Csnk2A1 Foundation

Csnk2A1 Foundation company information, Employees & Contact Information

Updated May 2026

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Csnk2A1 Foundation is a Philanthropic Fundraising Services company and founded in 2018. It has approximately 11 employees on record. Contact data was last refreshed in May 2026. Find Csnk2A1 Foundation's verified employee emails, phone numbers, headquarters address, and key decision makers below.

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CSNK2A1 Foundation is focused on finding a cure for Okur-Chung Neurodevelopmental Syndrome and ensuring affected individuals have the opportunities and supports necessary for happy and full lives. CSNK2A1 Foundation is operated and funded through a committed team of volunteers, advocates and researchers. We aim to accomplish our mission by: * financing and encouraging meaningful research, * providing support to individuals affected and those that care for and love them, * promoting awareness, * educating patients, caregivers and health professionals and * advocating for issues important to our community. Okur-Chung Neurodevelopmental Syndrome is a rare genetic disorder first identified in 2016. OCNDS is caused by a mutation in the CSNK2A1 gene which is located on Chromosome 20. The gene CSNK2A1 creates a protein called CK2 which plays a crucial role in development. A mutation in this gene disrupts typical development. CSNK2A1 Foundation is a 501(c)(3) non-profit organization. EIN #82-4220939

Company Details

Employees
11
Founded
2018
Address
1929 Van Ness Ave, San Francisco,california,united States
Industry
Philanthropic Fundraising Services
NAICS
Grantmaking and Giving Services
Grantmaking Foundations
Voluntary Health Organizations
Other Grantmaking and Giving Services
Website
http://www.csnk2a1foundation.org
Keywords
San Francisco.
HQ
San Francisco, California
Competitors
National Organization for Rare Disorders, Orchard Lake Group, TSC Alliance, CACNA1A Foundation, Allen Institute, OlaWell, Tatton Brown Rahman Syndrome (TBRS) Community Inc., PACS1 Syndrome Research Foundation, YWHAG Research Foundation, Probably Genetic.
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