NIH Human Embryonic Stem Cell Registry

Detailed information for selected cell line:

Cell Line: UM139-2 PGD; Fragile X Syndrome mutation
NIH Registration Number: 0292
NIH Approval Number: NIHhESC-14-0292
Available for Distribution: Yes
Provider Restrictions: None

Additional Information: UM139-2 PGD hESC line was derived from a genetically tested embryo. The line carries the genetic mutation for Fragile X Syndrome.

NIH Restrictions: (No Additional Restrictions)
Submitting Organization: University of Michigan
Provider Name: Gary D. Smith / University of Michigan
Provider Phone: 734-764-4134
Provider Email:
Provider URL:
Approval Date: 09/29/2014

View All Lines Eligible for Use

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This page last updated on October 03, 2022 
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