Gene Ontology annotation through association of InterPro records with GO terms

Annotation inferences using phylogenetic trees

Gene Ontology annotation based on UniProtKB/Swiss-Prot Subcellular Location vocabulary mapping, accompanied by conservative changes to GO terms applied by UniProt

Electronic Gene Ontology annotations created by ARBA machine learning models

DNAH3 deficiency causes flagellar inner dynein arm loss and male infertility in humans and mice.

DNAH6 and Its Interactions with PCD Genes in Heterotaxy and Primary Ciliary Dyskinesia.

Identification of DNAH6 mutations in infertile men with multiple morphological abnormalities of the sperm flagella.

Novel variants in DNAH6 cause male infertility associated with multiple morphological abnormalities of the sperm flagella (MMAF) and ICSI outcomes.

A novel frameshift mutation in DNAH6 associated with male infertility and asthenoteratozoospermia.

Patients with mutations in DNAH2, DNAH6 and DNAH10 causing multiple morphological abnormalities of human sperm flagella achieve good ICSI outcomes.

DNAH6 is a novel candidate gene associated with sperm head anomaly.

A familial study of azoospermic men identifies three novel causative mutations in three new human azoospermia genes.

Primary Ciliary Dyskinesia Associated Disease-Causing Variants in CCDC39 and CCDC40 Cause Axonemal Absence of Inner Dynein Arm Heavy Chains DNAH1, DNAH6, and DNAH7.

Axonemal structures reveal mechanoregulatory and disease mechanisms.

UniProt entry Q9C0G6 (DNAH6)