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.
R64-1-1:BK006936.2
This gene has 1 transcript (splice variant) and 359 orthologues.
Name | Transcript ID | bp | Protein | Translation ID | Biotype | UniProt | RefSeq | Flags |
---|---|---|---|---|---|---|---|---|
GDT1 | YBR187W_mRNA | 843 | 280aa | YBR187W | Protein coding | P38301 | - | Ensembl Canonical, |