GlyCosmos Portal

Danio rerio (zebrafish)

Summary

Taxonomy ID: 7955
PubChem Taxonomy: 7955

Genes (358) Glycans (175) Glycoproteins (592) Lectins (18) Pathways (252)

Displaying entries **276 - 300** of **358** in total

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Gene ID	Gene Name ▲	Gene Symbol	Disease Ontology
563570	heparan sulfate (glucosamine) 3-O-sulfotransferase 4	hs3st4
791188	heparan sulfate 2-O-sulfotransferase 1a	hs2st1a
100151174	heparan sulfate 2-O-sulfotransferase 1b	hs2st1b
553162	heparan sulfate 6-O-sulfotransferase 1a	hs6st1a	hypogonadotropic hypogonadism 15 with or without anosmia
791107	heparan sulfate 6-O-sulfotransferase 1b	hs6st1b	hypogonadotropic hypogonadism 15 with or without anosmia
378450	heparan sulfate 6-O-sulfotransferase 2	hs6st2	Paganini-Miozzo syndrome
792524	heparan sulfate 6-O-sulfotransferase 3a	hs6st3a
569353	heparan sulfate 6-O-sulfotransferase 3b	hs6st3b
403130	hyaluronan synthase 1	has1	pulmonary hypertension
260350	hyaluronan synthase 2	has2	diabetes insipidus middle cerebral artery infarction pulmonary hypertension
282555	hyaluronan synthase 3	has3	pulmonary hypertension
568868	interleukin 1 receptor accessory protein-like 1a	il1rapl1a	intellectual disability non-syndromic X-linked intellectual disability 21
557801	interleukin 1 receptor accessory protein-like 1b	il1rapl1b	intellectual disability non-syndromic X-linked intellectual disability 21
447806	mannose-P-dolichol utilization defect 1a	mpdu1a	congenital disorder of glycosylation If
415220	mannose-P-dolichol utilization defect 1b	mpdu1b	congenital disorder of glycosylation If
566679	mannosidase endo-alpha like	maneal
101884072	mannosyl (alpha-1,6-)-glycoprotein beta-1,6-N-acetyl-glucosaminyltransferase, isozyme B	mgat5b
393526	methylthioadenosine phosphorylase	mtap	biliary tract benign neoplasm common bile duct neoplasm diaphyseal medullary stenosis with malignant fibrous histiocytoma pancreatic cancer
100333333	mgat4 family member C	mgat4c
791759	phosphatidylinositol glycan anchor biosynthesis, class A	piga	autosomal recessive congenital ichthyosis 4B multiple congenital anomalies-hypotonia-seizures syndrome 2 paroxysmal nocturnal hemoglobinuria
393448	phosphatidylinositol glycan anchor biosynthesis, class B	pigb	developmental and epileptic encephalopathy 80 sleeping sickness
393361	phosphatidylinositol glycan anchor biosynthesis, class M	pigm
100148642	phosphatidylinositol glycan anchor biosynthesis, class V	pigv	hyperphosphatasia with impaired intellectual development syndrome 1
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
103910015	polypeptide N-acetylgalactosaminyltransferase 10-like	LOC103910015

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