iPTMnet Report for Q9NQQ7 (SLC35C2)


Protein Information

Cytoscape View


UniProt AC / UniProt ID Q9NQQ7 / S35C2_HUMAN
Protein Name Solute carrier family 35 member C2
Gene Name Name: SLC35C2
Synonyms:C20orf5,OVCOV1;ORFNames:CGI-15;
Organism Homo sapiens (Human)

PRO ID PR:Q9NQQ7
DAG View
PRO Name solute carrier family 35 member C2 (human)
Definition A solute carrier family 35 member C2 that is encoded in the genome of human.
Short Label hSLC35C2
Category organism-gene

Interactive Sequence View

Select/align proteoforms across species


Q9NQQ7 (SLC35C2) as Substrate



Site PTM Type PTM Enzyme Score Source PMID
S101 Phosphorylation PhosphoSitePlus
S104 Phosphorylation PhosphoSitePlus
Y107 Phosphorylation PhosphoSitePlus
S118 Phosphorylation PhosphoSitePlus
S119 Phosphorylation PhosphoSitePlus
S245 Phosphorylation IEDB 32357974
K331 Ubiquitination PhosphoSitePlus
S335 Phosphorylation phospho.ELM   PhosphoSitePlus   UniProt 18669648, 23186163
S336 Phosphorylation PhosphoSitePlus   UniProt 23186163
Y358 Phosphorylation PhosphoSitePlus
Site PTM Type PTM Enzyme Score Source PMID
T155 Phosphorylation HPRD 20068231
S335 Phosphorylation HPRD 19413330, 18578522, 20058876, ...19651622, 18669648, 20166139, 20068231
S336 Phosphorylation HPRD 18578522, 20058876, 17081983
Site PTM Type PTM Enzyme Score Source PMID
S314 Phosphorylation HPRD 19413330, 18578522, 20058876, ...19651622, 18669648, 20166139, 20068231
S315 Phosphorylation HPRD 18578522, 20058876, 17081983


PTM sites affected in variants

Site Variant Source PMID Disease [Sample source]
S104 C104 Biomuta DOID:10534 / stomach cancer [ cosmic, icgc ]
Y107 F107 Biomuta DOID:1793 / pancreatic cancer [ cosmic ]
S118 F118 Biomuta DOID:4159 / skin cancer [ cosmic, icgc ] DOID:1324 / lung cancer [ cosmic, icgc ]