C10orf97 (chromosome 10 open reading frame 97)

Identity

Other names	CARP
	DERP5
	FLJ13397
	MST126
	MSTP126
	RP11-394I23.1
	my042
HGNC	C10orf97
Location	10p13
Location_base_pair	Starts at 15860181 and ends at 15942525 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
HGNC	C10orf97   23578
Entrez_Gene	C10orf97  80013  chromosome 10 open reading frame 97
	Cards
GeneCards	C10orf97
Ensembl	C10orf97 [Search_View]   ENSG00000148481 [Gene_View]
Genatlas	C10orf97
GeneLynx	C10orf97
eGenome	C10orf97
euGene	80013
	Genomic and cartography
GoldenPath	C10orf97  -  10p13   chr10:15860181-15942525 -  10p13   [Description]    (hg18-March_2006)
Ensembl	C10orf97 - 10p13 [CytoView]
NCBI	Mapview
OMIM	Disease map [OMIM]
HomoloGene	C10orf97
	Gene and transcription
Genbank	AB014761 [ ENTREZ ]
Genbank	AF063600 [ ENTREZ ]
Genbank	AF176916 [ ENTREZ ]
Genbank	AK023459 [ ENTREZ ]
Genbank	AL833873 [ ENTREZ ]
RefSeq	NM_024948 [ SRS ]    NM_024948 [ ENTREZ ]
RefSeq	AC_000053 [ SRS ]    AC_000053 [ ENTREZ ]
RefSeq	AC_000142 [ SRS ]    AC_000142 [ ENTREZ ]
RefSeq	NC_000010 [ SRS ]    NC_000010 [ ENTREZ ]
RefSeq	NT_077569 [ SRS ]    NT_077569 [ ENTREZ ]
RefSeq	NW_001837931 [ SRS ]    NW_001837931 [ ENTREZ ]
RefSeq	NW_924584 [ SRS ]    NW_924584 [ ENTREZ ]
AceView	C10orf97 AceView - NCBI
Unigene	Hs.590985 [ SRS ]    Hs.590985 [ NCBI ]     HS590985 [ spliceNest ]
Fast-db	3817 (alternative variants)
	Protein : pattern, domain, 3D structure
SwissProt	Q9H8M7 [ SRS]    Q9H8M7 [ EXPASY ]     Q9H8M7 [ INTERPRO ]     Q9H8M7 [ UNIPROT ]
Interpro	IPR011992 EF-Hand_type [ SRS ]    IPR011992 EF-Hand_type [ EBI ]
CluSTr	Q9H8M7
Prodom	PD000012 EF-hand[INRA-Toulouse]
Prodom	Q9H8M7 CARP_HUMAN [ Domain structure ]   Q9H8M7 CARP_HUMAN  [ sequences sharing at least 1 domain ]
Blocks	Q9H8M7
HPRD	10702
	Protein Interaction databases
DIP	Q9H8M7
IntAct	Q9H8M7
	Polymorphism : SNP, mutations, diseases
OMIM	611649    [ map ]
GENECLINICS	611649
SNP	C10orf97 [dbSNP-NCBI]
SNP	NM_024948 [SNP-NCI]
SNP	C10orf97 [GeneSNPs - Utah]  C10orf97] [HGBASE - SRS]
HAPMAP	C10orf97 [HAPMAP]
COSMIC	C10orf97 [Somatic mutation (COSMIC-CGP-Sanger)]
HGMD	C10orf97
	General knowledge
Family Browser	C10orf97 [UCSC Family Browser]
SOURCE	NM_024948
SMD	Hs.590985
SAGE	Hs.590985
GO	calcium ion binding [Amigo]  calcium ion binding
GO	nucleus [Amigo]  nucleus
GO	apoptosis [Amigo]  apoptosis
PubGene	C10orf97
TreeFam	C10orf97
CTD	80013 [Comparative ToxicoGenomics Database]
	Other databases
	Probes
Probe	C10orf97 Related clones (RZPD - Berlin)
	PubMed
PubMed	3 Pubmed reference(s) in Entrez

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
Updated	03-2008	Dessen P

© Atlas of Genetics and Cytogenetics in Oncology and Haematology

indexed on : Sat Oct 11 13:05:14 2008