Uniprot AC Entrez ID Gene Name Disease Cell Type PTM Type State Position PMID O76024 7466 WFS1 Autosomal dominant nonsyndromic deafness Phosphorylation N S25 O76024 7466 WFS1 Autosomal dominant nonsyndromic deafness Glycosylation N N28 O76024 7466 WFS1 Autosomal dominant nonsyndromic deafness Phosphorylation N T30 O76024 7466 WFS1 Autosomal dominant nonsyndromic deafness Phosphorylation N S32 O76024 7466 WFS1 Uterine cancer Phosphorylation N S32 O76024 7466 WFS1 Wolfram syndrome Acetylation N K108 O76024 7466 WFS1 Deafness Phosphorylation N T170 O76024 7466 WFS1 Prostate adenocarcinoma Phosphorylation N T170 O76024 7466 WFS1 Wolfram syndrome Phosphorylation N T170 O76024 7466 WFS1 Hepatocellular carcinoma Ubiquitination N K221 O76024 7466 WFS1 Autosomal dominant nonsyndromic deafness Phosphorylation N S235 O76024 7466 WFS1 Autosomal dominant nonsyndromic deafness Phosphorylation N S236 O76024 7466 WFS1 Autosomal dominant nonsyndromic deafness Phosphorylation N Y241 O76024 7466 WFS1 Stomach adenocarcinoma Ubiquitination N K252 O76024 7466 WFS1 Stomach adenocarcinoma Ubiquitination N K256 O76024 7466 WFS1 Lung adenocarcinoma Ubiquitination N K277 O76024 7466 WFS1 Ovarian serous cystadenocarcinoma Ubiquitination N K277 O76024 7466 WFS1 Testicular germ cell tumor Ubiquitination N K277 O76024 7466 WFS1 Autosomal dominant nonsyndromic deafness Glycosylation N N335 O76024 7466 WFS1 Hepatocellular carcinoma Glycosylation N N335 O76024 7466 WFS1 Transitional cell carcinoma Glycosylation N N335 O76024 7466 WFS1 Autosomal dominant nonsyndromic deafness Glycosylation N N500 O76024 7466 WFS1 Skin cutaneous melanoma Glycosylation N N500 O76024 7466 WFS1 Uterine corpus endometrial carcinoma Glycosylation N N500 O76024 7466 WFS1 Wolfram syndrome Phosphorylation N S626 O76024 7466 WFS1 Wolfram syndrome Phosphorylation N T628 O76024 7466 WFS1 Autosomal dominant nonsyndromic deafness Phosphorylation N S630 O76024 7466 WFS1 Deafness Phosphorylation N S630 O76024 7466 WFS1 Uterine corpus endometrial carcinoma Phosphorylation N S630 O76024 7466 WFS1 Wolfram syndrome Phosphorylation N S630 O76024 7466 WFS1 Autosomal dominant nonsyndromic deafness Phosphorylation N S631 O76024 7466 WFS1 Deafness Phosphorylation N S631 O76024 7466 WFS1 Uterine corpus endometrial carcinoma Phosphorylation N S631 O76024 7466 WFS1 Wolfram syndrome Phosphorylation N S631 O76024 7466 WFS1 Autosomal dominant nonsyndromic deafness Glycosylation N N661 O76024 7466 WFS1 Autosomal dominant nonsyndromic deafness Ubiquitination N K679 O76024 7466 WFS1 Lung adenocarcinoma Ubiquitination N K679 O76024 7466 WFS1 Stomach adenocarcinoma Ubiquitination N K679 O76024 7466 WFS1 Uterine corpus endometrial carcinoma Ubiquitination N K679 O76024 7466 WFS1 Wolfram-like syndrome Ubiquitination N K679 O76024 7466 WFS1 Autosomal dominant nonsyndromic deafness Glycosylation N N746 O76024 7466 WFS1 Hepatocellular carcinoma Glycosylation N N746 O76024 7466 WFS1 Autosomal dominant nonsyndromic deafness Ubiquitination N K762 O76024 7466 WFS1 Deafness Phosphorylation N T778 O76024 7466 WFS1 Wolfram syndrome Phosphorylation N T778 O76024 7466 WFS1 Wolfram-like syndrome Phosphorylation N T778 O76024 7466 WFS1 Wolfram-like syndrome Phosphorylation N S792 O76024 7466 WFS1 Wolfram-like syndrome Phosphorylation N T799 O76024 7466 WFS1 Brain lower grade glioma Ubiquitination N K800 O76024 7466 WFS1 Stomach adenocarcinoma Ubiquitination N K800 O76024 7466 WFS1 Wolfram-like syndrome Ubiquitination N K800 O76024 7466 WFS1 Autosomal dominant nonsyndromic deafness Ubiquitination N K811 O76024 7466 WFS1 Bladder urothelial carcinoma Ubiquitination N K811 O76024 7466 WFS1 Colon adenocarcinoma Ubiquitination N K811 O76024 7466 WFS1 Pancreatic adenocarcinoma Ubiquitination N K811 O76024 7466 WFS1 Stomach adenocarcinoma Ubiquitination N K811 O76024 7466 WFS1 Deafness Ubiquitination N K836 O76024 7466 WFS1 Wolfram-like syndrome Ubiquitination N K836 O76024 7466 WFS1 Wolfram-like syndrome Ubiquitination N K836