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MOSPD2 (motile sperm domain containing 2)

Identity

Alias_symbol (synonym)MGC26706
Other alias-
HGNC (Hugo) MOSPD2
LocusID (NCBI) 158747
Atlas_Id 70380
Location Xp22.2  [Link to chromosome band Xp22]
Location_base_pair Starts at 14885291 and ends at 14921337 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)
MOSPD2 (Xp22.2) / REPS2 (Xp22.2)MOSPD2 (Xp22.2) / SND1 (7q32.1)MOSPD2 (Xp22.2) / TBL1X (Xp22.31)

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)MOSPD2   28381
Cards
Entrez_Gene (NCBI)MOSPD2  158747  motile sperm domain containing 2
Aliases
GeneCards (Weizmann)MOSPD2
Ensembl hg19 (Hinxton)ENSG00000130150 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000130150 [Gene_View]  chrX:14885291-14921337 [Contig_View]  MOSPD2 [Vega]
ICGC DataPortalENSG00000130150
TCGA cBioPortalMOSPD2
AceView (NCBI)MOSPD2
Genatlas (Paris)MOSPD2
WikiGenes158747
SOURCE (Princeton)MOSPD2
Genetics Home Reference (NIH)MOSPD2
Genomic and cartography
GoldenPath hg38 (UCSC)MOSPD2  -     chrX:14885291-14921337 +  Xp22.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MOSPD2  -     Xp22.2   [Description]    (hg19-Feb_2009)
EnsemblMOSPD2 - Xp22.2 [CytoView hg19]  MOSPD2 - Xp22.2 [CytoView hg38]
Mapping of homologs : NCBIMOSPD2 [Mapview hg19]  MOSPD2 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AI744083 AK057941 AK093075 AK315781 AL832230
RefSeq transcript (Entrez)NM_001177475 NM_001330241 NM_152581
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)MOSPD2
Cluster EST : UnigeneHs.744919 [ NCBI ]
CGAP (NCI)Hs.744919
Alternative Splicing GalleryENSG00000130150
Gene ExpressionMOSPD2 [ NCBI-GEO ]   MOSPD2 [ EBI - ARRAY_EXPRESS ]   MOSPD2 [ SEEK ]   MOSPD2 [ MEM ]
Gene Expression Viewer (FireBrowse)MOSPD2 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevestigatorExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)158747
GTEX Portal (Tissue expression)MOSPD2
Human Protein AtlasENSG00000130150-MOSPD2 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ8NHP6   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ8NHP6  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ8NHP6
Splice isoforms : SwissVarQ8NHP6
PhosPhoSitePlusQ8NHP6
Domaine pattern : Prosite (Expaxy)CRAL_TRIO (PS50191)    MSP (PS50202)   
Domains : Interpro (EBI)CRAL-TRIO_dom    CRAL/TRIO_N_dom    MSP_dom    PapD-like   
Domain families : Pfam (Sanger)CRAL_TRIO (PF00650)    Motile_Sperm (PF00635)   
Domain families : Pfam (NCBI)pfam00650    pfam00635   
Domain families : Smart (EMBL)SEC14 (SM00516)  
Conserved Domain (NCBI)MOSPD2
DMDM Disease mutations158747
Blocks (Seattle)MOSPD2
SuperfamilyQ8NHP6
Human Protein Atlas [tissue]ENSG00000130150-MOSPD2 [tissue]
Peptide AtlasQ8NHP6
HPRD06642
IPIIPI00169283   IPI00604606   
Protein Interaction databases
DIP (DOE-UCLA)Q8NHP6
IntAct (EBI)Q8NHP6
FunCoupENSG00000130150
BioGRIDMOSPD2
STRING (EMBL)MOSPD2
ZODIACMOSPD2
Ontologies - Pathways
QuickGOQ8NHP6
Ontology : AmiGOplasma membrane  membrane  integral component of membrane  specific granule membrane  neutrophil degranulation  
Ontology : EGO-EBIplasma membrane  membrane  integral component of membrane  specific granule membrane  neutrophil degranulation  
NDEx NetworkMOSPD2
Atlas of Cancer Signalling NetworkMOSPD2
Wikipedia pathwaysMOSPD2
Orthology - Evolution
OrthoDB158747
GeneTree (enSembl)ENSG00000130150
Phylogenetic Trees/Animal Genes : TreeFamMOSPD2
HOVERGENQ8NHP6
HOGENOMQ8NHP6
Homologs : HomoloGeneMOSPD2
Homology/Alignments : Family Browser (UCSC)MOSPD2
Gene fusions - Rearrangements
Fusion: Tumor Portal MOSPD2
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerMOSPD2 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)MOSPD2
dbVarMOSPD2
ClinVarMOSPD2
1000_GenomesMOSPD2 
Exome Variant ServerMOSPD2
ExAC (Exome Aggregation Consortium)ENSG00000130150
GNOMAD BrowserENSG00000130150
Genetic variants : HAPMAP158747
Genomic Variants (DGV)MOSPD2 [DGVbeta]
DECIPHERMOSPD2 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisMOSPD2 
Mutations
ICGC Data PortalMOSPD2 
TCGA Data PortalMOSPD2 
Broad Tumor PortalMOSPD2
OASIS PortalMOSPD2 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICMOSPD2  [overview]  [genome browser]  [tissue]  [di3trkbution]  
Mutations and Diseases : HGMDMOSPD2
LOVD (Leiden Open Variation Database)Whole genome datasets
LOVD (Leiden Open Variation Database)LOVD - Leiden Open Variation Database
LOVD (Leiden Open Variation Database)LOVD 3.0 shared installation
LOVD (Leiden Open Variation Database)X-chromosome gene database
BioMutasearch MOSPD2
DgiDB (Drug Gene Interaction Database)MOSPD2
DoCM (Curated mutations)MOSPD2 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)MOSPD2 (select a term)
intoGenMOSPD2
Cancer3DMOSPD2(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenMOSPD2
Genetic Testing Registry MOSPD2
NextProtQ8NHP6 [Medical]
TSGene158747
GENETestsMOSPD2
Target ValidationMOSPD2
Huge Navigator MOSPD2 [HugePedia]
snp3D : Map Gene to Disease158747
BioCentury BCIQMOSPD2
ClinGenMOSPD2
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD158747
Chemical/Pharm GKB GenePA134898878
Clinical trialMOSPD2
Miscellaneous
canSAR (ICR)MOSPD2 (select the gene name)
Probes
Litterature
PubMed12 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMOSPD2
EVEXMOSPD2
GoPubMedMOSPD2
iHOPMOSPD2
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Thu Nov 9 12:17:36 CET 2017

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