457
Genomic Variants (DGV)NUTM2G [DGVbeta]
DECIPHER (Syndromes)9:99691286-99704572  ENSG00000188152
CONAN: Copy Number AnalysisNUTM2G 
Mutations
ICGC Data PortalNUTM2G 
TCGA Data PortalNUTM2G 
Broad Tumor PortalNUTM2G
OASIS PortalNUTM2G [ Somatic mutations - Copy number]
Mutations and Diseases : HGMDNUTM2G
BioMutasearch NUTM2G
DgiDB (Drug Gene Interaction Database)NUTM2G
DoCM (Curated mutations)NUTM2G (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)NUTM2G (select a term)
intoGenNUTM2G
Cancer3DNUTM2G(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenNUTM2G
Genetic Testing Registry NUTM2G
NextProtQ5VZR2 [Medical]
TSGene441457
GENETestsNUTM2G
Huge Navigator NUTM2G [HugePedia]
snp3D : Map Gene to Disease441457
BioCentury BCIQNUTM2G
ClinGenNUTM2G
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD441457
Chemical/Pharm GKB GenePA134899635
Clinical trialNUTM2G
Miscellaneous
canSAR (ICR)NUTM2G (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineNUTM2G
EVEXNUTM2G
GoPubMedNUTM2G
iHOPNUTM2G
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Tue Mar 14 12:35:40 CET 2017

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