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NHS GeneNance-Horan syndrome (congenital cataracts and dental anomalies) This gene encodes a protein containing four conserved nuclear localization signals. The encoded protein functions in eye, tooth, craniofacial and brain development, and it can regulate actin remodeling and cell morphology. Mutations in this gene have been shown to cause Nance-Horan syndrome, and also X-linked cataract-40. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, May 2014] |
NHS-AS1 GeneNHS antisense RNA 1 |
NHSL1 GeneNHS-like 1 |
NHSL2 GeneNHS-like 2 |
nhs Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term nhs in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
NHS Gene SetFrom Pathway Commons Protein-Protein Interactions interacting proteins for NHS from the Pathway Commons Protein-Protein Interactions dataset. |
nhsii Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term nhsii in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
NHSL1 Gene SetFrom NURSA Protein-Protein Interactions interacting proteins for NHSL1 from the NURSA Protein-Protein Interactions dataset. |