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Search results 1 to 23 out of 23 for Gyg

0.019s
Type Details Score
Gene
Type: gene
Organism: goat
Gene
Type: gene
Organism: rabbit, European
Protein
Organism: Mus musculus/domesticus
Length: 333  
Fragment?: false
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Domain
Type: Family
Description: The YobH-like protein family includes the YobH protein from E. coli , which is functionally uncharacterised. Proteins in this family are approximately 80 amino acids in length and contain two conserved sequence motifs: GYG and GLGL.
Allele
Name: potassium voltage-gated channel, subfamily Q, member 5; targeted mutation 1.1, Thomas J Jentsch
Allele Type: Targeted
Attribute String: Dominant negative
Publication
First Author: Tzingounis AV
Year: 2010
Journal: Proc Natl Acad Sci U S A
Title: The KCNQ5 potassium channel mediates a component of the afterhyperpolarization current in mouse hippocampus.
Volume: 107
Issue: 22
Pages: 10232-7
Strain
Attribute String: mutant stock, targeted mutation
Allele
Name: potassium voltage-gated channel, subfamily Q, member 4; targeted mutation 1.2, Thomas J Jentsch
Allele Type: Targeted
Attribute String: Dominant negative
Genotype
Symbol: Kcnq5/Kcnq5
Background: involves: 129S2/SvPas
Zygosity: hm
Has Mutant Allele: true
Genotype
Symbol: Kcnq4/Kcnq4<+>
Background: involves: 129/Sv * C57BL/6
Zygosity: ht
Has Mutant Allele: true
Genotype
Symbol: Kcnq4/Kcnq4
Background: involves: 129/Sv * C57BL/6
Zygosity: hm
Has Mutant Allele: true
Publication  
First Author: Fidzinski P
Year: 2015
Journal: Nat Commun
Title: KCNQ5 K(+) channels control hippocampal synaptic inhibition and fast network oscillations.
Volume: 6
Pages: 6254
Publication
First Author: Cang C
Year: 2015
Journal: Cell
Title: TMEM175 Is an Organelle K(+) Channel Regulating Lysosomal Function.
Volume: 162
Issue: 5
Pages: 1101-12
Publication
First Author: Testoni G
Year: 2017
Journal: Cell Metab
Title: Lack of Glycogenin Causes Glycogen Accumulation and Muscle Function Impairment.
Volume: 26
Issue: 1
Pages: 256-266.e4
Publication
First Author: Kharkovets T
Year: 2006
Journal: EMBO J
Title: Mice with altered KCNQ4 K+ channels implicate sensory outer hair cells in human progressive deafness.
Volume: 25
Issue: 3
Pages: 642-52
Publication
First Author: Heidenreich M
Year: 2011
Journal: Nat Neurosci
Title: KCNQ4 K(+) channels tune mechanoreceptors for normal touch sensation in mouse and man.
Volume: 15
Issue: 1
Pages: 138-45
Publication
First Author: Silverman SK
Year: 1996
Journal: Proc Natl Acad Sci U S A
Title: A regenerative link in the ionic fluxes through the weaver potassium channel underlies the pathophysiology of the mutation.
Volume: 93
Issue: 26
Pages: 15429-34
Publication
First Author: Rajan S
Year: 2000
Journal: J Biol Chem
Title: TASK-3, a novel tandem pore domain acid-sensitive K+ channel. An extracellular histiding as pH sensor.
Volume: 275
Issue: 22
Pages: 16650-7
Publication
First Author: McLerie M
Year: 2003
Journal: J Mol Cell Cardiol
Title: Dominant-negative suppression of I(K1) in the mouse heart leads to altered cardiac excitability.
Volume: 35
Issue: 4
Pages: 367-78
Publication
First Author: Spitzmaul G
Year: 2013
Journal: J Biol Chem
Title: Vestibular role of KCNQ4 and KCNQ5 K+ channels revealed by mouse models.
Volume: 288
Issue: 13
Pages: 9334-44
Publication
First Author: Schleifenbaum J
Year: 2014
Journal: Circ Res
Title: Stretch-activation of angiotensin II type 1a receptors contributes to the myogenic response of mouse mesenteric and renal arteries.
Volume: 115
Issue: 2
Pages: 263-72
Publication
First Author: Dobler T
Year: 2007
Journal: J Physiol
Title: TRESK two-pore-domain K+ channels constitute a significant component of background potassium currents in murine dorsal root ganglion neurones.
Volume: 585
Issue: Pt 3
Pages: 867-79