Also known as CILD3, DNAHC5, HL1, KTGNR, PCD, dynein axonemal heavy chain 5
Dynein axonemal heavy chain 5 is a protein that in humans is encoded by the DNAH5 gene.
This gene encodes a dynein protein, which is part of a microtubule-associated motor protein complex consisting of heavy, light, and intermediate chains. This protein is an axonemal heavy chain dynein. It functions as a force-generating protein with ATPase activity, whereby the release of ADP is thought to produce the force-producing power stroke. Mutations in this gene cause primary ciliary dyskinesia type 3, as well as Kartagener syndrome, which are both diseases due to ciliary defects. [provided by RefSeq, Oct 2009].
via MyGene.info
Dynein axonemal heavy chain 5 is a protein that in humans is encoded by the DNAH5 gene.
DNAH5 is a protein-coding gene.1 It provides the instructions for synthesizing a protein that belongs to a microtubule-associated protein complex made of heavy, light and intermediate chains.2 DNAH5 is responsible for making the heavy chain 5, found within the outer dynein arms of cilia.1 It will function as a force generating protein by using ATP, producing the power stroke for cilia.3
Discovered by embedding cosine similarity (sentence-transformers MiniLM, 384-dim).