| Type |
Details |
Score |
| Publication |
| First Author: |
Nissen RM |
| Year: |
2006 |
| Journal: |
BMC Dev Biol |
| Title: |
A zebrafish screen for craniofacial mutants identifies wdr68 as a highly conserved gene required for endothelin-1 expression. |
| Volume: |
6 |
|
| Pages: |
28 |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Park J |
| Year: |
2013 |
| Journal: |
Exp Neurobiol |
| Title: |
New Perspectives of Dyrk1A Role in Neurogenesis and Neuropathologic Features of Down Syndrome. |
| Volume: |
22 |
| Issue: |
4 |
| Pages: |
244-8 |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Leslie EJ |
| Year: |
2016 |
| Journal: |
Hum Mol Genet |
| Title: |
A multi-ethnic genome-wide association study identifies novel loci for non-syndromic cleft lip with or without cleft palate on 2p24.2, 17q23 and 19q13. |
| Volume: |
25 |
| Issue: |
13 |
| Pages: |
2862-2872 |
|
•
•
•
•
•
|
| Protein Domain |
| Type: |
Conserved_site |
| Description: |
The cryptochrome and photolyase families consist of structurally related flavin adenine dinucleotide (FAD) proteins that use the absorption of blue light to accomplish different tasks. The photolyasess use the blue light for light-driven electron transfer to repair UV-damaged DNA, while the cryptochromes are blue-light photoreceptors involved in the circadian clock for plants and animals [, ]. On the basis of the primary structure, the cryptochrome/DNA photolyase family can be grouped into two classes []. The first class contains cryptochromes and DNA photolyases from eubacteria, archaea, fungi, animals and plants. The second class contains DNA photolyases from prokaryotes, plants and animals.This entry represents a number of conserved sequence regions found in the C-terminal region of the class 1 cryptochrome/DNA photolyase. |
|
•
•
•
•
•
|
| Protein Domain |
| Type: |
Family |
| Description: |
The cryptochrome and photolyase families consist of structurally related flavin adenine dinucleotide (FAD) proteins that use the absorption of blue light to accomplish different tasks. The photolyasess use the blue light for light-driven electron transfer to repair UV-damaged DNA, while the cryptochromes are blue-light photoreceptors involved in the circadian clock for plants and animals [, ]. On the basis of the primary structure, the cryptochrome/DNA photolyase family can be grouped into two classes []. The first class contains cryptochromes and DNA photolyases from eubacteria, archaea, fungi, animals and plants. The second class contains DNA photolyases from prokaryotes, plants and animals.This entry represents the class1 cryptochrome/DNA photolyase family. Its members include cryptochromes, DNA photolyases and cryptochrome-DASH (Cry-DASH). The Cry-DASH family members have been shown to act as photolyases with high degree of specificity for cyclobutane pyrimidine dimers in ssDNA []. |
|
•
•
•
•
•
|
| Protein Domain |
| Type: |
Family |
| Description: |
In Drosophila melanogaster (Fruit fly) the preprocorazonin consists of an 19 amino acid signal peptide, the 11 amino acid corazonin sequence followed by a 39 amino acid corazonin-precursor-related peptide (CPRP) and finally the 85 amino acid propeptide, [].Corazonin is a cardioactive peptide of insects, which is probably involved in the physiological regulation of the heart beat. Drosophila clock (clk) and cycle (cyc) proteins negatively regulate Crz transcription in a cell-specific manner []. Corazonin is expressed in neurosecretory neurons of the pars lateralis of the protocerebrum and transported via nervi corporis cardiaci to the storage lobes of the corpora cardiaca. The peptide occurs with a single isoform in all insects studied so far, with the exception of the Coleoptera in which none could be detected []. |
|
•
•
•
•
•
|
| Protein Domain |
| Type: |
Domain |
| Description: |
This entry represents the C-terminal catalytic domain of the deadenylase nocturnin, and related domains. Nocturnin is a poly(A)-specific 3' exonuclease that specifically degrades the 3' poly(A) tail of RNA in a process known as deadenylation. This nuclease activity is manganese dependent. Nocturnin is expressed in the cytoplasm of Xenopus laevis retinal photoreceptor cells in a rhythmic fashion, and it has been proposed that it participates in posttranscriptional regulation of the circadian clock or its outputs, and that the mRNA target(s) of this deadenylase are circadian clock-related []. In mouse, the nocturnin gene, mNoc, is expressed in a circadian pattern in a range of tissues including retina, spleen, heart, kidney, and liver. It is highly expressed in bone-marrow stromal cells, adipocytes and hepatocytes []. In mammals, nocturnin plays a role in regulating mesenchymal stem-cell lineage allocation, perhaps through regulating PPAR-gamma (peroxisome proliferator-activated receptor-gamma) nuclear translocation []. |
|
•
•
•
•
•
|
| Protein Domain |
| Type: |
Conserved_site |
| Description: |
The cryptochrome and photolyase families consist of structurally related flavin adenine dinucleotide (FAD) proteins that use the absorption of blue light to accomplish different tasks. The photolyasess use the blue light for light-driven electron transfer to repair UV-damaged DNA, while the cryptochromes are blue-light photoreceptors involved in the circadian clock for plants and animals [, ]. On the basis of the primary structure, the cryptochrome/DNA photolyase family can be grouped into two classes []. The first class contains cryptochromes and DNA photolyases from eubacteria, archaea, fungi, animals and plants. The second class contains DNA photolyases from prokaryotes, plants and animals.This entry represents a number of conserved sequence regions found in the C-terminal region of the class 2 DNA photolyases. |
|
•
•
•
•
•
|
| Protein Domain |
| Type: |
Domain |
| Description: |
Proteins in this entry belong to a family of dinoflagellate luciferase and luciferin binding proteins. Luciferase is involved in catalysing the light emitting reaction in bioluminescence and luciferin binding protein (LBP) is known to bind to luciferin (the substrate for luciferase) to stop it reacting with the enzyme and therefore switching off the bioluminescence function. The expression of these two proteins is controlled by a circadian clock at the translational level, with synthesis and degradation occurring on a daily basis [].This entry consists of a presumed N-terminal domain that is conserved between dinoflagellateluciferase and luciferin binding proteins. This domain is not, however, the catalytic part of the protein. It has been suggested that this region may mediate an interaction between LBP and Luciferase or their association with the vacuolar membrane []. |
|
•
•
•
•
•
|
| Protein Domain |
| Type: |
Domain |
| Description: |
The prokineticin family includes prokinectin itself and related proteins such as BM8 and the AVIToxins. The suprachiasmatic nucleus (SCN) controls the circadian rhythm of physiological and behavioural processes in mammals. It has been shown that prokineticin 2 (PK2), a cysteine-rich secreted protein, functions as an output molecule from the SCN circadian clock. PK2 messenger RNA is rhythmically expressed in the SCN, and the phase of PK2 rhythm is responsive to light entrainment. Molecular and genetic studies have revealed that PK2 is a gene that is controlled by a circadian clock [].The prokinectin domain is found in the prokinectin family and the hainantoxins, where it comprises the whole length of the protein. This domain is also found at the C terminus of some members of the Dickkopf family. |
|
•
•
•
•
•
|
| Protein Domain |
| Type: |
Family |
| Description: |
The cryptochrome and photolyase families consist of structurally related flavin adenine dinucleotide (FAD) proteins that use the absorption of blue light to accomplish different tasks. The photolyasess use the blue light for light-driven electron transfer to repair UV-damaged DNA, while the cryptochromes are blue-light photoreceptors involved in the circadian clock for plants and animals [, ]. On the basis of the primary structure, the cryptochrome/DNA photolyase family can be grouped into two classes []. The first class contains cryptochromes and DNA photolyases from eubacteria, archaea, fungi, animals and plants. The second class contains DNA photolyases from prokaryotes, plants and animals.Similar to the distantly related microbial class I photolyases, class 2 enzymes repair UV-induced cyclobutane pyrimidine dimer (CPD) lesions within duplex DNA using blue/near-UV light []. There are a number of conserved sequence regions in all known class 2 DNA photolyases, especially in the C-terminal part. The structures of the class 2 DNA photolyase from archaea and rice have been solved [, ]. |
|
•
•
•
•
•
|
| Protein Domain |
| Type: |
Family |
| Description: |
This entry represents a group of WD repeat-containing proteins, including DCAF7 from animals, LWD1/2/TTG1 from Arabidopsis and YPL247C from budding yeasts. In general, WD40 repeat domain-containing proteins are scaffolding elements for the assembly of multi-subunit protein complexes. DCAF7, also known as WDR68, interacts with Dual-specificity Tyrosine Phosphorylation-Regulated Kinase 1A (DYRK1A, a Down's syndrome-associated protein kinase) []and is required for Endothelin-1 (EDN1) signalling []. It also acts as a DDB1- and CUL4-associated factor []. Mutations in the DCAF7 gene have been linked to cleft lip with or without cleft palate (CL/P) []. In Arabidopsis, LWD1 and LWD2 serve as clock proteins involved in photoperiod flowering control []. TRANSPARENT TESTA GLABRA 1 (TTG1) is a regulator of early developmental traits and is also involved in flowering time regulation []. |
|
•
•
•
•
•
|
| Protein Domain |
| Type: |
Family |
| Description: |
This entry represents the DNA damage-binding protein 1 (DDB1) family, whose members are involved in DNA repair.The fission yeast members in this family includes Rik1 and Ddb1. Rik1 is a component of the Rik1-associated E3 ubiquitin ligase complex that shows ubiquitin ligase activity and is required for histone H3K9 methylation []. Ddb1 is a component of cullin 4A ubiquitin ligases, which regulates the selective proteolysis of key proteins in DNA repair, replication and transcription [, ].Mammalian Ddb1 is apart of the CUL4-DDB1 ubiquitin E3 ligase that regulates cell-cycle progression, replication and DNA damage response. The CUL4-DDB1 ubiquitin E3 ligase interacts with multiple WD40-repeat proteins and regulates histone methylation []. This complex also regulates the circadian clock function by mediating the ubiquitination and degradation of CRY1 [].The plant Ddb1 is part of the CUL4-DDB1-DDB2 E3 ligase involved in maintaining genome integrity upon UV stress []. |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Harada Y |
| Year: |
2005 |
| Journal: |
J Biol Chem |
| Title: |
Ser-557-phosphorylated mCRY2 is degraded upon synergistic phosphorylation by glycogen synthase kinase-3 beta. |
| Volume: |
280 |
| Issue: |
36 |
| Pages: |
31714-21 |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Masana MI |
| Year: |
2007 |
| Journal: |
Am J Physiol Regul Integr Comp Physiol |
| Title: |
Behavioral characterization and modulation of circadian rhythms by light and melatonin in C3H/HeN mice homozygous for the RORbeta knockout. |
| Volume: |
292 |
| Issue: |
6 |
| Pages: |
R2357-67 |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Alvarez-López C |
| Year: |
2004 |
| Journal: |
Brain Res |
| Title: |
Altered endogenous activation of CREB in the suprachiasmatic nucleus of mice with retinal degeneration. |
| Volume: |
1024 |
| Issue: |
1-2 |
| Pages: |
137-45 |
|
•
•
•
•
•
|
| HT Experiment |
| Series Id: |
GSE59460 |
| Experiment Type: |
transcription profiling by array |
| Study Type: |
WT vs. Mutant |
| Source: |
ArrayExpress |
|
•
•
•
•
•
|
| HT Experiment |
|
| Experiment Type: |
RNA-Seq |
| Study Type: |
Baseline |
| Source: |
GEO |
|
•
•
•
•
•
|
| HT Experiment |
|
| Experiment Type: |
transcription profiling by array |
| Study Type: |
Baseline |
| Source: |
GEO |
|
•
•
•
•
•
|
| HT Experiment |
|
| Experiment Type: |
transcription profiling by array |
| Study Type: |
Baseline |
| Source: |
GEO |
|
•
•
•
•
•
|
| HT Experiment |
|
| Experiment Type: |
transcription profiling by array |
| Study Type: |
Baseline |
| Source: |
ArrayExpress |
|
•
•
•
•
•
|
| HT Experiment |
|
| Experiment Type: |
RNA-Seq |
| Study Type: |
WT vs. Mutant |
| Source: |
GEO |
|
•
•
•
•
•
|
| HT Experiment |
|
| Experiment Type: |
RNA-Seq |
| Study Type: |
WT vs. Mutant |
| Source: |
GEO |
|
•
•
•
•
•
|
| HT Experiment |
|
| Experiment Type: |
RNA-Seq |
| Study Type: |
WT vs. Mutant |
| Source: |
GEO |
|
•
•
•
•
•
|
| HT Experiment |
|
| Experiment Type: |
RNA-Seq |
| Study Type: |
Baseline |
| Source: |
GEO |
|
•
•
•
•
•
|
| HT Experiment |
| Series Id: |
GSE70440 |
| Experiment Type: |
RNA-Seq |
| Study Type: |
WT vs. Mutant |
| Source: |
ArrayExpress |
|
•
•
•
•
•
|
| HT Experiment |
|
| Experiment Type: |
RNA-Seq |
| Study Type: |
Baseline |
| Source: |
GEO |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Delumeau O |
| Year: |
2004 |
| Journal: |
J Biol Chem |
| Title: |
Functional and structural characterization of RsbU, a stress signaling protein phosphatase 2C. |
| Volume: |
279 |
| Issue: |
39 |
| Pages: |
40927-37 |
|
•
•
•
•
•
|
| Protein Domain |
| Type: |
Domain |
| Description: |
This entry represents the N-terminal domain of the Timeless protein. The timeless gene in Drosophila melanogasteris involved in circadian rhythm control []. Drosophila contains two paralogs, dTIM and dTIM2, acting in clock/photoreception and chromosome integrity/photoreception respectively. The mammalian TIMELESS (TIM) protein, originally identified based on its similarity to Drosophila dTIM, interacts with the clock proteins dCRY and dPER and is essential for circadian rhythm generation and photo-entrainment in the fly []. However, phylogenetic sequence analysis has demonstrated that dTIM2 is likely to be the orthologue of mammalian TIM and other widely conserved TIM-like proteins in eukaryotes []. These proteins include Saccharomyces cerevisiae Tof1, Schizosaccharomyces pombe Swi1, and Caenorhabditis elegans TIM. These proteins are not involved in the core clock mechanism, but instead play important roles in chromosome integrity, efficient cell growth and/or development [, ], with the exception of dTIM-2, that has an additional function in retinal photoreception [].Saccharomyces cerevisiae Tof1 is a subunit of a replication-pausing checkpoint complex (Tof1-Mrc1-Csm3) that acts at the stalled replication fork to promote sister chromatid cohesion after DNA damage, facilitating gap repair of damaged DNA [, ]. Schizosaccharomyces pombe Swi1 and Swi3 form the fork protection complex that coordinates leading- and lagging-strand synthesis and stabilizes stalled replication forks []. In humans timeless forms a stable complex with its partner protein Tipin. The Timeless-Tipin complex has been reported to travel along with the replication fork during unperturbed DNA replication. Moreover, the Timeless-Tipin-Claspin complex contributes to full activation of the ATR-Chk1 signaling pathway through the recruitment of Chk1 to arrested replication forks for sufficient ATR-mediated phosphorylation. It also interacts with PARP-1, and this interaction is required for efficient homologous recombination repair []. |
|
•
•
•
•
•
|
| Protein Domain |
| Type: |
Domain |
| Description: |
This entry represents the C-terminal domain found in the Timeless (TIM) proteins. This domain can be found in TIM homologues mostly from animals. This domain found in hTIM has been shown to bind to the PARP-1 catalytic domain [].The timeless gene in Drosophila melanogasteris involved in circadian rhythm control []. Drosophila contains two paralogs, dTIM and dTIM2, acting in clock/photoreception and chromosome integrity/photoreception respectively. The mammalian TIMELESS (TIM) protein, originally identified based on its similarity to Drosophila dTIM, interacts with the clock proteins dCRY and dPER and is essential for circadian rhythm generation and photo-entrainment in the fly []. However, phylogenetic sequence analysis has demonstrated that dTIM2 is likely to be the orthologue of mammalian TIM and other widely conserved TIM-like proteins in eukaryotes []. These proteins include Saccharomyces cerevisiae Tof1, Schizosaccharomyces pombe Swi1, and Caenorhabditis elegans TIM. These proteins are not involved in the core clock mechanism, but instead play important roles in chromosome integrity, efficient cell growth and/or development [, ], with the exception of dTIM-2, that has an additional function in retinal photoreception [].Saccharomyces cerevisiae Tof1 is a subunit of a replication-pausing checkpoint complex (Tof1-Mrc1-Csm3) that acts at the stalled replication fork to promote sister chromatid cohesion after DNA damage, facilitating gap repair of damaged DNA [, ]. Schizosaccharomyces pombe Swi1 and Swi3 form the fork protection complex that coordinates leading- and lagging-strand synthesis and stabilizes stalled replication forks []. In humans timeless forms a stable complex with its partner protein Tipin. The Timeless-Tipin complex has been reported to travel along with the replication fork during unperturbed DNA replication. Moreover, the Timeless-Tipin-Claspin complex contributes to full activation of the ATR-Chk1 signaling pathway through the recruitment of Chk1 to arrested replication forks for sufficient ATR-mediated phosphorylation. It also interacts with PARP-1, and this interaction is required for efficient homologous recombination repair []. |
|
•
•
•
•
•
|
| Protein Domain |
| Type: |
Family |
| Description: |
The timeless gene in Drosophila melanogasteris involved in circadian rhythm control []. Drosophila contains two paralogs, dTIM and dTIM2, acting in clock/photoreception and chromosome integrity/photoreception respectively. The mammalian TIMELESS (TIM) protein, originally identified based on its similarity to Drosophila dTIM, interacts with the clock proteins dCRY and dPER and is essential for circadian rhythm generation and photo-entrainment in the fly []. However, phylogenetic sequence analysis has demonstrated that dTIM2 is likely to be the orthologue of mammalian TIM and other widely conserved TIM-like proteins in eukaryotes []. These proteins include Saccharomyces cerevisiae Tof1, Schizosaccharomyces pombe Swi1, and Caenorhabditis elegans TIM. These proteins are not involved in the core clock mechanism, but instead play important roles in chromosome integrity, efficient cell growth and/or development [, ], with the exception of dTIM-2, that has an additional function in retinal photoreception [].Saccharomyces cerevisiae Tof1 is a subunit of a replication-pausing checkpoint complex (Tof1-Mrc1-Csm3) that acts at the stalled replication fork to promote sister chromatid cohesion after DNA damage, facilitating gap repair of damaged DNA [, ]. Schizosaccharomyces pombe Swi1 and Swi3 form the fork protection complex that coordinates leading- and lagging-strand synthesis and stabilizes stalled replication forks []. In humans timeless forms a stable complex with its partner protein Tipin. The Timeless-Tipin complex has been reported to travel along with the replication fork during unperturbed DNA replication. Moreover, the Timeless-Tipin-Claspin complex contributes to full activation of the ATR-Chk1 signaling pathway through the recruitment of Chk1 to arrested replication forks for sufficient ATR-mediated phosphorylation. It also interacts with PARP-1, and this interaction is required for efficient homologous recombination repair []. |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Sakhi K |
| Year: |
2014 |
| Journal: |
J Physiol |
| Title: |
Daily variation in the electrophysiological activity of mouse medial habenula neurones. |
| Volume: |
592 |
| Issue: |
4 |
| Pages: |
587-603 |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Ono D |
| Year: |
2013 |
| Journal: |
PLoS One |
| Title: |
Postnatal constant light compensates Cryptochrome1 and 2 double deficiency for disruption of circadian behavioral rhythms in mice under constant dark. |
| Volume: |
8 |
| Issue: |
11 |
| Pages: |
e80615 |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Gaitonde KD |
| Year: |
2023 |
| Journal: |
PLoS One |
| Title: |
Diurnal regulation of metabolism by Gs-alpha in hypothalamic QPLOT neurons. |
| Volume: |
18 |
| Issue: |
5 |
| Pages: |
e0284824 |
|
•
•
•
•
•
|
| Protein |
| Organism: |
Mus musculus/domesticus |
| Length: |
1197
 |
| Fragment?: |
false |
|
•
•
•
•
•
|
| Protein |
| Organism: |
Mus musculus/domesticus |
| Length: |
1196
 |
| Fragment?: |
false |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Rosato E |
| Year: |
2001 |
| Journal: |
Philos Trans R Soc Lond B Biol Sci |
| Title: |
Flies, clocks and evolution. |
| Volume: |
356 |
| Issue: |
1415 |
| Pages: |
1769-78 |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Noguchi E |
| Year: |
2004 |
| Journal: |
Mol Cell Biol |
| Title: |
Swi1 and Swi3 are components of a replication fork protection complex in fission yeast. |
| Volume: |
24 |
| Issue: |
19 |
| Pages: |
8342-55 |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Katou Y |
| Year: |
2003 |
| Journal: |
Nature |
| Title: |
S-phase checkpoint proteins Tof1 and Mrc1 form a stable replication-pausing complex. |
| Volume: |
424 |
| Issue: |
6952 |
| Pages: |
1078-83 |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Xie S |
| Year: |
2015 |
| Journal: |
Mol Cell |
| Title: |
Timeless Interacts with PARP-1 to Promote Homologous Recombination Repair. |
| Volume: |
60 |
| Issue: |
1 |
| Pages: |
163-76 |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Bando M |
| Year: |
2009 |
| Journal: |
J Biol Chem |
| Title: |
Csm3, Tof1, and Mrc1 form a heterotrimeric mediator complex that associates with DNA replication forks. |
| Volume: |
284 |
| Issue: |
49 |
| Pages: |
34355-65 |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Ceriani MF |
| Year: |
1999 |
| Journal: |
Science |
| Title: |
Light-dependent sequestration of TIMELESS by CRYPTOCHROME. |
| Volume: |
285 |
| Issue: |
5427 |
| Pages: |
553-6 |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Benna C |
| Year: |
2000 |
| Journal: |
Curr Biol |
| Title: |
A second timeless gene in Drosophila shares greater sequence similarity with mammalian tim. |
| Volume: |
10 |
| Issue: |
14 |
| Pages: |
R512-3 |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Grabarczyk DB |
| Year: |
2020 |
| Journal: |
Nucleic Acids Res |
| Title: |
Crystal structure and interactions of the Tof1-Csm3 (Timeless-Tipin) fork protection complex. |
| Volume: |
48 |
| Issue: |
12 |
| Pages: |
6996-7004 |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Chaix A |
| Year: |
2019 |
| Journal: |
Cell Metab |
| Title: |
Time-Restricted Feeding Prevents Obesity and Metabolic Syndrome in Mice Lacking a Circadian Clock. |
| Volume: |
29 |
| Issue: |
2 |
| Pages: |
303-319.e4 |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Okada A |
| Year: |
2005 |
| Journal: |
Birth Defects Res A Clin Mol Teratol |
| Title: |
Identification of early-responsive genes correlated to valproic acid-induced neural tube defects in mice. |
| Volume: |
73 |
| Issue: |
4 |
| Pages: |
229-38 |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Kriebs A |
| Year: |
2017 |
| Journal: |
Proc Natl Acad Sci U S A |
| Title: |
Circadian repressors CRY1 and CRY2 broadly interact with nuclear receptors and modulate transcriptional activity. |
| Volume: |
114 |
| Issue: |
33 |
| Pages: |
8776-8781 |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Zhang EE |
| Year: |
2010 |
| Journal: |
Nat Med |
| Title: |
Cryptochrome mediates circadian regulation of cAMP signaling and hepatic gluconeogenesis. |
| Volume: |
16 |
| Issue: |
10 |
| Pages: |
1152-6 |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Gao P |
| Year: |
2013 |
| Journal: |
J Biol Chem |
| Title: |
Phosphorylation of the cryptochrome 1 C-terminal tail regulates circadian period length. |
| Volume: |
288 |
| Issue: |
49 |
| Pages: |
35277-86 |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Valekunja UK |
| Year: |
2013 |
| Journal: |
Proc Natl Acad Sci U S A |
| Title: |
Histone methyltransferase MLL3 contributes to genome-scale circadian transcription. |
| Volume: |
110 |
| Issue: |
4 |
| Pages: |
1554-9 |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Kang TH |
| Year: |
2011 |
| Journal: |
Nucleic Acids Res |
| Title: |
Regulation of nucleotide excision repair activity by transcriptional and post-transcriptional control of the XPA protein. |
| Volume: |
39 |
| Issue: |
8 |
| Pages: |
3176-87 |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Masuki S |
| Year: |
2005 |
| Journal: |
J Physiol |
| Title: |
Reduced alpha-adrenoceptor responsiveness and enhanced baroreflex sensitivity in Cry-deficient mice lacking a biological clock. |
| Volume: |
566 |
| Issue: |
Pt 1 |
| Pages: |
213-24 |
|
•
•
•
•
•
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| Publication |
| First Author: |
Czarna A |
| Year: |
2011 |
| Journal: |
J Biol Chem |
| Title: |
Quantitative analyses of cryptochrome-mBMAL1 interactions: mechanistic insights into the transcriptional regulation of the mammalian circadian clock. |
| Volume: |
286 |
| Issue: |
25 |
| Pages: |
22414-25 |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Clark JF |
| Year: |
2024 |
| Journal: |
Genes Dev |
| Title: |
Diverse Fgfr1 signaling pathways and endocytic trafficking regulate mesoderm development. |
|
|
|
|
•
•
•
•
•
|
| Publication |
| First Author: |
Yasui A |
| Year: |
1994 |
| Journal: |
EMBO J |
| Title: |
A new class of DNA photolyases present in various organisms including aplacental mammals. |
| Volume: |
13 |
| Issue: |
24 |
| Pages: |
6143-51 |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Petkau N |
| Year: |
2019 |
| Journal: |
Elife |
| Title: |
Acetylation of BMAL1 by TIP60 controls BRD4-P-TEFb recruitment to circadian promoters. |
| Volume: |
8 |
|
|
|
•
•
•
•
•
|
| Publication |
| First Author: |
Dequéant ML |
| Year: |
2006 |
| Journal: |
Science |
| Title: |
A complex oscillating network of signaling genes underlies the mouse segmentation clock. |
| Volume: |
314 |
| Issue: |
5805 |
| Pages: |
1595-8 |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Vermot J |
| Year: |
2005 |
| Journal: |
Science |
| Title: |
Retinoic acid controls the bilateral symmetry of somite formation in the mouse embryo. |
| Volume: |
308 |
| Issue: |
5721 |
| Pages: |
563-6 |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Hayter EA |
| Year: |
2021 |
| Journal: |
Nat Commun |
| Title: |
Distinct circadian mechanisms govern cardiac rhythms and susceptibility to arrhythmia. |
| Volume: |
12 |
| Issue: |
1 |
| Pages: |
2472 |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Ruby NF |
| Year: |
2002 |
| Journal: |
Science |
| Title: |
Role of melanopsin in circadian responses to light. |
| Volume: |
298 |
| Issue: |
5601 |
| Pages: |
2211-3 |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Feng D |
| Year: |
2011 |
| Journal: |
Science |
| Title: |
A circadian rhythm orchestrated by histone deacetylase 3 controls hepatic lipid metabolism. |
| Volume: |
331 |
| Issue: |
6022 |
| Pages: |
1315-9 |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Harmar AJ |
| Year: |
2002 |
| Journal: |
Cell |
| Title: |
The VPAC(2) receptor is essential for circadian function in the mouse suprachiasmatic nuclei. |
| Volume: |
109 |
| Issue: |
4 |
| Pages: |
497-508 |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Hirata H |
| Year: |
2002 |
| Journal: |
Science |
| Title: |
Oscillatory expression of the bHLH factor Hes1 regulated by a negative feedback loop. |
| Volume: |
298 |
| Issue: |
5594 |
| Pages: |
840-3 |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Barone I |
| Year: |
2023 |
| Journal: |
Sci Adv |
| Title: |
Synaptic BMAL1 phosphorylation controls circadian hippocampal plasticity. |
| Volume: |
9 |
| Issue: |
43 |
| Pages: |
eadj1010 |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Tafti M |
| Year: |
1997 |
| Journal: |
Neuroreport |
| Title: |
Localization of candidate genomic regions influencing paradoxical sleep in mice. |
| Volume: |
8 |
| Issue: |
17 |
| Pages: |
3755-8 |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Green CB |
| Year: |
1998 |
| Journal: |
Trends Cell Biol |
| Title: |
How cells tell time. |
| Volume: |
8 |
| Issue: |
6 |
| Pages: |
224-30 |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Yin L |
| Year: |
2007 |
| Journal: |
Science |
| Title: |
Rev-erbalpha, a heme sensor that coordinates metabolic and circadian pathways. |
| Volume: |
318 |
| Issue: |
5857 |
| Pages: |
1786-9 |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Yu EA |
| Year: |
2011 |
| Journal: |
Aging (Albany NY) |
| Title: |
Disrupting the circadian clock: gene-specific effects on aging, cancer, and other phenotypes. |
| Volume: |
3 |
| Issue: |
5 |
| Pages: |
479-93 |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Shafi AA |
| Year: |
2019 |
| Journal: |
Cancer Res |
| Title: |
Cancer and the Circadian Clock. |
| Volume: |
79 |
| Issue: |
15 |
| Pages: |
3806-3814 |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Mia S |
| Year: |
2023 |
| Journal: |
JACC Basic Transl Sci |
| Title: |
Novel Roles for the Transcriptional Repressor E4BP4 in Both Cardiac Physiology and Pathophysiology. |
| Volume: |
8 |
| Issue: |
9 |
| Pages: |
1141-1156 |
|
•
•
•
•
•
|
| Protein Coding Gene |
| Type: |
protein_coding_gene |
| Organism: |
mouse, laboratory |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Kurabayashi N |
| Year: |
2010 |
| Journal: |
Mol Cell Biol |
| Title: |
DYRK1A and glycogen synthase kinase 3beta, a dual-kinase mechanism directing proteasomal degradation of CRY2 for circadian timekeeping. |
| Volume: |
30 |
| Issue: |
7 |
| Pages: |
1757-68 |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Marcheva B |
| Year: |
2022 |
| Journal: |
Elife |
| Title: |
P2Y1 purinergic receptor identified as a diabetes target in a small-molecule screen to reverse circadian β-cell failure. |
| Volume: |
11 |
|
|
|
•
•
•
•
•
|
| Publication |
| First Author: |
Liu Z |
| Year: |
2020 |
| Journal: |
Proc Natl Acad Sci U S A |
| Title: |
Circadian regulation of c-MYC in mice. |
| Volume: |
117 |
| Issue: |
35 |
| Pages: |
21609-21617 |
|
•
•
•
•
•
|
| HT Experiment |
| Series Id: |
GSE9471 |
| Experiment Type: |
transcription profiling by array |
| Study Type: |
Baseline |
| Source: |
ArrayExpress |
|
•
•
•
•
•
|
| HT Experiment |
| Series Id: |
GSE38624 |
| Experiment Type: |
transcription profiling by array |
| Study Type: |
WT vs. Mutant |
| Source: |
ArrayExpress |
|
•
•
•
•
•
|
| HT Experiment |
| Series Id: |
GSE38623 |
| Experiment Type: |
transcription profiling by array |
| Study Type: |
Baseline |
| Source: |
ArrayExpress |
|
•
•
•
•
•
|
| HT Experiment |
| Series Id: |
GSE38622 |
| Experiment Type: |
transcription profiling by array |
| Study Type: |
Baseline |
| Source: |
ArrayExpress |
|
•
•
•
•
•
|
| HT Experiment |
|
| Experiment Type: |
RNA-Seq |
| Study Type: |
Baseline |
| Source: |
GEO |
|
•
•
•
•
•
|
| HT Experiment |
|
| Experiment Type: |
RNA-Seq |
| Study Type: |
Baseline |
| Source: |
GEO |
|
•
•
•
•
•
|
| HT Experiment |
|
| Experiment Type: |
RNA-Seq |
| Study Type: |
Baseline |
| Source: |
GEO |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Takasu NN |
| Year: |
2012 |
| Journal: |
PLoS One |
| Title: |
Circadian regulation of food-anticipatory activity in molecular clock-deficient mice. |
| Volume: |
7 |
| Issue: |
11 |
| Pages: |
e48892 |
|
•
•
•
•
•
|
| Protein |
| Organism: |
Mus musculus/domesticus |
| Length: |
243
 |
| Fragment?: |
true |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Park HW |
| Year: |
1995 |
| Journal: |
Science |
| Title: |
Crystal structure of DNA photolyase from Escherichia coli. |
| Volume: |
268 |
| Issue: |
5219 |
| Pages: |
1866-72 |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Kort R |
| Year: |
2004 |
| Journal: |
Acta Crystallogr D Biol Crystallogr |
| Title: |
DNA apophotolyase from Anacystis nidulans: 1.8 A structure, 8-HDF reconstitution and X-ray-induced FAD reduction. |
| Volume: |
60 |
| Issue: |
Pt 7 |
| Pages: |
1205-13 |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Molusky MM |
| Year: |
2012 |
| Journal: |
PLoS One |
| Title: |
Peroxisomal localization and circadian regulation of ubiquitin-specific protease 2. |
| Volume: |
7 |
| Issue: |
11 |
| Pages: |
e47970 |
|
•
•
•
•
•
|
| Publication |
| First Author: |
The Jackson Laboratory Backcross DNA Panel Mapping Resource |
| Year: |
1999 |
| Journal: |
Database Release |
| Title: |
JAX BSB Panel Mapping Data |
|
|
|
|
•
•
•
•
•
|
| Protein Coding Gene |
| Type: |
protein_coding_gene |
| Organism: |
Mus caroli |
|
•
•
•
•
•
|
| Protein Coding Gene |
| Type: |
protein_coding_gene |
| Organism: |
Mus caroli |
|
•
•
•
•
•
|
| Protein Coding Gene |
| Type: |
protein_coding_gene |
| Organism: |
mouse, laboratory |
|
•
•
•
•
•
|
| Protein Coding Gene |
| Type: |
protein_coding_gene |
| Organism: |
Mus caroli |
|
•
•
•
•
•
|
| Protein Coding Gene |
| Type: |
protein_coding_gene |
| Organism: |
mouse, laboratory |
|
•
•
•
•
•
|
| Protein Coding Gene |
| Type: |
protein_coding_gene |
| Organism: |
mouse, laboratory |
|
•
•
•
•
•
|
| Protein Coding Gene |
| Type: |
protein_coding_gene |
| Organism: |
mouse, laboratory |
|
•
•
•
•
•
|
| Protein Coding Gene |
| Type: |
protein_coding_gene |
| Organism: |
mouse, laboratory |
|
•
•
•
•
•
|
| Protein Coding Gene |
| Type: |
protein_coding_gene |
| Organism: |
mouse, laboratory |
|
•
•
•
•
•
|
| Protein Coding Gene |
| Type: |
protein_coding_gene |
| Organism: |
mouse, laboratory |
|
•
•
•
•
•
|
| Protein Coding Gene |
| Type: |
protein_coding_gene |
| Organism: |
mouse, laboratory |
|
•
•
•
•
•
|
| Protein Coding Gene |
| Type: |
protein_coding_gene |
| Organism: |
mouse, laboratory |
|
•
•
•
•
•
|
| Protein Coding Gene |
| Type: |
protein_coding_gene |
| Organism: |
mouse, laboratory |
|
•
•
•
•
•
|