XB-FEAT-989658: Difference between revisions
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Human name has changed for Entrez Gene: 83861. From radial spoke 3 homolog to radial spoke head 3 homolog | Human name has changed for Entrez Gene: 83861. From radial spoke 3 homolog to radial spoke head 3 homolog | ||
05.13.19 | |||
Human name has changed for Entrez Gene: 83861. From radial spoke head 3 homolog to radial spoke head 3 | |||
=protein function= | =protein function= | ||
The protein encoded by this gene acts as a protein kinase A anchoring protein. Mutations in this gene cause primary ciliary dyskinesia; a disorder characterized by defects of the axoneme in motile cilia and sperm flagella. The homolog of this gene was first identified in the blue-green algae Chlamydomonas as encoding a radial spoke protein that formed a structural component of motile cilia and flagella. Alternate splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Dec 2016] | The protein encoded by this gene acts as a protein kinase A anchoring protein. Mutations in this gene cause primary ciliary dyskinesia; a disorder characterized by defects of the axoneme in motile cilia and sperm flagella. The homolog of this gene was first identified in the blue-green algae Chlamydomonas as encoding a radial spoke protein that formed a structural component of motile cilia and flagella. Alternate splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Dec 2016] |
Latest revision as of 10:02, 15 May 2019
rsph3
This is the community wiki page for the gene rsph3 please feel free to add any information that is relevant to this gene that is not already captured elsewhere in Xenbase.
nomenclature changes
05/21/2017 Human name has changed for Entrez Gene: 83861. From radial spoke 3 homolog to radial spoke head 3 homolog
05.13.19 Human name has changed for Entrez Gene: 83861. From radial spoke head 3 homolog to radial spoke head 3
protein function
The protein encoded by this gene acts as a protein kinase A anchoring protein. Mutations in this gene cause primary ciliary dyskinesia; a disorder characterized by defects of the axoneme in motile cilia and sperm flagella. The homolog of this gene was first identified in the blue-green algae Chlamydomonas as encoding a radial spoke protein that formed a structural component of motile cilia and flagella. Alternate splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Dec 2016]