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MRFAP1L1 (Morf4 family associated protein 1 like 1)

Identity

Alias_symbol (synonym)MGC9651
Other aliasPP784
HGNC (Hugo) MRFAP1L1
LocusID (NCBI) 114932
Atlas_Id 70408
Location 4p16.1  [Link to chromosome band 4p16]
Location_base_pair Starts at 6707701 and ends at 6709879 bp from pter ( according to hg38-Dec_2013)

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)MRFAP1L1   28796
Cards
Entrez_Gene (NCBI)MRFAP1L1  114932  Morf4 family associated protein 1 like 1
AliasesPP784
GeneCards (Weizmann)MRFAP1L1
Ensembl hg19 (Hinxton)ENSG00000178988 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000178988 [Gene_View]  chr4:6707701-6709879 [Contig_View]  MRFAP1L1 [Vega]
ICGC DataPortalENSG00000178988
TCGA cBioPortalMRFAP1L1
AceView (NCBI)MRFAP1L1
Genatlas (Paris)MRFAP1L1
WikiGenes114932
SOURCE (Princeton)MRFAP1L1
Genetics Home Reference (NIH)MRFAP1L1
Genomic and cartography
GoldenPath hg38 (UCSC)MRFAP1L1  -     chr4:6707701-6709879 -  4p16.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MRFAP1L1  -     4p16.1   [Description]    (hg19-Feb_2009)
EnsemblMRFAP1L1 - 4p16.1 [CytoView hg19]  MRFAP1L1 - 4p16.1 [CytoView hg38]
Mapping of homologs : NCBIMRFAP1L1 [Mapview hg19]  MRFAP1L1 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AF155654 AF258591 AK312676 BC008087 BC066897
RefSeq transcript (Entrez)NM_152301 NM_203462
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)MRFAP1L1
Cluster EST : UnigeneHs.593159 [ NCBI ]
CGAP (NCI)Hs.593159
Alternative Splicing GalleryENSG00000178988
Gene ExpressionMRFAP1L1 [ NCBI-GEO ]   MRFAP1L1 [ EBI - ARRAY_EXPRESS ]   MRFAP1L1 [ SEEK ]   MRFAP1L1 [ MEM ]
Gene Expression Viewer (FireBrowse)MRFAP1L1 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)114932
GTEX Portal (Tissue expression)MRFAP1L1
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ96HT8   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ96HT8  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ96HT8
Splice isoforms : SwissVarQ96HT8
PhosPhoSitePlusQ96HT8
Domains : Interpro (EBI)MRFAP1   
Domain families : Pfam (Sanger)MRFAP1 (PF15155)   
Domain families : Pfam (NCBI)pfam15155   
Conserved Domain (NCBI)MRFAP1L1
DMDM Disease mutations114932
Blocks (Seattle)MRFAP1L1
SuperfamilyQ96HT8
Human Protein AtlasENSG00000178988
Peptide AtlasQ96HT8
HPRD15162
IPIIPI00095951   
Protein Interaction databases
DIP (DOE-UCLA)Q96HT8
IntAct (EBI)Q96HT8
FunCoupENSG00000178988
BioGRIDMRFAP1L1
STRING (EMBL)MRFAP1L1
ZODIACMRFAP1L1
Ontologies - Pathways
QuickGOQ96HT8
Ontology : AmiGOprotein binding  identical protein binding  
Ontology : EGO-EBIprotein binding  identical protein binding  
NDEx NetworkMRFAP1L1
Atlas of Cancer Signalling NetworkMRFAP1L1
Wikipedia pathwaysMRFAP1L1
Orthology - Evolution
OrthoDB114932
GeneTree (enSembl)ENSG00000178988
Phylogenetic Trees/Animal Genes : TreeFamMRFAP1L1
HOVERGENQ96HT8
HOGENOMQ96HT8
Homologs : HomoloGeneMRFAP1L1
Homology/Alignments : Family Browser (UCSC)MRFAP1L1
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerMRFAP1L1 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)MRFAP1L1
dbVarMRFAP1L1
ClinVarMRFAP1L1
1000_GenomesMRFAP1L1 
Exome Variant ServerMRFAP1L1
ExAC (Exome Aggregation Consortium)MRFAP1L1 (select the gene name)
Genetic variants : HAPMAP114932
Genomic Variants (DGV)MRFAP1L1 [DGVbeta]
DECIPHERMRFAP1L1 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisMRFAP1L1 
Mutations
ICGC Data PortalMRFAP1L1 
TCGA Data PortalMRFAP1L1 
Broad Tumor PortalMRFAP1L1
OASIS PortalMRFAP1L1 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICMRFAP1L1  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDMRFAP1L1
LOVD (Leiden Open Variation Database)Whole genome datasets
LOVD (Leiden Open Variation Database)LOVD 3.0 shared installation
BioMutasearch MRFAP1L1
DgiDB (Drug Gene Interaction Database)MRFAP1L1
DoCM (Curated mutations)MRFAP1L1 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)MRFAP1L1 (select a term)
intoGenMRFAP1L1
Cancer3DMRFAP1L1(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenMRFAP1L1
Genetic Testing Registry MRFAP1L1
NextProtQ96HT8 [Medical]
TSGene114932
GENETestsMRFAP1L1
Target ValidationMRFAP1L1
Huge Navigator MRFAP1L1 [HugePedia]
snp3D : Map Gene to Disease114932
BioCentury BCIQMRFAP1L1
ClinGenMRFAP1L1
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD114932
Chemical/Pharm GKB GenePA142671333
Clinical trialMRFAP1L1
Miscellaneous
canSAR (ICR)MRFAP1L1 (select the gene name)
Probes
Litterature
PubMed9 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMRFAP1L1
EVEXMRFAP1L1
GoPubMedMRFAP1L1
iHOPMRFAP1L1
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Wed May 31 15:31:20 CEST 2017

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