Atlas of Genetics and Cytogenetics in Oncology and Haematology

Home   Genes   Leukemias   Solid Tumors   Cancer-Prone   Deep Insight   Case Reports   Journals  Portal   Teaching   
X Y 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 NA

ANKRD42 (ankyrin repeat domain 42)

Identity

Alias (NCBI)PPP1R79
SARP
HGNC (Hugo) ANKRD42
HGNC Alias symbFLJ37874
SARP
PPP1R79
HGNC Alias nameprotein phosphatase 1, regulatory subunit 79
LocusID (NCBI) 338699
Atlas_Id 60351
Location 11q14.1  [Link to chromosome band 11q14]
Location_base_pair Starts at 83193739 and ends at 83248971 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)
ADIPOR2 (12p13.33) / ANKRD42 (11q14.1)ANKRD42 (11q14.1) / RHOD (11q13.2)SRPK1 (6p21.31) / ANKRD42 (11q14.1)

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

 

Other Solid tumors implicated (Data extracted from papers in the Atlas) [ 2 ]
  t(6;11)(p21;q14) SRPK1/ANKRD42
t(11;11)(q13;q14) ANKRD42/RHOD

External links

Nomenclature
HGNC (Hugo)ANKRD42   26752
Cards
Entrez_Gene (NCBI)ANKRD42  338699  ankyrin repeat domain 42
AliasesPPP1R79; SARP
GeneCards (Weizmann)ANKRD42
Ensembl hg19 (Hinxton)ENSG00000137494 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000137494 [Gene_View]  ENSG00000137494 [Sequence]  chr11:83193739-83248971 [Contig_View]  ANKRD42 [Vega]
ICGC DataPortalENSG00000137494
TCGA cBioPortalANKRD42
AceView (NCBI)ANKRD42
Genatlas (Paris)ANKRD42
WikiGenes338699
SOURCE (Princeton)ANKRD42
Genetics Home Reference (NIH)ANKRD42
Genomic and cartography
GoldenPath hg38 (UCSC)ANKRD42  -     chr11:83193739-83248971 +  11q14.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)ANKRD42  -     11q14.1   [Description]    (hg19-Feb_2009)
GoldenPathANKRD42 - 11q14.1 [CytoView hg19]  ANKRD42 - 11q14.1 [CytoView hg38]
ImmunoBaseENSG00000137494
genome Data Viewer NCBIANKRD42 [Mapview hg19]  
Gene and transcription
Genbank (Entrez)AK095193 AK310765 BC045621 BC062729 BC171752
RefSeq transcript (Entrez)NM_001300972 NM_001300973 NM_001300975 NM_001300976 NM_001300977 NM_182603
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)ANKRD42
Alternative Splicing GalleryENSG00000137494
Gene ExpressionANKRD42 [ NCBI-GEO ]   ANKRD42 [ EBI - ARRAY_EXPRESS ]   ANKRD42 [ SEEK ]   ANKRD42 [ MEM ]
Gene Expression Viewer (FireBrowse)ANKRD42 [ Firebrowse - Broad ]
GenevisibleExpression of ANKRD42 in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)338699
GTEX Portal (Tissue expression)ANKRD42
Human Protein AtlasENSG00000137494-ANKRD42 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ8N9B4   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ8N9B4  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ8N9B4
Splice isoforms : SwissVarQ8N9B4
PhosPhoSitePlusQ8N9B4
Domaine pattern : Prosite (Expaxy)ANK_REP_REGION (PS50297)    ANK_REPEAT (PS50088)   
Domains : Interpro (EBI)Ankyrin_rpt    Ankyrin_rpt-contain_dom    Ankyrin_rpt-contain_sf    EF_Hand_1_Ca_BS   
Domain families : Pfam (Sanger)Ank_2 (PF12796)   
Domain families : Pfam (NCBI)pfam12796   
Domain families : Smart (EMBL)ANK (SM00248)  
Conserved Domain (NCBI)ANKRD42
DMDM Disease mutations338699
Blocks (Seattle)ANKRD42
SuperfamilyQ8N9B4
Human Protein Atlas [tissue]ENSG00000137494-ANKRD42 [tissue]
Peptide AtlasQ8N9B4
HPRD08230
IPIIPI00298502   IPI00760686   IPI00984556   IPI00872928   IPI00977606   IPI00983224   IPI00976948   IPI00976443   
Protein Interaction databases
DIP (DOE-UCLA)Q8N9B4
IntAct (EBI)Q8N9B4
FunCoupENSG00000137494
BioGRIDANKRD42
STRING (EMBL)ANKRD42
ZODIACANKRD42
Ontologies - Pathways
QuickGOQ8N9B4
Ontology : AmiGO
Ontology : EGO-EBI
NDEx NetworkANKRD42
Atlas of Cancer Signalling NetworkANKRD42
Wikipedia pathwaysANKRD42
Orthology - Evolution
OrthoDB338699
GeneTree (enSembl)ENSG00000137494
Phylogenetic Trees/Animal Genes : TreeFamANKRD42
HOGENOMQ8N9B4
Homologs : HomoloGeneANKRD42
Homology/Alignments : Family Browser (UCSC)ANKRD42
Gene fusions - Rearrangements
Fusion : QuiverANKRD42
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerANKRD42 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)ANKRD42
dbVarANKRD42
ClinVarANKRD42
1000_GenomesANKRD42 
Exome Variant ServerANKRD42
GNOMAD BrowserENSG00000137494
Varsome BrowserANKRD42
Genetic variants : HAPMAP338699
Genomic Variants (DGV)ANKRD42 [DGVbeta]
DECIPHERANKRD42 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisANKRD42 
Mutations
ICGC Data PortalANKRD42 
TCGA Data PortalANKRD42 
Broad Tumor PortalANKRD42
OASIS PortalANKRD42 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICANKRD42  [overview]  [genome browser]  [tissue]  [distribution]  
Somatic Mutations in Cancer : COSMIC3DANKRD42
Mutations and Diseases : HGMDANKRD42
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
BioMutasearch ANKRD42
DgiDB (Drug Gene Interaction Database)ANKRD42
DoCM (Curated mutations)ANKRD42 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)ANKRD42 (select a term)
intoGenANKRD42
Cancer3DANKRD42(select the gene name)
Impact of mutations[PolyPhen2] [Provean] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
DisGeNETANKRD42
MedgenANKRD42
Genetic Testing Registry ANKRD42
NextProtQ8N9B4 [Medical]
TSGene338699
GENETestsANKRD42
Target ValidationANKRD42
Huge Navigator ANKRD42 [HugePedia]
snp3D : Map Gene to Disease338699
BioCentury BCIQANKRD42
ClinGenANKRD42
Clinical trials, drugs, therapy
Protein Interactions : CTD338699
Pharm GKB GenePA142672609
Clinical trialANKRD42
Miscellaneous
canSAR (ICR)ANKRD42 (select the gene name)
HarmonizomeANKRD42
DataMed IndexANKRD42
Probes
Litterature
PubMed8 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineANKRD42
EVEXANKRD42
GoPubMedANKRD42
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

Search in all EBI   NCBI

© Atlas of Genetics and Cytogenetics in Oncology and Haematology
indexed on : Thu Jul 16 15:47:37 CEST 2020
Home   Genes   Leukemias   Solid Tumors   Cancer-Prone   Deep Insight   Case Reports   Journals  Portal   Teaching   

For comments and suggestions or contributions, please contact us

jlhuret@AtlasGeneticsOncology.org.