Varaico: Literature-Extracted Genetic Variants

Gene:CSNK1D
Variant:p.I15N
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CSNK1D

NM_001893.6:p.I15N

Associated Papers

Discriminating activating, deactivating and resistance variants in protein kinases.

Singh G et al.

Genome Medicine, 2025

41152984 (PubMed )
Supplement: 13073_2025_1564_MOESM2_ESM.xlsx › Table_S5

Migraine in monogenic disorders: Shedding light on new therapeutic targets.

Mascarella D et al.

Cephalalgia : an International Journal of Headache, 2025

Increased presynaptic excitability in a migraine with aura mutation.

Suryavanshi P et al.

Brain : a Journal of Neurology, 2024

Genetic Mechanisms of Migraine: Insights from Monogenic Migraine Mutations.

Gosalia H et al.

International Journal of Molecular Sciences, 2023

Genetics of migraine: where are we now?

Grangeon L et al.

The Journal of Headache and Pain, 2023

Genetics of migraine: Delineation of contemporary understanding of the genetic underpinning of migraine.

de Boer I et al.

Handbook of Clinical Neurology, 2023

The impact of Mendelian sleep and circadian genetic variants in a population setting.

Weedon MN et al.

Plos Genetics, 2022

Kinase domain autophosphorylation rewires the activity and substrate specificity of CK1 enzymes.

Cullati SN et al.

Molecular Cell, 2022

Toward a Molecular Approach to Chronotype Assessment.

Biscontin A et al.

Journal of Biological Rhythms, 2022

Genetics of migraine aura: an update.

de Boer I et al.

The Journal of Headache and Pain, 2020

Structure, regulation, and (patho-)physiological functions of the stress-induced protein kinase CK1 delta (CSNK1D).

Xu P et al.

Gene, 2019

Advances in genetics of migraine.

Sutherland HG et al.

The Journal of Headache and Pain, 2019

Genetics of Migraine: Insights into the Molecular Basis of Migraine Disorders.

Sutherland HG et al.

Headache, 2017

Animal models of monogenic migraine.

Chen SP et al.

Cephalalgia : an International Journal of Headache, 2016

Genetics of human sleep behavioral phenotypes.

Hsu PK et al.

Methods in Enzymology, 2015

Tef polymorphism is associated with sleep disturbances in patients with Parkinson's disease.

Hua P et al.

Sleep Medicine, 2012

[Functional polymorphisms in clock genes and circadian rhythm sleep disorders].

Ebisawa T

Nihon Shinkei Seishin Yakurigaku Zasshi = Japanese Journal of Psychopharmacology, 2007

Circadian rhythms in the CNS and peripheral clock disorders: human sleep disorders and clock genes.

Ebisawa T

Journal of Pharmacological Sciences, 2007

Functional consequences of a CKIdelta mutation causing familial advanced sleep phase syndrome.

Xu Y et al.

Nature, 2005

Solving the mystery of human sleep schedules one mutation at a time.

Hallows WC et al.

Critical Reviews in Biochemistry and Molecular Biology, 0

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