GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

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

Displaying entries **4801 - 4825** of **9988** in total

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Gene ID	Gene Name	Gene Symbol ▼	Disease Ontology
54456	Mov10 like RNA helicase 1	MOV10L1
4343	Mov10 RNA helicase	MOV10
730094	modulator of smoothened	MOSMO
9643	mortality factor 4 like 2	MORF4L2
23515	MORC family CW-type zinc finger 3	MORC3
22880	MORC family CW-type zinc finger 2	MORC2 AC004542.C22.1 KIAA0852 ZCW3
27136	MORC family CW-type zinc finger 1	MORC1
84315	MON1 homolog A, secretory trafficking associated	MON1A
7841	mannosyl-oligosaccharide glucosidase	MOGS CWH41 DER7 GCS1 glucosidase I processing A-glucosidase I	Japanese encephalitis Turner syndrome Zika fever acquired hyperkeratosis actinic keratosis acute lymphoblastic leukemia acute myeloid leukemia adamantinoma agammaglobulinemia ameloblastoma blepharophimosis bronchus cancer bronchus carcinoma cancer cerebral degeneration chronic monocytic leukemia chronic myelomonocytic leukemia congenital disorder of glycosylation In congenital disorder of glycosylation Iq congenital disorder of glycosylation type I congenital disorder of glycosylation type II congenital disorder of glycosylation type IIb congenital disorder of glycosylation cystic fibrosis dengue disease epilepsy gonadal dysgenesis holoprosencephaly 1 holoprosencephaly juvenile myelomonocytic leukemia keratoacanthoma lung benign neoplasm lung cancer lung carcinoma lymphoblastic lymphoma malaria melanoma obesity optic atrophy pleomorphic xanthoastrocytoma sensorineural hearing loss skin melanoma viral infectious disease visual epilepsy yellow fever
346606	monoacylglycerol O-acyltransferase 3	MOGAT3 DC7 DGAT2L2 MGAT3	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Pick's disease Reye syndrome cerebral degeneration steatotic liver disease
80168	monoacylglycerol O-acyltransferase 2	MOGAT2 DGAT2L5 FLJ22644 MGAT2	diabetes mellitus diabetic ketoacidosis disease of metabolism glucose intolerance hepatocellular carcinoma liver cancer prediabetes syndrome type 2 diabetes mellitus
116255	monoacylglycerol O-acyltransferase 1	MOGAT1 DGAT2L MGAT1	multiple sclerosis overnutrition steatotic liver disease
4340	myelin oligodendrocyte glycoprotein	MOG
55034	molybdenum cofactor sulfurase	MOCOS
25843	MOB family member 4, phocein	MOB4
3110	motor neuron and pancreas homeobox 1	MNX1
4335	MAX network transcriptional repressor	MNT
4332	myeloid cell nuclear differentiation antigen	MNDA
84057	meiotic nuclear divisions 1	MND1
4330	MN1 proto-oncogene, transcriptional regulator	MN1
4594	methylmalonyl-CoA mutase	MMUT MCM	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Creutzfeldt-Jakob disease Kallmann syndrome Pick's disease Reye syndrome Sheehan syndrome acoustic neuroma actinic keratosis acute pancreatitis adult medulloblastoma adult oligodendroglioma agranulocytosis ampulla of Vater carcinoma anemia angiomatous meningioma atrial heart septal defect 1 atrial heart septal defect 2 atrial heart septal defect 3 atrial heart septal defect 4 atrial heart septal defect 5 atrial heart septal defect 6 atrial heart septal defect 7 atrial heart septal defect 8 atrial heart septal defect 9 atrial heart septal defect bacterial sepsis basal cell carcinoma basal ganglia disease benign meningioma blepharospasm bone osteosarcoma branched-chain keto acid dehydrogenase kinase deficiency breast cancer bronchus cancer bronchus carcinoma bulbar polio cancer cardiomyopathy cataract 40 central nervous system cancer cerebral convexity meningioma cerebral degeneration cerebral infarction cerebrovascular disease cervical adenocarcinoma cervical cancer cervix carcinoma cervix disease cervix uteri carcinoma in situ childhood medulloblastoma childhood oligodendroglioma childhood osteosarcoma chromophobe renal cell carcinoma clear cell meningioma clear cell renal cell carcinoma collecting duct carcinoma colon carcinoma colorectal cancer colorectal carcinoma congestive heart failure conversion disorder diabetes mellitus diabetic ketoacidosis dilated cardiomyopathy 1A dilated cardiomyopathy disease of metabolism dissociative disorder dystonia embryoma endomyocardial fibrosis epilepsy familial retinoblastoma fibrous meningioma focal hand dystonia giant cell glioblastoma glioblastoma gliosarcoma hepatocellular carcinoma high grade glioma homocystinuria hypertrophic cardiomyopathy hypogonadotropic hypogonadism 1 with or without anosmia hypogonadotropic hypogonadism 10 with or without anosmia hypogonadotropic hypogonadism 11 with or without anosmia hypogonadotropic hypogonadism 12 with or without anosmia hypogonadotropic hypogonadism 13 with or without anosmia hypogonadotropic hypogonadism 14 with or without anosmia hypogonadotropic hypogonadism 16 with or without anosmia hypogonadotropic hypogonadism 17 with or without anosmia hypogonadotropic hypogonadism 18 with or without anosmia hypogonadotropic hypogonadism 19 with or without anosmia hypogonadotropic hypogonadism 2 with or without anosmia hypogonadotropic hypogonadism 20 with or without anosmia hypogonadotropic hypogonadism 21 with or without anosmia hypogonadotropic hypogonadism 22 with or without anosmia hypogonadotropic hypogonadism 3 with or without anosmia hypogonadotropic hypogonadism 4 with or without anosmia hypogonadotropic hypogonadism 5 with or without anosmia hypogonadotropic hypogonadism 6 with or without anosmia hypogonadotropic hypogonadism 7 with or without anosmia hypogonadotropic hypogonadism 8 with or without anosmia hypogonadotropic hypogonadism 9 with or without anosmia hypogonadotropic hypogonadism hypopituitarism in situ carcinoma influenza inherited metabolic disorder intellectual disability interstitial nephritis intraorbital meningioma intraventricular meningioma inverted follicular keratosis isolated growth hormone deficiency type IA isolated growth hormone deficiency type IB isolated growth hormone deficiency type II isolated growth hormone deficiency type III isolated growth hormone deficiency keratoacanthoma kidney failure large intestine cancer laryngeal squamous cell carcinoma learning disability leukopenia liver cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma macrocytic anemia mal de Meleda medulloblastoma medullomyoblastoma melanoacanthoma melanotic medulloblastoma meningioma meningothelial meningioma methylmalonic acidemia cblA type methylmalonic acidemia cblB type methylmalonic acidemia due to transcobalamin receptor defect methylmalonic acidemia methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency microcystic meningioma microphthalmia mitochondrial metabolism disease mixed glioma mixed oligodendroglioma-astrocytoma nasopharynx carcinoma neuroblastoma neutropenia nonpapillary renal cell carcinoma obesity obsolete Matthew-Wood syndrome olfactory groove meningioma oligodendroglioma optic atrophy osteosarcoma palmoplantar keratosis pancreatic cancer pancreatic carcinoma pancreatic ductal adenocarcinoma pancreatitis pancytopenia panhypopituitarism papillary adenocarcinoma papillary renal cell carcinoma parasagittal meningioma patent foramen ovale penis carcinoma in situ pituitary adenoma poliomyelitis primary immunodeficiency disease propionic acidemia psammomatous meningioma pyelonephritis renal carcinoma renal cell carcinoma renal infectious disease retinoblastoma sarcomatoid renal cell carcinoma seborrheic keratosis secretory meningioma severe congenital neutropenia skin disease skin squamous cell carcinoma spinal meningioma stomach cancer stomach carcinoma syndactyly thrombocytopenia thyroid gland anaplastic carcinoma thyroid gland papillary carcinoma transcobalamin II deficiency transitional cell carcinoma transitional meningioma trilateral retinoblastoma tropical sprue tuberculosis urea cycle disorder visual epilepsy
79812	multimerin 2	MMRN2
22915	multimerin 1	MMRN1
4318	matrix metallopeptidase 9	MMP9
4317	matrix metallopeptidase 8	MMP8

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