ID1 (inhibitor of DNA binding 1, dominant negative helix-loop-helix protein)

Identity

Other names	ID
HGNC	ID1
Location	20q11
Location_base_pair	Starts at 29656753 and ends at 29657974 bp from pter ( according to 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	ID1   5360
Entrez_Gene	ID1  3397  inhibitor of DNA binding 1, dominant negative helix-loop-helix protein
	Cards
GeneCards	ID1
Ensembl	ID1 [Search_View]   ENSG00000125968 [Gene_View]
Genatlas	ID1
GeneLynx	ID1
eGenome	ID1
euGene	3397
	Genomic and cartography
GoldenPath	ID1  -  20q11   chr20:29656753-29657974 +  20q11.21   [Description]    (hg18-March_2006)
Ensembl	ID1 - 20q11.21 [CytoView]
NCBI	Mapview
OMIM	Disease map [OMIM]
HomoloGene	ID1
	Gene and transcription
Genbank	AK291152 [ ENTREZ ]
Genbank	BC000613 [ ENTREZ ]
Genbank	BC012420 [ ENTREZ ]
Genbank	BG546814 [ ENTREZ ]
Genbank	BT007443 [ ENTREZ ]
RefSeq	NM_002165 [ SRS ]    NM_002165 [ ENTREZ ]
RefSeq	NM_181353 [ SRS ]    NM_181353 [ ENTREZ ]
RefSeq	AC_000063 [ SRS ]    AC_000063 [ ENTREZ ]
RefSeq	AC_000152 [ SRS ]    AC_000152 [ ENTREZ ]
RefSeq	NC_000020 [ SRS ]    NC_000020 [ ENTREZ ]
RefSeq	NT_028392 [ SRS ]    NT_028392 [ ENTREZ ]
RefSeq	NW_001838664 [ SRS ]    NW_001838664 [ ENTREZ ]
RefSeq	NW_927339 [ SRS ]    NW_927339 [ ENTREZ ]
AceView	ID1 AceView - NCBI
Unigene	Hs.504609 [ SRS ]    Hs.504609 [ NCBI ]     HS504609 [ spliceNest ]
Fast-db	7606 (alternative variants)
	Protein : pattern, domain, 3D structure
SwissProt	P41134 [ SRS]    P41134 [ EXPASY ]     P41134 [ INTERPRO ]     P41134 [ UNIPROT ]
Prosite	PS50888 HLH [ SRS ]    PS50888 HLH [ Expasy ]
Interpro	IPR001092 HLH_basic [ SRS ]    IPR001092 HLH_basic [ EBI ]
Interpro	IPR011598 HLH_DNA_bd [ SRS ]    IPR011598 HLH_DNA_bd [ EBI ]
CluSTr	P41134
Pfam	PF00010 HLH [ SRS ]    PF00010 HLH [ Sanger ]    pfam00010 [ NCBI-CDD ]
Smart	SM00353 HLH [EMBL]
Blocks	P41134
HPRD	08980
	Protein Interaction databases
DIP	P41134
IntAct	P41134
	Polymorphism : SNP, mutations, diseases
OMIM	600349    [ map ]
GENECLINICS	600349
SNP	ID1 [dbSNP-NCBI]
SNP	NM_002165 [SNP-NCI]
SNP	NM_181353 [SNP-NCI]
SNP	ID1 [GeneSNPs - Utah]  ID1] [HGBASE - SRS]
HAPMAP	ID1 [HAPMAP]
COSMIC	ID1 [Somatic mutation (COSMIC-CGP-Sanger)]
HGMD	ID1
	General knowledge
Family Browser	ID1 [UCSC Family Browser]
SOURCE	NM_002165
SOURCE	NM_181353
SMD	Hs.504609
SAGE	Hs.504609
GO	protein binding [Amigo]  protein binding
GO	nucleus [Amigo]  nucleus
GO	multicellular organismal development [Amigo]  multicellular organismal development
GO	transcription regulator activity [Amigo]  transcription regulator activity
GO	regulation of transcription [Amigo]  regulation of transcription
KEGG	TGF-beta signaling pathway
PubGene	ID1
TreeFam	ID1
CTD	3397 [Comparative ToxicoGenomics Database]
	Other databases
	Probes
Probe	ID1 Related clones (RZPD - Berlin)
	PubMed
PubMed	85 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 18 14:45:50 2008