Protein Information

Cytoscape View


UniProt AC / UniProt ID Q9BXS9 / S26A6_HUMAN
Protein Name Solute carrier family 26 member 6
Gene Name Name: SLC26A6
Organism Homo sapiens (Human)

PRO ID PR:Q9BXS9
DAG View
PRO Name solute carrier family 26 member 6 (human)
Definition A solute carrier family 26 member 6 that is encoded in the genome of human.
Short Label hSLC26A6
Category organism-gene

Interactive Sequence View

Select/align proteoforms across species


Q9BXS9 (SLC26A6) as Substrate



Site PTM Type PTM Enzyme Score Source PMID
K364 Ubiquitination PhosphoSitePlus
S405 Phosphorylation PhosphoSitePlus
S423 Phosphorylation PhosphoSitePlus
K535 Ubiquitination PhosphoSitePlus
S574 Phosphorylation UniProt 15990874
K587 Ubiquitination PhosphoSitePlus
S603 Phosphorylation UniProt 15990874
S616 Phosphorylation PhosphoSitePlus   UniProt 20068231
K629 Ubiquitination PhosphoSitePlus
S635 Phosphorylation PhosphoSitePlus
K638 Ubiquitination PhosphoSitePlus
K651 Ubiquitination PhosphoSitePlus
K729 Ubiquitination PhosphoSitePlus
S734 Phosphorylation HPRD   PhosphoSitePlus 19651622, 17081983, 20068231
S752 Phosphorylation PhosphoSitePlus   UniProt 17081983, 20068231
S755 Phosphorylation PhosphoSitePlus   UniProt 20068231
T757 Phosphorylation PhosphoSitePlus
Site PTM Type PTM Enzyme Score Source PMID
S616 Phosphorylation HPRD 20068231
S752 Phosphorylation HPRD 19651622, 19664994, 17081983, ...20068231
S755 Phosphorylation HPRD 19651622, 17081983, 20068231
T757 Phosphorylation HPRD 20068231
Site PTM Type PTM Enzyme Score Source PMID
S733 Phosphorylation HPRD 19651622, 19664994, 17081983, ...20068231
S736 Phosphorylation HPRD 19651622, 17081983, 20068231
T738 Phosphorylation HPRD 20068231
Site PTM Type PTM Enzyme Score Source PMID
S616 Phosphorylation HPRD 20068231
S622 Phosphorylation PhosphoSitePlus
K629 Ubiquitination PhosphoSitePlus
K637 Ubiquitination PhosphoSitePlus
S751 Phosphorylation HPRD 19651622, 19664994, 17081983, ...20068231
S754 Phosphorylation HPRD 19651622, 17081983, 20068231
T756 Phosphorylation HPRD 20068231


PTM sites affected in variants

Site Variant Source PMID Disease [Sample source]
S755 L755 Biomuta DOID:4362 / cervical cancer [ icgc, tcga ] DOID:1909 / melanoma [ tcga ]