ATF2		ATF2 is a stress inducible basic leucine zipper transcription factor from the CREB family.  ATF2 is phosphorylated at threonine residues 69 and 71 by JNK or p38 mitogen activated protein kinases.  Mutation of these residues leads to the loss of ATF2 transactivation in vitro.	GeneCard:ATF2	http://www.genecards.org/cgi-bin/carddisp.pl?gene=ATF2
ATF2		ATF2 is a bZip transcription factor from the CREB family.  ATF2 binds to both cAMP response elements (TGACGTCA) and TPA responsive element (TGAGTCA) and is known to heterodimerize with JUN members of the AP1 family of transcription factors. ATF2 is activated by phosphorylation of Thr71 by the stress activated p38 mitogen activated protein kinases.	GeneCard:ATF2	http://www.genecards.org/cgi-bin/carddisp.pl?gene=ATF2
ATF2		This gene encodes a transcription factor that is a member of the leucine zipper family of DNA binding proteins. This protein binds to the cAMP-responsive element (CRE), an octameric palindrome. The protein forms a homodimer or heterodimer with c-Jun and stimulates CRE-dependent transcription. The protein is also a histone acetyltransferase (HAT) that specifically acetylates histones H2B and H4 in vitro; thus it may represent a class of sequence-specific factors that activate transcription by direct effects on chromatin components. Additional transcript variants have been identified but their biological validity has not been determined. (provided by RefSeq)	GeneCard:ATF2	http://www.genecards.org/cgi-bin/carddisp.pl?gene=ATF2
BCL11A		This gene encodes a C2H2 type zinc-finger protein by its similarity to the mouse Bcl11a/Evi9 protein. Functions as a myeloid and B-cell proto-oncogene. May play important roles in leukemogenesis and hematopoiesis. An essential factor in lymphopoiesis,is required for B-cell formation in fetal liver. May function as a modulator of the transcriptional repression activity of ARP1 (By similarity)	GeneCard:BCL11A	http://www.genecards.org/cgi-bin/carddisp.pl?gene=BCL11A
BCL11A		This gene encodes a C2H2 type zinc-finger protein by its similarity to the mouse Bcl11a/Evi9 protein. The corresponding mouse gene is a common site of retroviral integration in myeloid leukemia, and may function as a leukemia disease gene, in part, through its interaction with BCL6. During hematopoietic cell differentiation, this gene is down-regulated. It is possibly involved in lymphoma pathogenesis since translocations associated with B-cell malignancies also deregulates its expression. Multiple transcript variants encoding several different isoforms have been found for this gene. (provided by RefSeq)	GeneCard:BCL11A	http://www.genecards.org/cgi-bin/carddisp.pl?gene=BCL11A
BHLHE40		This gene encodes a basic helix-loop-helix protein expressed in various tissues. Expression in the chondrocytes is responsive to the addition of Bt2cAMP. The encoded protein is believed to be involved in the control of cell differe	GeneCard:BHLHE40	http://www.genecards.org/cgi-bin/carddisp.pl?gene=BHLHE40
BHLHE40		This gene encodes a basic helix-loop-helix protein expressed in various tissues. Expression in the chondrocytes is responsive to the addition of Bt2cAMP. The encoded protein is believed to be involved in the control of cell differentiation.	GeneCard:BHLHE40	http://www.genecards.org/cgi-bin/carddisp.pl?gene=BHLHE40
CEBPB		epitope mapping at the C-terminus of C/EBP-beta of rat origin	GeneCard:CEBPB	http://www.genecards.org/cgi-bin/carddisp.pl?gene=CEBPB
CEBPB		The protein encoded by this intronless gene is a bZIP transcription factor which can bind as a homodimer to certain DNA regulatory regions.  It can also form heterodimers with the related proteins CEBP-alpha, CEBP-delta, and CEBP-gamma.  The encoded protein is important in the regulation of genes involved in immune and inflammatory responses and has been shown to bind to the IL-1 response element in the IL-6 gene, as well as to regulatory regions of several acute-phase and cytokine genes.  In addition, the encoded protein can bind the promoter and upstream element and stimulate the expression of the collagen type I gene (provided by RefSeq).	GeneCard:CEBPB	http://www.genecards.org/cgi-bin/carddisp.pl?gene=CEBPB
CHD1		CHD1 is a member of the CHD (chromodomain-helicase-DNA-binding) family of proteins that interacts with nucleosomes and plays a role in chromatin remodeling to modulate transcription. The members of the CHD family of proteins possess 3 common structural and functional domains: a chromodomain (chromatin organization modifier), an SNF2-like helicase/ATPase domain, and a C-terminal DNA-binding domain. CHD1 has been shown to interact with the transcriptional corepressor NCoR and histone deacetylase 1 indicating a role in transcriptional regulation. CHD1 has also been shown to interact with the Paf1 complex and Rtf1 implicating an additional role in transcriptional elongation. Alternate names for CHD1 include chromodomain-helicase-DNA-binding protein 1, ATP-dependent helicase CHD1, and DKFZp686E2337.	GeneCard:CHD1	http://www.genecards.org/cgi-bin/carddisp.pl?gene=CHD1
CHD1		ATP-dependent chromatin-remodeling factor which functions as substrate recognition component of the transcription regulatory histone acetylation (HAT) complex SAGA. Regulates polymerase II transcription. Also required for efficient transcription by RNA polymerase I, and more specifically the polymerase I transcription termination step. Also required to maintain a specific chromatin configuration across the genome. Is also associated with histone deacetylase (HDAC) activity (By similarity). Required for the bridging of SNF2, the FACT complex, the PAF complex as well as the U2 snRNP complex to H3K4me3. Required for maintaining open chromatin and pluripotency in embryonic stem cells	GeneCard:CHD1	http://www.genecards.org/cgi-bin/carddisp.pl?gene=CHD1
CREB1		CREB is a basic leucine zipper transcription factor. CREB is activated by phosphorylation of Ser133 in response to a range of stimuli by including a number of transcription factors PKA, CAMK and MAPKs. CREB is ubiquitously expressed, but has been specifically implicated in the development in neurite outgrowth and neuronal differentiation.	GeneCard:CREB1	http://www.genecards.org/cgi-bin/carddisp.pl?gene=CREB1
CREB1		This gene encodes a transcription factor that is a member of the leucine zipper family of DNA binding proteins. This protein binds as a homodimer to the cAMP-responsive element, an octameric palindrome. The protein is phosphorylated by several protein kinases, and induces transcription of genes in response to hormonal stimulation of the cAMP pathway.  Alternate splicing of this gene results in two transcript variants encoding different isoforms. (provided by RefSeq)	GeneCard:CREB1	http://www.genecards.org/cgi-bin/carddisp.pl?gene=CREB1
CTCF		CTCF zinc finger transcription factor. A sequence specific DNA binding protein that functions as an insulator, blocking enhancer activity. It has also been suggested to block the spreading of chromatin structure in certain instances.	GeneCard:CTCF	http://www.genecards.org/cgi-bin/carddisp.pl?gene=CTCF
CTCF		Transcriptional regulator with 11 highly conserved zinc finger domains. Depending on context, can bind a histone acetyltransferase (HAT)-containing complex and function as transcriptional activator or bind a histone deacetylase (HDAC)-containing complex and function as transcriptional repressor. Involved in transcriptional regulation by binding to chromatin insulators and preventing interaction between promoter and nearby enhancers and silencers. Preferentially interacts with unmethylated DNA, preventing spreading of CpG methylation. Can dimerize, mediating long-range chromatin looping. When bound to chromatin, provides an anchor point for nucleosomes positioning. Involved in sister chromatid cohesion. Associates with both centromeres and chromosomal arms during metaphase and required for cohesin localization to CTCF sites.	GeneCard:CTCF	http://www.genecards.org/cgi-bin/carddisp.pl?gene=CTCF
CTCF		This gene is a member of the BORIS + CTCF gene family and encodes a transcriptional regulator protein with 11 highly conserved zinc finger (ZF) domains. This nuclear protein is able to use different combinations of the ZF domains to bind different DNA target sequences and proteins. (provided by RefSeq)	GeneCard:CTCF	http://www.genecards.org/cgi-bin/carddisp.pl?gene=CTCF
FOSL1		The Fos gene family consists of 4 members: FOS, FOSB, FOSL1, and FOSL2.  These genes encode leucine zipper proteins that can dimerize with proteins of the JUN family, thereby forming the transcription factor complex AP-1.  As such, the FOS proteins have been implicated as regulators of cell proliferation, differentiation, and transformation. (provided by RefSeq)	GeneCard:FOSL1	http://www.genecards.org/cgi-bin/carddisp.pl?gene=FOSL1
FOSL1		The Fos gene family consists of 4 members: FOS, FOSB, FOSL1, and FOSL2. These genes encode leucine zipper proteins that can dimerize with proteins of the JUN family, thereby forming the transcription factor complex AP-1. As such, the FOS proteins have been implicated as regulators of cell proliferation, differentiation, and transformation. (provided by RefSeq)	Genecard:FOSL1	http://www.genecards.org/cgi-bin/carddisp.pl?gene=FOSL1
FOXA1		This gene encodes a member of the forehead class of DNA-binding proteins. These hepatocyte nuclear factors are transcriptional activators for liver-specific transcripts such as albumin and transthyretin, and they also interact with chromatin. Similar family members in mice have roles in the regulation of metabolism and in the differentiation of the pancreas and liver (RefSeq).	GeneCard:FOXA1	http://www.genecards.org/cgi-bin/carddisp.pl?gene=FOXA1
FOXA1		This gene encodes a member of the forkhead class of DNA-binding proteins.  These hepatocyte nuclear factors are transcriptional activators for liver-specific transcripts such as albumin and transthyretin, and they also interact with chromatin. Similar family members in mice have roles in the regulation of metabolism and in the differentiation of the pancreas and liver. (provided by RefSeq)	GeneCard:FOXA1	http://www.genecards.org/cgi-bin/carddisp.pl?gene=FOXA1
GATA1		GATA-1 is a transcriptional activator which probably serves as a general switch factor for erythroid development. It binds to DNA sites with the consensus sequence [AT]GATA[AG} within regulatory regions of globin genes and of other genes expressed in erythroid cells.	GeneCard:GATA1	http://www.genecards.org/cgi-bin/carddisp.pl?gene=GATA1
GATA1		GATA1 is erythroid-specific and is responsible for the regulated transcription of erythroid genes.	GeneCard:Gata1	http://www.genecards.org/cgi-bin/carddisp.pl?gene=Gata1
GATA1		GATA1 is erythroid-specific and is responsible for the regulated transcription of erythroid genes.	GeneCard:Gata1	http://www.genecards.org/cgi-bin/carddisp.pl?gene=GATA1
GATA2		GATA2	GeneCard:GATA2	http://www.genecards.org/cgi-bin/carddisp.pl?gene=GATA2
GATA2		GATA binding protein 2	GeneCard:GATA2	http://www.genecards.org/cgi-bin/carddisp.pl?gene=GATA2
GATA2		This gene encodes a member of the GATA family of zinc-finger transcription factors that are named for the consensus nucleotide sequence they bind in the promoter regions of target genes. The encoded program plays an essential role in regulation transcription of genes involved in the development and proliferation of hematopoietic and endocrine cell lineages (RefSeq).	GeneCard:GATA2	http://www.genecards.org/cgi-bin/carddisp.pl?gene=GATA2
GATA2		The GATA family of transcription factors share a conserved zinc finger DNA-binding domain and are capable of binding the WGATAR consensus sequence. GATA1 is erythroid-specific and is essential for normal erythropeisis. By comparison, GATA2 is expressed at high levels in hematopoeitic progenitors, including early erythroid cells, but is strong repressed during erythroblast differentiaion.	GeneCard: GATA2	http://www.genecards.org/cgi-bin/carddisp.pl?gene=GATA2
GATA3		This gene encodes a protein which belongs to the GATA family of transcription factors.  The protein contains two GATA-type zinc fingers and is a n important regulator of T-cell development and plays an important role in endothelial cell biology.  Defects in this gene are the cause of hypoparathyroidism with sensorineural deafness and renal dysplasia (provided by RefSeq).	GeneCard:GATA3	http://www.genecards.org/cgi-bin/carddisp.pl?gene=GATA3
GATA3		This gene encodes a protein which belongs to the GATA family of transcription factors. The protein contains two GATA-type zinc fingers and is a n important regulator of T-cell development and plays an important role in endothelial cell biology. Defects in this gene are the cause of hypoparathyroidism with sensorineural deafness and renal dysplasia (provided by RefSeq)	Genecard:GATA3	http://www.genecards.org/cgi-bin/carddisp.pl?gene=GATA3