Calcium transporter localized to the cis- and medial-Golgi apparatus; required for protein glycosylation; GFP-fusion protein localizes to the vacuole; TMEM165, a human gene which causes Congenital Disorders of Glycosylation is orthologous and functionally complements the null allele; expression pattern and physical interactions suggest a possible role in ribosome biogenesis; expression reduced in a gcr1 null mutant [Source:SGD;Acc:S000000391]

Chromosome II: 602,634-603,476 forward strand.

This transcript has 1 exon, is annotated with 13 domains and features, is associated with 21 variant alleles and maps to 29 oligo probes.

This transcript is a product of gene YBR187W Show transcript tableHide transcript table