Atlas of Genetics and Cytogenetics in Oncology and Haematology


Home   Genes   Leukemias   Solid Tumours   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

FAM86HP (family with sequence similarity 86, member A pseudogene)

Identity

Alias_namesfamily with sequence similarity 86, member H, pseudogene
Other alias-
HGNC (Hugo) FAM86HP
LocusID (NCBI) 729375
Atlas_Id 63266
Location 3q22.1  [Link to chromosome band 3q22]
Location_base_pair Starts at 129816625 and ends at 129830276 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)FAM86HP   42359
Cards
Entrez_Gene (NCBI)FAM86HP  729375  family with sequence similarity 86, member A pseudogene
Aliases
GeneCards (Weizmann)FAM86HP
Ensembl hg19 (Hinxton) [Gene_View]  chr3:129816625-129830276 [Contig_View]  FAM86HP [Vega]
Ensembl hg38 (Hinxton) [Gene_View]  chr3:129816625-129830276 [Contig_View]  FAM86HP [Vega]
TCGA cBioPortalFAM86HP
AceView (NCBI)FAM86HP
Genatlas (Paris)FAM86HP
WikiGenes729375
SOURCE (Princeton)FAM86HP
Genetics Home Reference (NIH)FAM86HP
Genomic and cartography
GoldenPath hg19 (UCSC)FAM86HP  -     chr3:129816625-129830276 -  3q22.1   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)FAM86HP  -     3q22.1   [Description]    (hg38-Dec_2013)
EnsemblFAM86HP - 3q22.1 [CytoView hg19]  FAM86HP - 3q22.1 [CytoView hg38]
Mapping of homologs : NCBIFAM86HP [Mapview hg19]  FAM86HP [Mapview hg38]
Gene and transcription
Genbank (Entrez)AK124448 DA296336
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)NC_000003 NC_018914 NT_005612 NW_004929311
Consensus coding sequences : CCDS (NCBI)FAM86HP
Cluster EST : UnigeneHs.123633 [ NCBI ]
CGAP (NCI)Hs.123633
Gene ExpressionFAM86HP [ NCBI-GEO ]   FAM86HP [ EBI - ARRAY_EXPRESS ]   FAM86HP [ SEEK ]   FAM86HP [ MEM ]
Gene Expression Viewer (FireBrowse)FAM86HP [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)729375
GTEX Portal (Tissue expression)FAM86HP
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)FAM86HP
DMDM Disease mutations729375
Blocks (Seattle)FAM86HP
Protein Interaction databases
BioGRIDFAM86HP
STRING (EMBL)FAM86HP
ZODIACFAM86HP
Ontologies - Pathways
Huge Navigator FAM86HP [HugePedia]
snp3D : Map Gene to Disease729375
BioCentury BCIQFAM86HP
ClinGenFAM86HP
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD729375
Clinical trialFAM86HP
Miscellaneous
canSAR (ICR)FAM86HP (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineFAM86HP
EVEXFAM86HP
GoPubMedFAM86HP
iHOPFAM86HP
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 : Tue Mar 14 12:04:24 CET 2017

Home   Genes   Leukemias   Solid Tumours   Cancer-Prone   Deep Insight   Case Reports   Journals  Portal   Teaching   

For comments and suggestions or contributions, please contact us

jlhuret@AtlasGeneticsOncology.org.