Gene Ontology annotation through association of InterPro records with GO terms

Manual transfer of experimentally-verified manual GO annotation data to orthologs by curator judgment of sequence similarity

Annotation inferences using phylogenetic trees

Combined Automated Annotation using Multiple IEA Methods

DPY19L2 deletion as a major cause of globozoospermia.

A recurrent deletion of DPY19L2 causes infertility in man by blocking sperm head elongation and acrosome formation.

Proteomic characterization of the human sperm nucleus.

The secreted protein discovery initiative (SPDI), a large-scale effort to identify novel human secreted and transmembrane proteins: a bioinformatics assessment.

Complete sequencing and characterization of 21,243 full-length human cDNAs.

The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).

Duplication and relocation of the functional DPY19L2 gene within low copy repeats.

The finished DNA sequence of human chromosome 12.

Absence of Dpy19l2, a new inner nuclear membrane protein, causes globozoospermia in mice by preventing the anchoring of the acrosome to the nucleus.

C. elegans DPY-19 is a C-mannosyltransferase glycosylating thrombospondin repeats.

Distinct C-mannosylation of netrin receptor thrombospondin type 1 repeats by mammalian DPY19L1 and DPY19L3.

Topological analysis of DPY19L3, a human C-mannosyltransferase.

Genetic analyses of a large cohort of infertile patients with globozoospermia, DPY19L2 still the main actor, GGN confirmed as a guest player.

FAM209 associates with DPY19L2, and is required for sperm acrosome biogenesis and fertility in mice.

Structure, sequon recognition and mechanism of tryptophan C-mannosyltransferase.