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

FGFR1OP2 (FGFR1 oncogene partner 2)

Identity

Other namesDKFZp564O1863
HSPC123-like
HGNC FGFR1OP2
Location 12p12.1
Location_base_pair Starts at 26982583 and ends at 27010126 bp from pter (hg18-March_2006).
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
HGNCFGFR1OP2   23098
Entrez_GeneFGFR1OP2  26127  FGFR1 oncogene partner 2
Cards
GeneCardsFGFR1OP2
EnsemblFGFR1OP2 [Search_View]   ENSG00000111790 [Gene_View]
GenatlasFGFR1OP2
GeneLynxFGFR1OP2
eGenomeFGFR1OP2
euGene26127
Genomic and cartography
GoldenPathFGFR1OP2  -  12p12.1   chr12:26982583-27010126 +  12p11.23   [Description]    (hg18-March_2006)
EnsemblFGFR1OP2 - 12p11.23 [CytoView]
NCBIMapview
OMIMDisease map [OMIM]
HomoloGeneFGFR1OP2
Gene and transcription
GenbankAF161472 [ ENTREZ ]
GenbankAK001534 [ ENTREZ ]
GenbankAL117608 [ ENTREZ ]
GenbankAY506561 [ ENTREZ ]
GenbankBC032143 [ ENTREZ ]
RefSeqNM_015633 [ SRS ]    NM_015633 [ ENTREZ ]
RefSeqAC_000055 [ SRS ]    AC_000055 [ ENTREZ ]
RefSeqAC_000144 [ SRS ]    AC_000144 [ ENTREZ ]
RefSeqNC_000012 [ SRS ]    NC_000012 [ ENTREZ ]
RefSeqNT_009714 [ SRS ]    NT_009714 [ ENTREZ ]
RefSeqNW_001838052 [ SRS ]    NW_001838052 [ ENTREZ ]
RefSeqNW_925328 [ SRS ]    NW_925328 [ ENTREZ ]
AceViewFGFR1OP2 AceView - NCBI
UnigeneHs.591162 [ SRS ]    Hs.591162 [ NCBI ]     HS591162 [ spliceNest ]
Fast-db4181 (alternative variants)
Protein : pattern, domain, 3D structure
SwissProtQ9NVK5 [ SRS]    Q9NVK5 [ EXPASY ]     Q9NVK5 [ INTERPRO ]     Q9NVK5 [ UNIPROT ]
InterproIPR008555 DUF837 [ SRS ]    IPR008555 DUF837 [ EBI ]
CluSTrQ9NVK5
PfamPF05769 DUF837 [ SRS ]    PF05769 DUF837 [ Sanger ]    pfam05769 [ NCBI-CDD ]
BlocksQ9NVK5
HPRD10589
Protein Interaction databases
DIPQ9NVK5
IntActQ9NVK5
Polymorphism : SNP, mutations, diseases
OMIM608858    [ map ]   
GENECLINICS608858
SNPFGFR1OP2 [dbSNP-NCBI]  
SNPNM_015633 [SNP-NCI]  
SNPFGFR1OP2 [GeneSNPs - Utah]  FGFR1OP2] [HGBASE - SRS]
HAPMAPFGFR1OP2 [HAPMAP]  
TICdbcytoplasm [Translocation breakpoints In Cancer]  
HGMDFGFR1OP2
General knowledge
Family BrowserFGFR1OP2 [UCSC Family Browser]
SOURCENM_015633
SMDHs.591162
SAGEHs.591162
GOcytoplasm [Amigo]  cytoplasm
PubGeneFGFR1OP2
TreeFamFGFR1OP2
CTD26127 [Comparative ToxicoGenomics Database]
Other databases
Probes
ProbeFGFR1OP2 Related clones (RZPD - Berlin)
PubMed
PubMed4 Pubmed reference(s) in Entrez
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

Search in all EBI   NCBI

Contributor(s)

Written09-2002Dessen P, Le Minor S
Updated03-2008Dessen P

© Atlas of Genetics and Cytogenetics in Oncology and Haematology
indexed on : Sat Oct 11 13:13:13 2008


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

For comments and suggestions or contributions, please contact us

j.l.huret@chu-poitiers.fr.