GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

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

Displaying entries **3876 - 3900** of **9988** in total

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Gene ID	Gene Name ▼	Gene Symbol	Disease Ontology
4493	metallothionein 1E	MT1E
65258	metallophosphoesterase 1	MPPE1 Cdc1 PGAP5 post-GPI attachment to proteins 5	bipolar disorder borderline personality disorder cancer cerebral malaria chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma embryoma hepatitis B hepatitis influenza intermittent explosive disorder malaria melanoma papillary renal cell carcinoma pneumonia renal cell carcinoma sarcomatoid renal cell carcinoma skin melanoma
4520	metal regulatory transcription factor 1	MTF1
92140	metadherin	MTDH
326625	metabolism of cobalamin associated B	MMAB
10232	mesothelin	MSLN CAK1 MPF	acoustic neuroma adenocarcinoma adenoma adenosarcoma adult acute lymphocytic leukemia angiomatous meningioma anthracosilicosis asbestosis benign meningioma benign mesothelioma bile duct adenocarcinoma bile duct cancer bile duct carcinoma breast cancer bronchus cancer bronchus carcinoma byssinosis cancer carcinoma cerebral convexity meningioma cervical adenocarcinoma cervical cancer cervical squamous cell carcinoma cervicitis cervix carcinoma childhood leukemia cholangiocarcinoma chronic salpingo-oophoritis clear cell meningioma colorectal cancer colorectal carcinoma common bile duct neoplasm cribriform carcinoma distal arthrogryposis embryoma endocervicitis endometrial cancer endometrial carcinoma endometrial serous adenocarcinoma essential hypertension fibrous meningioma gastric adenocarcinoma giant cell glioblastoma glioblastoma gliosarcoma granular cell carcinoma hematologic cancer hepatocellular carcinoma high grade glioma hypertension intrahepatic cholangiocarcinoma intraorbital meningioma intraventricular meningioma kidney failure large intestine cancer liver cancer liver cirrhosis lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lung small cell carcinoma malignant mesothelioma malignant pleural mesothelioma meningioma meningothelial meningioma microcystic meningioma microphthalmia mixed glioma nephroblastoma obsolete Matthew-Wood syndrome olfactory groove meningioma ovarian cancer ovarian carcinoma ovary serous adenocarcinoma pancreas disease pancreatic adenocarcinoma pancreatic cancer pancreatic carcinoma pancreatic ductal adenocarcinoma pancreatic ductal carcinoma parasagittal meningioma patent ductus arteriosus pituitary adenoma psammomatous meningioma salivary gland cancer sarcomatoid carcinoma secretory meningioma spinal meningioma stomach cancer stomach carcinoma thymic carcinoma thymoma transitional meningioma tubular adenocarcinoma uterine corpus cancer
4232	mesoderm specific transcript	MEST PEG1 Paternally-expressed gene 1
23184	mesoderm development LRP chaperone	MESD
4225	meprin A subunit beta	MEP1B
4224	meprin A subunit alpha	MEP1A
83661	membrane spanning 4-domains A8	MS4A8
931	membrane spanning 4-domains A1	MS4A1
79258	membrane metalloendopeptidase like 1	MMEL1
4311	membrane metalloendopeptidase	MME
93380	membrane magnesium transporter 1	MMGT1
100127206	membrane integral NOTCH2 associated receptor 2	MINAR2
83552	membrane frizzled-related protein	MFRP
51360	membrane bound transcription factor peptidase, site 2	MBTPS2
8720	membrane bound transcription factor peptidase, site 1	MBTPS1
79143	membrane bound O-acyltransferase domain containing 7	MBOAT7 BB1 LPIAT1 LPLAT LPLAT11 hMBOA-7 lysophosphatidylinositol acyltransferase lysophosphatidylinositol acyltransferase 1 lysophospholipid acyltransferase 11 lysophospholipid acyltransferase 7	abdominal obesity-metabolic syndrome 1 adrenoleukodystrophy agnosia alcoholic hepatitis alcoholic liver cirrhosis attention deficit hyperactivity disorder autism spectrum disorder autistic disorder autosomal recessive intellectual developmental disorder 57 cardiovascular system disease cerebral degeneration choreatic disease chronic kidney disease communicating hydrocephalus depressive disorder developmental coordination disorder diabetes mellitus diabetic ketoacidosis dysthymic disorder dystonia epilepsy focal epilepsy gallbladder disease heart disease hepatitis B hepatitis C hepatitis hepatocellular carcinoma hydrocephalus intellectual disability learning disability lingual-facial-buccal dyskinesia liver cancer liver cirrhosis liver disease major depressive disorder melancholic depression microcephaly neurotic disorder obesity obsolete infantile epileptic encephalopathy obsolete melancholia obstructive hydrocephalus partial motor epilepsy senile degeneration of brain steatotic liver disease stereotypic movement disorder stomach cancer stomach carcinoma syndromic X-linked intellectual disability 94 syndromic X-linked intellectual disability type 10 type 2 diabetes mellitus visual epilepsy
129642	membrane bound O-acyltransferase domain containing 2	MBOAT2 FLJ14415 FLJ90298 LPLAT13 Lysophospholipid acyltransferase 2 lysophospholipid acyltransferase 13	adrenoleukodystrophy
154141	membrane bound O-acyltransferase domain containing 1	MBOAT1 LPEAT1 LPLAT14 MGC44669 dJ434O11.1 lysophosphatidylethanolamine acyltransferase 1 lysophospholipid acyltransferase 1 lysophospholipid acyltransferase 14	brachydactyly-syndactyly syndrome cholestasis
64844	membrane associated ring-CH-type finger 7	MARCHF7
54708	membrane associated ring-CH-type finger 5	MARCHF5
441061	membrane associated ring-CH-type finger 11	MARCHF11

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