REPS2 (RALBP1 associated Eps domain containing 2)

Identity

Other names	POB1
Hugo	REPS2
Location	Xp22.2
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
Hugo	REPS2
GDB	REPS2
Entrez_Gene	REPS2  9185  RALBP1 associated Eps domain containing 2
	Cards
GeneCards	REPS2
Ensembl	REPS2 [Search_View]   ENSG00000169891 [Gene_View]
Genatlas	REPS2
GeneLynx	REPS2
eGenome	REPS2
euGene	9185
	Genomic and cartography
GoldenPath	REPS2  -  Xp22.2   chrX:16874735-17081324 +  Xp22.2   [Description]    (hg18-March_2006)
Ensembl	REPS2 - Xp22.2 [CytoView]
NCBI	Mapview
OMIM	Disease map [OMIM]
HomoloGene	REPS2
	Gene and transcription
Genbank	AB208937 [ ENTREZ ]
Genbank	AF010233 [ ENTREZ ]
Genbank	AF511533 [ ENTREZ ]
Genbank	AF512951 [ ENTREZ ]
Genbank	AI221053 [ ENTREZ ]
RefSeq	NM_001080975 [ SRS ]    NM_001080975 [ ENTREZ ]
RefSeq	NM_004726 [ SRS ]    NM_004726 [ ENTREZ ]
RefSeq	AC_000066 [ SRS ]    AC_000066 [ ENTREZ ]
RefSeq	NC_000023 [ SRS ]    NC_000023 [ ENTREZ ]
RefSeq	NT_011757 [ SRS ]    NT_011757 [ ENTREZ ]
RefSeq	NW_927700 [ SRS ]    NW_927700 [ ENTREZ ]
AceView	REPS2 AceView - NCBI
Unigene	Hs.186810 [ SRS ]    Hs.186810 [ NCBI ]     HS186810 [ spliceNest ]
Fast-db	2651 (alternative variants)
	Protein : pattern, domain, 3D structure
SwissProt	Q8NFH8 [ SRS]    Q8NFH8 [ EXPASY ]     Q8NFH8 [ INTERPRO ]
Prosite	PS00018 EF_HAND_1 [ SRS ]    PS00018 EF_HAND_1 [ Expasy ]
Prosite	PS50222 EF_HAND_2 [ SRS ]    PS50222 EF_HAND_2 [ Expasy ]
Prosite	PS50031 EH [ SRS ]    PS50031 EH [ Expasy ]
Interpro	IPR011992 EF-Hand_type [ SRS ]    IPR011992 EF-Hand_type [ EBI ]
Interpro	IPR002048 EF_hand_Ca_bd [ SRS ]    IPR002048 EF_hand_Ca_bd [ EBI ]
Interpro	IPR000261 EPS15_homology [ SRS ]    IPR000261 EPS15_homology [ EBI ]
CluSTr	Q8NFH8
Smart	SM00027 EH [EMBL]
Blocks	Q8NFH8
PDB	1IQ3 [ SRS ]    1IQ3 [ PdbSum ],   1IQ3 [ IMB ]   1IQ3 [ RSDB ]
HPRD	02262
	Protein Interaction databases
DIP	Q8NFH8
IntAct	Q8NFH8
	Polymorphism : SNP, mutations, diseases
OMIM	300317    [ map ]
GENECLINICS	300317
SNP	REPS2 [dbSNP-NCBI]
SNP	NM_001080975 [SNP-NCI]
SNP	NM_004726 [SNP-NCI]
SNP	REPS2 [GeneSNPs - Utah]  REPS2] [HGBASE - SRS]
HAPMAP	REPS2 [HAPMAP]
COSMIC	REPS2 [Somatic mutation (COSMIC-CGP-Sanger)]
HGMD	REPS2
	General knowledge
Family Browser	REPS2 [UCSC Family Browser]
SOURCE	NM_001080975
SOURCE	NM_004726
SMD	Hs.186810
SAGE	Hs.186810
GO	calcium ion binding [Amigo]  calcium ion binding
GO	calcium ion binding [Amigo]  calcium ion binding
GO	protein binding [Amigo]  protein binding
GO	cytoplasm [Amigo]  cytoplasm
GO	protein complex assembly [Amigo]  protein complex assembly
GO	epidermal growth factor receptor signaling pathway [Amigo]  epidermal growth factor receptor signaling pathway
PubGene	REPS2
TreeFam	REPS2
CTD	9185 [Comparative Genomics Database]
	Other databases
	Probes
Probe	REPS2 Related clones (RZPD - Berlin)
	PubMed
PubMed	12 Pubmed reference(s) in LocusLink

Genes in title	automatic search in PubMed
REVIEW articles	automatic search in PubMed
Last year publications	automatic search in PubMed

Search in all EBI   NCBI

Contributor(s)

Written	09-2002	Dessen P, Le Minor S

© Atlas of Genetics and Cytogenetics in Oncology and Haematology

indexed on : Thu May 22 20:25:49 2008