GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

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

Displaying entries **6076 - 6100** of **9988** in total

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Gene ID	Gene Name ▲	Gene Symbol	Disease Ontology
4158	melanocortin 2 receptor	MC2R
112609	melanocortin 2 receptor accessory protein 2	MRAP2
4159	melanocortin 3 receptor	MC3R
4160	melanocortin 4 receptor	MC4R
4161	melanocortin 5 receptor	MC5R
4286	melanocyte inducing transcription factor	MITF
4162	melanoma cell adhesion molecule	MCAM
4241	melanotransferrin	MELTF CD228 FLJ38863 MAP97 MGC4856 MTF1 MTf melanotransferrin membrane-bound transferrin-like protein	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 MHC class II deficiency Pick's disease Reye syndrome Roberts syndrome Zollinger-Ellison syndrome adenosine deaminase deficiency angiomyolipoma astigmatism bone osteosarcoma cancer carcinoma central nervous system cancer cerebral degeneration cerebral primitive neuroectodermal tumor cervical cancer cervix carcinoma childhood osteosarcoma colorectal cancer colorectal carcinoma dysplastic nevus syndrome embryoma gliosarcoma high grade glioma hyperinsulinism large intestine cancer lung adenocarcinoma lung cancer medulloblastoma medulloepithelioma melanoma melanotic neuroectodermal tumor mixed glioma neuroectodermal tumor obsolete SC phocomelia syndrome obsolete embryonal Tumor with Multilayered Rosettes, C19MC-Altered osteosarcoma polycystic ovary syndrome sarcomatoid carcinoma severe combined immunodeficiency skin melanoma stomach cancer stomach carcinoma supratentorial primitive neuroectodermal tumor
4543	melatonin receptor 1A	MTNR1A
4544	melatonin receptor 1B	MTNR1B
9223	membrane associated guanylate kinase, WW and PDZ domain containing 1	MAGI1
55016	membrane associated ring-CH-type finger 1	MARCHF1
162333	membrane associated ring-CH-type finger 10	MARCHF10
441061	membrane associated ring-CH-type finger 11	MARCHF11
54708	membrane associated ring-CH-type finger 5	MARCHF5
64844	membrane associated ring-CH-type finger 7	MARCHF7
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
129642	membrane bound O-acyltransferase domain containing 2	MBOAT2 FLJ14415 FLJ90298 LPLAT13 Lysophospholipid acyltransferase 2 lysophospholipid acyltransferase 13	adrenoleukodystrophy
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
8720	membrane bound transcription factor peptidase, site 1	MBTPS1
51360	membrane bound transcription factor peptidase, site 2	MBTPS2
83552	membrane frizzled-related protein	MFRP
100127206	membrane integral NOTCH2 associated receptor 2	MINAR2
93380	membrane magnesium transporter 1	MMGT1
4311	membrane metalloendopeptidase	MME

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