GlyCosmos Portal

Displaying entries **51 - 75** of **358** in total

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Gene ID	Gene Name ▼	Gene Symbol	Disease Ontology
568915	polypeptide N-acetylgalactosaminyltransferase like 6	galntl6
797549	polypeptide N-acetylgalactosaminyltransferase 9	galnt9
100535692	polypeptide N-acetylgalactosaminyltransferase 8b, tandem duplicate 2	galnt8b.2
559373	polypeptide N-acetylgalactosaminyltransferase 8b, tandem duplicate 1	galnt8b.1
568500	polypeptide N-acetylgalactosaminyltransferase 8a, tandem duplicate 2	galnt8a.2
568547	polypeptide N-acetylgalactosaminyltransferase 8a, tandem duplicate 1	galnt8a.1
100334784	polypeptide N-acetylgalactosaminyltransferase 5	galnt5
567794	polypeptide N-acetylgalactosaminyltransferase 17	galnt17
103910015	polypeptide N-acetylgalactosaminyltransferase 10-like	LOC103910015
560788	poly (ADP-ribose) polymerase 1	parp1	Alzheimer's disease Huntington's disease Parkinson's disease arthritis asthma autoimmune disease bacterial meningitis borna disease congestive heart failure idiopathic pulmonary fibrosis kidney failure leiomyoma liver cirrhosis middle cerebral artery infarction nephritis perinatal necrotizing enterocolitis stomach cancer stomach carcinoma transient cerebral ischemia type 2 diabetes mellitus ureteral obstruction
100148642	phosphatidylinositol glycan anchor biosynthesis, class V	pigv	hyperphosphatasia with impaired intellectual development syndrome 1
393361	phosphatidylinositol glycan anchor biosynthesis, class M	pigm
393448	phosphatidylinositol glycan anchor biosynthesis, class B	pigb	developmental and epileptic encephalopathy 80 sleeping sickness
791759	phosphatidylinositol glycan anchor biosynthesis, class A	piga	autosomal recessive congenital ichthyosis 4B multiple congenital anomalies-hypotonia-seizures syndrome 2 paroxysmal nocturnal hemoglobinuria
100333333	mgat4 family member C	mgat4c
393526	methylthioadenosine phosphorylase	mtap	biliary tract benign neoplasm common bile duct neoplasm diaphyseal medullary stenosis with malignant fibrous histiocytoma pancreatic cancer
101884072	mannosyl (alpha-1,6-)-glycoprotein beta-1,6-N-acetyl-glucosaminyltransferase, isozyme B	mgat5b
566679	mannosidase endo-alpha like	maneal
415220	mannose-P-dolichol utilization defect 1b	mpdu1b	congenital disorder of glycosylation If
447806	mannose-P-dolichol utilization defect 1a	mpdu1a	congenital disorder of glycosylation If
557801	interleukin 1 receptor accessory protein-like 1b	il1rapl1b	intellectual disability non-syndromic X-linked intellectual disability 21
568868	interleukin 1 receptor accessory protein-like 1a	il1rapl1a	intellectual disability non-syndromic X-linked intellectual disability 21
282555	hyaluronan synthase 3	has3	pulmonary hypertension
260350	hyaluronan synthase 2	has2	diabetes insipidus middle cerebral artery infarction pulmonary hypertension
403130	hyaluronan synthase 1	has1	pulmonary hypertension

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