SHC2 (SHC (Src homology 2 domain containing) transforming protein 2)

Identity

Other names	SCK
	SHCB
	SLI
HGNC	SHC2
Location	19p13.3
Location_base_pair	Starts at 367583 and ends at 411996 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

External links

	Nomenclature
HGNC	SHC2   29869
Entrez_Gene	SHC2  25759  SHC (Src homology 2 domain containing) transforming protein 2
	Cards
GeneCards	SHC2
Ensembl	SHC2 [Search_View]   ENSG00000129946 [Gene_View]
Genatlas	SHC2
GeneLynx	SHC2
eGenome	SHC2
euGene	25759
	Genomic and cartography
GoldenPath	SHC2  -  19p13.3   chr19:367583-411996 -  19p13.3   [Description]    (hg18-March_2006)
Ensembl	SHC2 - 19p13.3 [CytoView]
NCBI	Mapview
OMIM	Disease map [OMIM]
HomoloGene	SHC2
	Gene and transcription
Genbank	AB001451 [ ENTREZ ]
Genbank	AL134433 [ ENTREZ ]
Genbank	AL360254 [ ENTREZ ]
Genbank	BC030527 [ ENTREZ ]
Genbank	BC034544 [ ENTREZ ]
RefSeq	NM_012435 [ SRS ]    NM_012435 [ ENTREZ ]
RefSeq	AC_000062 [ SRS ]    AC_000062 [ ENTREZ ]
RefSeq	AC_000151 [ SRS ]    AC_000151 [ ENTREZ ]
RefSeq	NC_000019 [ SRS ]    NC_000019 [ ENTREZ ]
RefSeq	NT_011255 [ SRS ]    NT_011255 [ ENTREZ ]
RefSeq	NW_001838476 [ SRS ]    NW_001838476 [ ENTREZ ]
RefSeq	NW_927140 [ SRS ]    NW_927140 [ ENTREZ ]
AceView	SHC2 AceView - NCBI
Unigene	Hs.30965 [ SRS ]    Hs.30965 [ NCBI ]     HS30965 [ spliceNest ]
Fast-db	436 (alternative variants)
	Protein : pattern, domain, 3D structure
SwissProt	P98077 [ SRS]    P98077 [ EXPASY ]     P98077 [ INTERPRO ]     P98077 [ UNIPROT ]
Prosite	PS01179 PID [ SRS ]    PS01179 PID [ Expasy ]
Prosite	PS50001 SH2 [ SRS ]    PS50001 SH2 [ Expasy ]
CluSTr	P98077
Smart	SM00462 PTB [EMBL]
Smart	SM00252 SH2 [EMBL]
Prodom	PD000093 SH2[INRA-Toulouse]
Prodom	P98077 SHC2_HUMAN [ Domain structure ]   P98077 SHC2_HUMAN  [ sequences sharing at least 1 domain ]
Blocks	P98077
	Protein Interaction databases
DIP	P98077
IntAct	P98077
	Polymorphism : SNP, mutations, diseases
OMIM	605217    [ map ]
GENECLINICS	605217
SNP	SHC2 [dbSNP-NCBI]
SNP	NM_012435 [SNP-NCI]
SNP	SHC2 [GeneSNPs - Utah]  SHC2] [HGBASE - SRS]
HAPMAP	SHC2 [HAPMAP]
COSMIC	SHC2 [Somatic mutation (COSMIC-CGP-Sanger)]
HGMD	SHC2
	General knowledge
Family Browser	SHC2 [UCSC Family Browser]
SOURCE	NM_012435
SMD	Hs.30965
SAGE	Hs.30965
GO	protein binding [Amigo]  protein binding
GO	cellular_component [Amigo]  cellular_component
GO	intracellular signaling cascade [Amigo]  intracellular signaling cascade
GO	Ras protein signal transduction [Amigo]  Ras protein signal transduction
KEGG	VEGF signaling pathway
KEGG	Focal adhesion
KEGG	Natural killer cell mediated cytotoxicity
KEGG	Insulin signaling pathway
PubGene	SHC2
TreeFam	SHC2
CTD	25759 [Comparative ToxicoGenomics Database]
	Other databases
	Probes
Probe	SHC2 Related clones (RZPD - Berlin)
	PubMed
PubMed	9 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 13:32:08 2008