| Type |
Details |
Score |
| Publication |
| First Author: |
Shin E |
| Year: |
2013 |
| Journal: |
Nat Commun |
| Title: |
Doublecortin-like kinase enhances dendritic remodelling and negatively regulates synapse maturation. |
| Volume: |
4 |
|
| Pages: |
1440 |
|
•
•
•
•
•
|
| Allele |
| Name: |
doublecortin-like kinase 1; targeted mutation 1.1, Joseph G Gleeson |
| Allele Type: |
Targeted |
| Attribute String: |
Null/knockout |
|
•
•
•
•
•
|
| Allele |
| Name: |
retinitis pigmentosa 1 homolog like 1; targeted mutation 1, Jian Zuo |
| Allele Type: |
Targeted |
| Attribute String: |
Null/knockout |
|
•
•
•
•
•
|
| Strain |
| Attribute String: |
congenic, transgenic, mutant strain |
|
•
•
•
•
•
|
| Genotype |
| Symbol: |
Tg(Dcx-icre/ERT2)1Mash/? |
| Background: |
involves: C57BL/6 * DBA/2 |
| Zygosity: |
ot |
| Has Mutant Allele: |
true |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Liu Q |
| Year: |
2004 |
| Journal: |
J Neurosci |
| Title: |
The retinitis pigmentosa 1 protein is a photoreceptor microtubule-associated protein. |
| Volume: |
24 |
| Issue: |
29 |
| Pages: |
6427-36 |
|
•
•
•
•
•
|
| Allele |
| Name: |
retinitis pigmentosa 1 (human); targeted mutation 1, Jian Zuo |
| Allele Type: |
Targeted |
|
|
•
•
•
•
•
|
| Genotype |
| Symbol: |
Dclk1/Dclk1 |
| Background: |
involves: 129S1/Sv * 129X1/SvJ * Black Swiss * C57BL/6 |
| Zygosity: |
hm |
| Has Mutant Allele: |
true |
|
•
•
•
•
•
|
| Genotype |
| Symbol: |
Dclk1/Dclk1<+> |
| Background: |
involves: 129S1/Sv * 129X1/SvJ * Black Swiss * C57BL/6 |
| Zygosity: |
ht |
| Has Mutant Allele: |
true |
|
•
•
•
•
•
|
| Genotype |
| Symbol: |
Rp1l1/Rp1l1 |
| Background: |
involves: 129S7/SvEvBrd |
| Zygosity: |
hm |
| Has Mutant Allele: |
true |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Kaplan A |
| Year: |
2011 |
| Journal: |
J Cell Sci |
| Title: |
Linking cytoplasmic dynein and transport of Rab8 vesicles to the midbody during cytokinesis by the doublecortin domain-containing 5 protein. |
| Volume: |
124 |
| Issue: |
Pt 23 |
| Pages: |
3989-4000 |
|
•
•
•
•
•
|
| Protein Domain |
| Type: |
Family |
| Description: |
Doublecortin domain-containing protein 1 (DCDC1), also known as DCDC5, is a member of doublecortin (DCX) family. It is a microtubule-associated protein (MAP) with stable double tandem DCX repeats of ubiquitin-like tertiary fold. DCDC1 is expressed during mitosis and is involved in coordinating late cytokinesis. DCDC1 interacts with cytoplasmic dynein and Rab8, as well as with the Rab8 nucleotide exchange factor Rabin8 []. |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Yamashita T |
| Year: |
2009 |
| Journal: |
J Neurosci |
| Title: |
Essential and synergistic roles of RP1 and RP1L1 in rod photoreceptor axoneme and retinitis pigmentosa. |
| Volume: |
29 |
| Issue: |
31 |
| Pages: |
9748-60 |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Moura DMS |
| Year: |
2020 |
| Journal: |
Front Neurosci |
| Title: |
Evidence of Progenitor Cell Lineage Rerouting in the Adult Mouse Hippocampus After Status Epilepticus. |
| Volume: |
14 |
|
| Pages: |
571315 |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Klein B |
| Year: |
2020 |
| Journal: |
Sci Rep |
| Title: |
DCX+ neuronal progenitors contribute to new oligodendrocytes during remyelination in the hippocampus. |
| Volume: |
10 |
| Issue: |
1 |
| Pages: |
20095 |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Sossey-Alaoui K |
| Year: |
1999 |
| Journal: |
Genomics |
| Title: |
DCAMKL1, a brain-specific transmembrane protein on 13q12.3 that is similar to doublecortin (DCX). |
| Volume: |
56 |
| Issue: |
1 |
| Pages: |
121-6 |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Gao J |
| Year: |
2002 |
| Journal: |
Proc Natl Acad Sci U S A |
| Title: |
Progressive photoreceptor degeneration, outer segment dysplasia, and rhodopsin mislocalization in mice with targeted disruption of the retinitis pigmentosa-1 (Rp1) gene. |
| Volume: |
99 |
| Issue: |
8 |
| Pages: |
5698-703 |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Liu J |
| Year: |
2005 |
| Journal: |
Hum Mol Genet |
| Title: |
Distinct gene expression profiles and reduced JNK signaling in retinitis pigmentosa caused by RP1 mutations. |
| Volume: |
14 |
| Issue: |
19 |
| Pages: |
2945-58 |
|
•
•
•
•
•
|
| Allele |
| Name: |
hypoxanthine phosphoribosyltransferase 1; targeted mutation 20, Elizabeth M Simpson |
| Allele Type: |
Targeted |
| Attribute String: |
Reporter |
|
•
•
•
•
•
|
| Allele |
| Name: |
transgene insertion 2, Wolfgang Wurst |
| Allele Type: |
Transgenic |
| Attribute String: |
Inducible, Recombinase |
|
•
•
•
•
•
|
| Genotype |
| Symbol: |
Rp1/Rp1 |
| Background: |
involves: 129S7/SvEvBrd |
| Zygosity: |
hm |
| Has Mutant Allele: |
true |
|
•
•
•
•
•
|
| Genotype |
| Symbol: |
Rp1/Rp1<+> |
| Background: |
involves: 129S7/SvEvBrd |
| Zygosity: |
ht |
| Has Mutant Allele: |
true |
|
•
•
•
•
•
|
| Genotype |
| Symbol: |
Rp1/Rp1 |
| Background: |
involves: 129S7/SvEvBrd * C57BL/6 |
| Zygosity: |
hm |
| Has Mutant Allele: |
true |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Puklowski A |
| Year: |
2011 |
| Journal: |
Nat Cell Biol |
| Title: |
The SCF-FBXW5 E3-ubiquitin ligase is regulated by PLK4 and targets HsSAS-6 to control centrosome duplication. |
| Volume: |
13 |
| Issue: |
8 |
| Pages: |
1004-9 |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Hu J |
| Year: |
2008 |
| Journal: |
Genes Dev |
| Title: |
WD40 protein FBW5 promotes ubiquitination of tumor suppressor TSC2 by DDB1-CUL4-ROC1 ligase. |
| Volume: |
22 |
| Issue: |
7 |
| Pages: |
866-71 |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Minoda Y |
| Year: |
2009 |
| Journal: |
Biochem Biophys Res Commun |
| Title: |
An F-box protein, FBXW5, negatively regulates TAK1 MAP3K in the IL-1beta signaling pathway. |
| Volume: |
381 |
| Issue: |
3 |
| Pages: |
412-7 |
|
•
•
•
•
•
|
| Protein Domain |
| Type: |
Family |
| Description: |
FBXW5 is a F-box protein and a DDB1-binding WD40 (DWD) protein that serves as a substrate recognition component of both SCF (SKP1-CUL1-F-box protein) and DCX (DDB1-CUL4-X-box) E3 ubiquitin-protein ligase complexes [, ]. It has also been shown to negatively regulate TAK1 MAP3K in the IL-1beta signaling pathway []. Interestingly, FBXW5 binds centriolar protein HsSAS-6 and promotes its ubiquitylation; this way FBXW5 can restrict centrosome re-duplication through degradation of HsSAS-6 []. |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Zhang J |
| Year: |
2010 |
| Journal: |
BMC Neurosci |
| Title: |
A powerful transgenic tool for fate mapping and functional analysis of newly generated neurons. |
| Volume: |
11 |
|
| Pages: |
158 |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Walker TL |
| Year: |
2007 |
| Journal: |
J Neurosci |
| Title: |
The doublecortin-expressing population in the developing and adult brain contains multipotential precursors in addition to neuronal-lineage cells. |
| Volume: |
27 |
| Issue: |
14 |
| Pages: |
3734-42 |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Saaltink DJ |
| Year: |
2020 |
| Journal: |
eNeuro |
| Title: |
Doublecortin-Like Is Implicated in Adult Hippocampal Neurogenesis and in Motivational Aspects to Escape from an Aversive Environment in Male Mice. |
| Volume: |
7 |
| Issue: |
5 |
|
|
•
•
•
•
•
|
| Strain |
| Attribute String: |
targeted mutation, mutant strain, congenic |
|
•
•
•
•
•
|
| Allele |
| Name: |
transgene insertion DC-F18, Zhi-Qi Xiong |
| Allele Type: |
Transgenic |
| Attribute String: |
Inducible, Recombinase |
|
•
•
•
•
•
|
| Allele |
| Name: |
transgene insertion DC-F30, Zhi-Qi Xiong |
| Allele Type: |
Transgenic |
| Attribute String: |
Inducible, Recombinase |
|
•
•
•
•
•
|
| Genotype |
| Symbol: |
Rp1/Rp1 |
| Background: |
involves: 129S6/SvEvTac * 129S7/SvEvBrd |
| Zygosity: |
ht |
| Has Mutant Allele: |
true |
|
•
•
•
•
•
|
| Genotype |
| Symbol: |
Hprt1/? |
| Background: |
B6.129P2(Cg)-Hprt1/Mmjax |
| Zygosity: |
ot |
| Has Mutant Allele: |
true |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Ohmae S |
| Year: |
2006 |
| Journal: |
J Biol Chem |
| Title: |
Molecular identification and characterization of a family of kinases with homology to Ca2+/calmodulin-dependent protein kinases I/IV. |
| Volume: |
281 |
| Issue: |
29 |
| Pages: |
20427-39 |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Davidson AE |
| Year: |
2013 |
| Journal: |
Hum Mutat |
| Title: |
RP1L1 variants are associated with a spectrum of inherited retinal diseases including retinitis pigmentosa and occult macular dystrophy. |
| Volume: |
34 |
| Issue: |
3 |
| Pages: |
506-14 |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Garrett L |
| Year: |
2015 |
| Journal: |
Front Behav Neurosci |
| Title: |
Conditional Reduction of Adult Born Doublecortin-Positive Neurons Reversibly Impairs Selective Behaviors. |
| Volume: |
9 |
|
| Pages: |
302 |
|
•
•
•
•
•
|
| Genotype |
| Symbol: |
Dclk1/Dclk1<+> Dcx/? |
| Background: |
involves: 129S1/Sv * 129X1/SvJ * Black Swiss * C57BL/6 |
| Zygosity: |
cx |
| Has Mutant Allele: |
true |
|
•
•
•
•
•
|
| Genotype |
| Symbol: |
Dclk1/Dclk1<+> Dcx/Dcx |
| Background: |
involves: 129S1/Sv * 129X1/SvJ * Black Swiss * C57BL/6 |
| Zygosity: |
cx |
| Has Mutant Allele: |
true |
|
•
•
•
•
•
|
| Genotype |
| Symbol: |
Dclk1/Dclk1 Dcx/? |
| Background: |
involves: 129S1/Sv * 129X1/SvJ * Black Swiss * C57BL/6 |
| Zygosity: |
cx |
| Has Mutant Allele: |
true |
|
•
•
•
•
•
|
| Genotype |
| Symbol: |
Dclk1/Dclk1 Dcx/Dcx |
| Background: |
involves: 129S1/Sv * 129X1/SvJ * Black Swiss * C57BL/6 |
| Zygosity: |
cx |
| Has Mutant Allele: |
true |
|
•
•
•
•
•
|
| Genotype |
| Symbol: |
Dclk1/Dclk1 Dcx/Dcx<+> |
| Background: |
involves: 129S1/Sv * 129X1/SvJ * Black Swiss * C57BL/6 |
| Zygosity: |
cx |
| Has Mutant Allele: |
true |
|
•
•
•
•
•
|
| Genotype |
| Symbol: |
Rp1/Rp1<+> Rp1l1/Rp1l1<+> |
| Background: |
involves: 129S7/SvEvBrd |
| Zygosity: |
cx |
| Has Mutant Allele: |
true |
|
•
•
•
•
•
|
| Genotype |
| Symbol: |
Gt(ROSA)26Sor/Gt(ROSA)26Sor<+> Tg(Dcx-icre/ERT2)1Mash/? |
| Background: |
involves: 129S6/SvEvTac * C57BL/6 * DBA/2 |
| Zygosity: |
cn |
| Has Mutant Allele: |
true |
|
•
•
•
•
•
|
| Genotype |
| Symbol: |
Gt(ROSA)26Sor/Gt(ROSA)26Sor<+> Tg(Dcx-icre/ERT2)1Mash/? |
| Background: |
involves: 129S4/SvJaeSor * C57BL/6 * DBA/2 |
| Zygosity: |
cn |
| Has Mutant Allele: |
true |
|
•
•
•
•
•
|
| Protein |
| Organism: |
Mus musculus/domesticus |
| Length: |
797
 |
| Fragment?: |
false |
|
•
•
•
•
•
|
| Protein |
| Organism: |
Mus musculus/domesticus |
| Length: |
797
 |
| Fragment?: |
false |
|
•
•
•
•
•
|
| Protein |
| Organism: |
Mus musculus/domesticus |
| Length: |
815
 |
| Fragment?: |
true |
|
•
•
•
•
•
|
| Protein |
| Organism: |
Mus musculus/domesticus |
| Length: |
764
 |
| Fragment?: |
true |
|
•
•
•
•
•
|
| Protein |
| Organism: |
Mus musculus/domesticus |
| Length: |
186
 |
| Fragment?: |
false |
|
•
•
•
•
•
|
| Protein |
| Organism: |
Mus musculus/domesticus |
| Length: |
148
 |
| Fragment?: |
false |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Nakagawa K |
| Year: |
2022 |
| Journal: |
Sci Rep |
| Title: |
Endoplasmic reticulum stress contributes to the decline in doublecortin expression in the immature neurons of mice with long-term obesity. |
| Volume: |
12 |
| Issue: |
1 |
| Pages: |
1022 |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Mensching L |
| Year: |
2019 |
| Journal: |
Int J Mol Sci |
| Title: |
Stable Adult Hippocampal Neurogenesis in Cannabinoid Receptor CB2 Deficient Mice. |
| Volume: |
20 |
| Issue: |
15 |
|
|
•
•
•
•
•
|
| Protein |
| Organism: |
Mus musculus/domesticus |
| Length: |
347
 |
| Fragment?: |
false |
|
•
•
•
•
•
|
| Protein |
| Organism: |
Mus musculus/domesticus |
| Length: |
287
 |
| Fragment?: |
false |
|
•
•
•
•
•
|
| Protein |
| Organism: |
Mus musculus/domesticus |
| Length: |
347
 |
| Fragment?: |
false |
|
•
•
•
•
•
|
| Protein |
| Organism: |
Mus musculus/domesticus |
| Length: |
622
 |
| Fragment?: |
true |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Guillonneau X |
| Year: |
1999 |
| Journal: |
Hum Mol Genet |
| Title: |
A nonsense mutation in a novel gene is associated with retinitis pigmentosa in a family linked to the RP1 locus. |
| Volume: |
8 |
| Issue: |
8 |
| Pages: |
1541-6 |
|
•
•
•
•
•
|
| Protein |
| Organism: |
Mus musculus/domesticus |
| Length: |
340
 |
| Fragment?: |
true |
|
•
•
•
•
•
|
| Protein |
| Organism: |
Mus musculus/domesticus |
| Length: |
376
 |
| Fragment?: |
false |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Sapir T |
| Year: |
2000 |
| Journal: |
Hum Mol Genet |
| Title: |
Doublecortin mutations cluster in evolutionarily conserved functional domains. |
| Volume: |
9 |
| Issue: |
5 |
| Pages: |
703-12 |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Horesh D |
| Year: |
1999 |
| Journal: |
Hum Mol Genet |
| Title: |
Doublecortin, a stabilizer of microtubules. |
| Volume: |
8 |
| Issue: |
9 |
| Pages: |
1599-610 |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Benedetti B |
| Year: |
2020 |
| Journal: |
Cereb Cortex |
| Title: |
Functional Integration of Neuronal Precursors in the Adult Murine Piriform Cortex. |
| Volume: |
30 |
| Issue: |
3 |
| Pages: |
1499-1515 |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Villasana LE |
| Year: |
2015 |
| Journal: |
eNeuro |
| Title: |
Functional Integration of Adult-Born Hippocampal Neurons after Traumatic Brain Injury(1,2,3). |
| Volume: |
2 |
| Issue: |
5 |
|
|
•
•
•
•
•
|
| Publication |
| First Author: |
Lima da Cruz RV |
| Year: |
2018 |
| Journal: |
Front Mol Neurosci |
| Title: |
A Single Dose of 5-MeO-DMT Stimulates Cell Proliferation, Neuronal Survivability, Morphological and Functional Changes in Adult Mice Ventral Dentate Gyrus. |
| Volume: |
11 |
|
| Pages: |
312 |
|
•
•
•
•
•
|
| Protein Domain |
| Type: |
Homologous_superfamily |
| Description: |
X-linked lissencephaly is a severe brain malformation affecting males. Recently it has been demonstrated that the doublecortin gene is implicated in this disorder []. Doublecortin was found to bind to the microtubule cytoskeleton. In vivo and in vitro assays show that Doublecortin stabilises microtubules and causes bundling []. Doublecortin is a basic protein with an iso-electric point of 10, typical of microtubule-binding proteins. However, its sequence contains no known microtubule-binding domain(s).The detailed sequence analysis of Doublecortin and Doublecortin-like proteins allowed the identification of an evolutionarily conserved Doublecortin (DC) domain, which is ubiquitin-like. This domain is found in the N terminus of proteins and consists of one or two tandemly repeated copies of an around 80 amino acids region. It has been suggested that the first DC domain of Doublecortin binds tubulin and enhances microtubule polymerisation [].Some proteins known to contain a DC domain are listed below:Doublecortin. It is required for neuronal migration []. A large number of point mutations in the human DCX gene leading to lissencephaly are located within the DC domains [].Human serine/threonine-protein kinase DCAMKL1. It is a probable kinase that may be involved in a calcium-signaling pathway controlling neuronal migration in the developing brain [, ].Retinitis pigmentosa 1 protein. It is required for the differentiation of photoreceptor cells. Mutation in the human RP1 gene cause retinitis pigmentosa of type 1 [, ]. |
|
•
•
•
•
•
|
| Protein Domain |
| Type: |
Domain |
| Description: |
X-linked lissencephaly is a severe brain malformation affecting males. Recently it has been demonstrated that the doublecortin gene is implicated in this disorder []. Doublecortin was found to bind to the microtubule cytoskeleton. In vivo and in vitro assays show that Doublecortin stabilises microtubules and causes bundling []. Doublecortin is a basic protein with an iso-electric point of 10, typical of microtubule-binding proteins. However, its sequence contains no known microtubule-binding domain(s).The detailed sequence analysis of Doublecortin and Doublecortin-like proteins allowed the identification of an evolutionarily conserved Doublecortin (DC) domain, which is ubiquitin-like. This domain is found in the N terminus of proteins and consists of one or two tandemly repeated copies of an around 80 amino acids region. It has been suggested that the first DC domain of Doublecortin binds tubulin and enhances microtubule polymerisation [].Some proteins known to contain a DC domain are listed below:Doublecortin. It is required for neuronal migration []. A large number of point mutations in the human DCX gene leading to lissencephaly are located within the DC domains [].Human serine/threonine-protein kinase DCAMKL1. It is a probable kinase that may be involved in a calcium-signaling pathway controlling neuronal migration in the developing brain [, ].Retinitis pigmentosa 1 protein. It is required for the differentiation of photoreceptor cells. Mutation in the human RP1 gene cause retinitis pigmentosa of type 1 [, ]. |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Bilasy SE |
| Year: |
2009 |
| Journal: |
Eur J Neurosci |
| Title: |
Dorsal telencephalon-specific RA-GEF-1 knockout mice develop heterotopic cortical mass and commissural fiber defect. |
| Volume: |
29 |
| Issue: |
10 |
| Pages: |
1994-2008 |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Pechnick RN |
| Year: |
2008 |
| Journal: |
Proc Natl Acad Sci U S A |
| Title: |
p21Cip1 restricts neuronal proliferation in the subgranular zone of the dentate gyrus of the hippocampus. |
| Volume: |
105 |
| Issue: |
4 |
| Pages: |
1358-63 |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Li X |
| Year: |
2022 |
| Journal: |
FASEB J |
| Title: |
Transient early life growth hormone exposure permanently alters brain, muscle, liver, macrophage, and adipocyte status in long-lived Ames dwarf mice. |
| Volume: |
36 |
| Issue: |
7 |
| Pages: |
e22394 |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Xiao XL |
| Year: |
2013 |
| Journal: |
Brain Res |
| Title: |
Metabotropic glutamate receptor 5 (mGluR5) regulates proliferation and differentiation of neuronal progenitors in the developmental hippocampus. |
| Volume: |
1493 |
|
| Pages: |
1-12 |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Wu MD |
| Year: |
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