Derivation of iPSC line UMi029-A bearing a hearing-loss associated variant in the SMPX gene

Derek M. Dykxhoorn, Xiaoying Tong, Nicholas C. Gosstola, Xue Zhong Liu

Research output: Contribution to journalArticlepeer-review

Abstract

Hereditary hearing loss (HL) is the most common sensory disorder with multiple potential modes of inheritance, such as X-linked. Multiple loci have been associated with X-linked HL, including variants in the Small Muscle Protein X-Linked (SMPX) gene responsible for deafness, X-linked 4 (DFNX4) (OMIM 300066). Here we describe the derivation of an induced pluripotent stem cell (iPSC) line from an individual bearing a novel splice variant (c.133–1 G > A) that leads to a frameshift creating a premature stop codon (p.(Gly45Val*36)) in SMPX[1].

Original languageEnglish (US)
Article number102405
JournalStem Cell Research
Volume54
DOIs
StatePublished - Jul 2021

ASJC Scopus subject areas

  • Developmental Biology
  • Cell Biology

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