SYNGAP1 iPSC Listing Form

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Do you have a SYNGAP1 iPSC, isogenic or family control line in your lab? Are you open to sharing with academic or industry collaborators?

If so, please fill in this form and we will share the line on this page on the SRF site.

Please send any questions to info@ syngapresearchfund.org

Email *

What is the cDNA and protein-level variant? If a control is available, please create a separate entry. Please include c. and p. *

If this mutation is in clinvar or a publication, please share the link:

What type of mutation is it? *

Missense

Frameshift

Nonsense

Deletion

Other:

Donor Gender *

Male

Female

What kind of line is this? *

Patient

Control - Isogenic

Control - Parent

Control - Sibling

Other:

Where is this line housed? (Lab or Biorepository Name) *

What link should we provide for people to request this line? *

What other information would you like us to have? This will not be published.

A copy of your responses will be emailed to the address you provided.

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