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Protein Coding Gene : Dnah1 dynein, axonemal, heavy chain 1

Primary Identifier  MGI:107721 Organism  mouse, laboratory
Chromosome  14 NCBI Gene Number  110084
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.1.0)

Predicted to enable dynein intermediate chain binding activity; dynein light intermediate chain binding activity; and minus-end-directed microtubule motor activity. Acts upstream of or within epithelial cilium movement involved in extracellular fluid movement and flagellated sperm motility. Located in extracellular region and sperm flagellum. Is expressed in cerebellum; choroid plexus; and lateral ventricle choroid plexus. Human ortholog(s) of this gene implicated in primary ciliary dyskinesia 37 and spermatogenic failure 18. Orthologous to human DNAH1 (dynein axonemal heavy chain 1).
PHENOTYPE: Homozygous null mice show male sterility, asthenospermia, and reduced beat frequency in tracheal cilia. Males homozygous for an ENU-induced mutation are sterile with abnormal sperm clumping behavior, asthenospermia, low in vitro fertilization rate, and impaired sperm penetration of zona pellucida. [provided by MGI curators]
  • synonyms:
  • B230373P09Rik,
  • RIKEN cDNA B230373P09 gene,
  • RIKEN cDNA E030034C22 gene,
  • MGI:2442419,
  • MGI:3038337,
  • Dnahc1,
  • E030034C22Rik,
  • MGD-MRK-36297,
  • ferf1,
  • MDHC7,
  • G1-415-19,
  • MGI:2444537,
  • dynein, axonemal, heavy chain 1,
  • Dnah1,
  • fertilization failure 1

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