Nhs 抗体
(Nance-Horan Syndrome (Congenital Cataracts and Dental Anomalies) (Nhs))
This gene encodes a protein containing four conserved nuclear localization signals. The encoded protein may function during the development of the eyes, teeth, and brain. Mutations in this gene have been shown to cause Nance-Horan syndrome. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Oct 2008].
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Nhs 抗体
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Synonyms and alternative names related to Nhs
NHS actin remodeling regulator (NHS), CTRCT40, CXN, SCML1Protein level used designations for Nhs
- Nance-Horan syndrome protein
- congenital cataracts and dental anomalies protein
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