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MUM1L1 (melanoma associated antigen (mutated) 1-like 1)

Identity

Alias_namesmelanoma associated antigen (mutated) 1-like 1
Alias_symbol (synonym)FLJ33516
Other alias-
HGNC (Hugo) MUM1L1
LocusID (NCBI) 139221
Atlas_Id 42943
Location Xq22.3  [Link to chromosome band Xq22]
Location_base_pair Starts at 105412298 and ends at 105452949 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)MUM1L1   26583
Cards
Entrez_Gene (NCBI)MUM1L1  139221  melanoma associated antigen (mutated) 1-like 1
Aliases
GeneCards (Weizmann)MUM1L1
Ensembl hg19 (Hinxton)ENSG00000157502 [Gene_View]  chrX:105412298-105452949 [Contig_View]  MUM1L1 [Vega]
Ensembl hg38 (Hinxton)ENSG00000157502 [Gene_View]  chrX:105412298-105452949 [Contig_View]  MUM1L1 [Vega]
ICGC DataPortalENSG00000157502
TCGA cBioPortalMUM1L1
AceView (NCBI)MUM1L1
Genatlas (Paris)MUM1L1
WikiGenes139221
SOURCE (Princeton)MUM1L1
Genetics Home Reference (NIH)MUM1L1
Genomic and cartography
GoldenPath hg19 (UCSC)MUM1L1  -     chrX:105412298-105452949 +  Xq22.3   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)MUM1L1  -     Xq22.3   [Description]    (hg38-Dec_2013)
EnsemblMUM1L1 - Xq22.3 [CytoView hg19]  MUM1L1 - Xq22.3 [CytoView hg38]
Mapping of homologs : NCBIMUM1L1 [Mapview hg19]  MUM1L1 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AA412505 AK056478 AK090835 BC031229 BC109292
RefSeq transcript (Entrez)NM_001171020 NM_152423
RefSeq genomic (Entrez)NC_000023 NC_018934 NG_016639 NT_011651 NW_004929444
Consensus coding sequences : CCDS (NCBI)MUM1L1
Cluster EST : UnigeneHs.592221 [ NCBI ]
CGAP (NCI)Hs.592221
Alternative Splicing GalleryENSG00000157502
Gene ExpressionMUM1L1 [ NCBI-GEO ]   MUM1L1 [ EBI - ARRAY_EXPRESS ]   MUM1L1 [ SEEK ]   MUM1L1 [ MEM ]
Gene Expression Viewer (FireBrowse)MUM1L1 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)139221
GTEX Portal (Tissue expression)MUM1L1
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ5H9M0   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ5H9M0  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ5H9M0
Splice isoforms : SwissVarQ5H9M0
PhosPhoSitePlusQ5H9M0
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MUM1L1
DMDM Disease mutations139221
Blocks (Seattle)MUM1L1
SuperfamilyQ5H9M0
Human Protein AtlasENSG00000157502
Peptide AtlasQ5H9M0
HPRD06555
IPIIPI00383970   
Protein Interaction databases
DIP (DOE-UCLA)Q5H9M0
IntAct (EBI)Q5H9M0
FunCoupENSG00000157502
BioGRIDMUM1L1
STRING (EMBL)MUM1L1
ZODIACMUM1L1
Ontologies - Pathways
QuickGOQ5H9M0
Ontology : AmiGOextracellular exosome  
Ontology : EGO-EBIextracellular exosome  
NDEx NetworkMUM1L1
Atlas of Cancer Signalling NetworkMUM1L1
Wikipedia pathwaysMUM1L1
Orthology - Evolution
OrthoDB139221
GeneTree (enSembl)ENSG00000157502
Phylogenetic Trees/Animal Genes : TreeFamMUM1L1
HOVERGENQ5H9M0
HOGENOMQ5H9M0
Homologs : HomoloGeneMUM1L1
Homology/Alignments : Family Browser (UCSC)MUM1L1
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerMUM1L1 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)MUM1L1
dbVarMUM1L1
ClinVarMUM1L1
1000_GenomesMUM1L1 
Exome Variant ServerMUM1L1
ExAC (Exome Aggregation Consortium)MUM1L1 (select the gene name)
Genetic variants : HAPMAP139221
Genomic Variants (DGV)MUM1L1 [DGVbeta]
DECIPHER (Syndromes)X:105412298-105452949  ENSG00000157502
CONAN: Copy Number AnalysisMUM1L1 
Mutations
ICGC Data PortalMUM1L1 
TCGA Data PortalMUM1L1 
Broad Tumor PortalMUM1L1
OASIS PortalMUM1L1 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICMUM1L1  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDMUM1L1
LOVD (Leiden Open Variation Database)Whole genome datasets
LOVD (Leiden Open Variation Database)LOVD 3.0 shared installation
LOVD (Leiden Open Variation Database)X-chromosome gene database
BioMutasearch MUM1L1
DgiDB (Drug Gene Interaction Database)MUM1L1
DoCM (Curated mutations)MUM1L1 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)MUM1L1 (select a term)
intoGenMUM1L1
Cancer3DMUM1L1(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenMUM1L1
Genetic Testing Registry MUM1L1
NextProtQ5H9M0 [Medical]
TSGene139221
GENETestsMUM1L1
Huge Navigator MUM1L1 [HugePedia]
snp3D : Map Gene to Disease139221
BioCentury BCIQMUM1L1
ClinGenMUM1L1
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD139221
Chemical/Pharm GKB GenePA134880222
Clinical trialMUM1L1
Miscellaneous
canSAR (ICR)MUM1L1 (select the gene name)
Probes
Litterature
PubMed8 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMUM1L1
EVEXMUM1L1
GoPubMedMUM1L1
iHOPMUM1L1
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 13:17:43 CET 2017

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