NFIB (nuclear factor I/B)

Identity

Other names	HMGIC/NFIB
	NFI-RED
	NFIB2
	NFIB3
HGNC	NFIB
Location	9p24.1
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	NFIB   7785
Entrez_Gene	NFIB  4781  nuclear factor I/B
	Cards
GeneCards	NFIB
Ensembl	NFIB [Search_View]   ENSG00000147862 [Gene_View]
Genatlas	NFIB
GeneLynx	NFIB
eGenome	NFIB
euGene	4781
	Genomic and cartography
GoldenPath	NFIB  -  9p24.1   chr9:14071847-14303945 -  9p23   [Description]    (hg18-March_2006)
Ensembl	NFIB - 9p23 [CytoView]
NCBI	Mapview
OMIM	Disease map [OMIM]
HomoloGene	NFIB
	Gene and transcription
Genbank	AF022215 [ ENTREZ ]
Genbank	AK094066 [ ENTREZ ]
Genbank	AK129782 [ ENTREZ ]
Genbank	AK131233 [ ENTREZ ]
Genbank	AK290603 [ ENTREZ ]
RefSeq	NM_005596 [ SRS ]    NM_005596 [ ENTREZ ]
RefSeq	AC_000052 [ SRS ]    AC_000052 [ ENTREZ ]
RefSeq	AC_000141 [ SRS ]    AC_000141 [ ENTREZ ]
RefSeq	NC_000009 [ SRS ]    NC_000009 [ ENTREZ ]
RefSeq	NT_008413 [ SRS ]    NT_008413 [ ENTREZ ]
RefSeq	NW_001839149 [ SRS ]    NW_001839149 [ ENTREZ ]
RefSeq	NW_924062 [ SRS ]    NW_924062 [ ENTREZ ]
AceView	NFIB AceView - NCBI
Unigene	Hs.709255 [ SRS ]    Hs.709255 [ NCBI ]     HS709255 [ spliceNest ]
Fast-db	2496 (alternative variants)
	Protein : pattern, domain, 3D structure
SwissProt	O00712 [ SRS]    O00712 [ EXPASY ]     O00712 [ INTERPRO ]     O00712 [ UNIPROT ]
Prosite	PS00349 CTF_NFI_1 [ SRS ]    PS00349 CTF_NFI_1 [ Expasy ]
Prosite	PS51080 CTF_NFI_2 [ SRS ]    PS51080 CTF_NFI_2 [ Expasy ]
Interpro	IPR000647 CTF_NFI [ SRS ]    IPR000647 CTF_NFI [ EBI ]
Interpro	IPR003619 MH1_Dwarfin-type [ SRS ]    IPR003619 MH1_Dwarfin-type [ EBI ]
CluSTr	O00712
Pfam	PF00859 CTF_NFI [ SRS ]    PF00859 CTF_NFI [ Sanger ]    pfam00859 [ NCBI-CDD ]
Pfam	PF03165 MH1 [ SRS ]    PF03165 MH1 [ Sanger ]    pfam03165 [ NCBI-CDD ]
Smart	SM00523 DWA [EMBL]
Blocks	O00712
HPRD	09008
	Protein Interaction databases
DIP	O00712
IntAct	O00712
	Polymorphism : SNP, mutations, diseases
OMIM	600728    [ map ]
GENECLINICS	600728
SNP	NFIB [dbSNP-NCBI]
SNP	NM_005596 [SNP-NCI]
SNP	NFIB [GeneSNPs - Utah]  NFIB] [HGBASE - SRS]
HAPMAP	NFIB [HAPMAP]
COSMIC	NFIB [Somatic mutation (COSMIC-CGP-Sanger)]
HGMD	NFIB
	General knowledge
Family Browser	NFIB [UCSC Family Browser]
SOURCE	NM_005596
SMD	Hs.709255
SAGE	Hs.709255
GO	transcription factor activity [Amigo]  transcription factor activity
GO	transcription factor activity [Amigo]  transcription factor activity
GO	intracellular [Amigo]  intracellular
GO	nucleus [Amigo]  nucleus
GO	nucleus [Amigo]  nucleus
GO	DNA replication [Amigo]  DNA replication
GO	transcription [Amigo]  transcription
GO	regulation of transcription, DNA-dependent [Amigo]  regulation of transcription, DNA-dependent
PubGene	NFIB
TreeFam	NFIB
CTD	4781 [Comparative ToxicoGenomics Database]
	Other databases
	Probes
Probe	NFIB Related clones (RZPD - Berlin)
	PubMed
PubMed	11 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
Updated	03-2008	Dessen P

© Atlas of Genetics and Cytogenetics in Oncology and Haematology

indexed on : Mon Aug 11 20:22:01 2008