GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

Genes (9988) Glycans (5831) Glycoproteins (15733) Lectins (298) Pathways (2074)

Displaying entries **2476 - 2500** of **9988** in total

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Gene ID	Gene Name ▼	Gene Symbol	Disease Ontology
3767	potassium inwardly rectifying channel subfamily J member 11	KCNJ11	Parkinsonism diabetes mellitus familial hyperinsulinemic hypoglycemia 2 hyperinsulinism hypertension maturity-onset diabetes of the young type 13 permanent neonatal diabetes mellitus prediabetes syndrome sciatic neuropathy status epilepticus type 2 diabetes mellitus visual epilepsy
3758	potassium inwardly rectifying channel subfamily J member 1	KCNJ1
51133	potassium channel tetramerization domain containing 3	KCTD3
130535	potassium channel tetramerization domain containing 18	KCTD18
115207	potassium channel tetramerization domain containing 12	KCTD12
56888	potassium channel modulatory factor 1	KCMF1
157855	potassium calcium-activated channel subfamily U member 1	KCNU1
3783	potassium calcium-activated channel subfamily N member 4	KCNN4
3782	potassium calcium-activated channel subfamily N member 3	KCNN3
27345	potassium calcium-activated channel subfamily M regulatory beta subunit 4	KCNMB4
27094	potassium calcium-activated channel subfamily M regulatory beta subunit 3	KCNMB3
10242	potassium calcium-activated channel subfamily M regulatory beta subunit 2	KCNMB2
3779	potassium calcium-activated channel subfamily M regulatory beta subunit 1	KCNMB1
3778	potassium calcium-activated channel subfamily M alpha 1	KCNMA1
93210	post-GPI attachment to proteins phospholipase 3	PGAP3 CAB2 MGC9753 PER1 PP1498 post-GPI attachment to proteins 3	Cogan syndrome Crohn's colitis Crohn's disease Hirschsprung's disease Marfan syndrome Unverricht-Lundborg syndrome allergic asthma asthma bipolar disorder blepharospasm breast cancer breast carcinoma bruxism capillary disease congenital diaphragmatic hernia congenital disorder of glycosylation craniosynostosis diffuse interstitial keratitis early myoclonic encephalopathy epilepsy esotropia focal hand dystonia hereditary hemorrhagic telangiectasia hydronephrosis hyperopia hyperphosphatasia with impaired intellectual development syndrome 4 inflammatory bowel disease 1 inflammatory bowel disease intellectual disability intrinsic asthma isolated cleft palate learning disability lingual-facial-buccal dyskinesia monocular esotropia movement disease oligohydramnios scoliosis situs inversus stomach cancer stomach carcinoma syndromic X-linked intellectual disability 94 telangiectasis tuberous sclerosis ulcerative colitis visual epilepsy
80055	post-GPI attachment to proteins inositol deacylase 1	PGAP1 Bst1 FLJ12377 GPI inositol-deacylase SPG67	Burkitt lymphoma Laron syndrome achondroplasia agnosia autosomal recessive intellectual developmental disorder brain disease cerebral degeneration choreatic disease congenital disorder of glycosylation depressive disorder developmental coordination disorder dysthymic disorder dystonia epilepsy factor XII deficiency focal epilepsy fundus dystrophy holoprosencephaly 1 holoprosencephaly intellectual disability learning disability lingual-facial-buccal dyskinesia major depressive disorder melancholic depression microcephaly neurotic disorder obsolete infantile epileptic encephalopathy obsolete melancholia paroxysmal nocturnal hemoglobinuria partial motor epilepsy stereotypic movement disorder syndromic X-linked intellectual disability 94 syndromic X-linked intellectual disability type 10 visual epilepsy
84302	post-GPI attachment to proteins GalNAc transferase 4	PGAP4 MGC12992
58986	post-GPI attachment to proteins 6	PGAP6 M83
27315	post-GPI attachment to proteins 2	PGAP2 CWH43-N FGF receptor activating protein 1 FRAG1 cell wall biogenesis 43 N-terminal homolog (S. cerevisiae)	Beckwith-Wiedemann syndrome CLOVES syndrome Cogan syndrome Hirschsprung's disease Perlman syndrome Sotos syndrome Unverricht-Lundborg syndrome blepharospasm bone osteosarcoma cancer capillary disease childhood osteosarcoma cleft palate craniosynostosis diffuse interstitial keratitis early myoclonic encephalopathy embryoma esotropia focal hand dystonia hereditary hemorrhagic telangiectasia hydronephrosis hyperopia hyperphosphatasia with impaired intellectual development syndrome 3 hyperphosphatemia intellectual disability isolated cleft palate learning disability monocular esotropia oligohydramnios osteosarcoma scoliosis sensorineural hearing loss syndromic X-linked intellectual disability 94 telangiectasis visual epilepsy
64208	popeye domain cAMP effector 3	POPDC3
64091	popeye domain cAMP effector 2	POPDC2
11149	popeye domain cAMP effector 1	POPDC1
87178	polyribonucleotide nucleotidyltransferase 1	PNPT1
58155	polypyrimidine tract binding protein 2	PTBP2
5725	polypyrimidine tract binding protein 1	PTBP1

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