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GlyCosmos Genes

Integrated list of glycan-related genes extracted KEGG GENES Database, UniProt, GlycoGene Database (GGDB), Plant GARDEN and FlyGlycoDB. Glycan-related genes including glycosyltransferase, hydrolase activity (acting on glycosyl bonds), carbohydrate metabolic process, etc .

Source	Last Updated
FlyGlycoDB	March 25, 2024
GlycoGene Database (GGDB)	January 26, 2018
KEGG GENES Database	September 20, 2023
Plant GARDEN	May 28, 2020
UniProt	October 29, 2024

Selecting the function you want to look up from the categories displays a list narrowed down to glycan-related genes with that function (Gene Ontology).

Catalytic activity

glycosyltransferase activity

hydrolase activity, acting on glycosyl bonds

Binding

carbohydrate binding

Response to carbohydrate

Primary metabolic process

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

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Gene ID	Gene Name ▲	Gene Symbol	Organism	Disease Ontology
4158	melanocortin 2 receptor	MC2R	Homo sapiens (human)
112609	melanocortin 2 receptor accessory protein 2	MRAP2	Homo sapiens (human)
4159	melanocortin 3 receptor	MC3R	Homo sapiens (human)
4160	melanocortin 4 receptor	MC4R	Homo sapiens (human)
4161	melanocortin 5 receptor	MC5R	Homo sapiens (human)
4286	melanocyte inducing transcription factor	MITF	Homo sapiens (human)
4162	melanoma cell adhesion molecule	MCAM	Homo sapiens (human)
4241	melanotransferrin	MELTF Aliases: CD228 FLJ38863 MAP97 MGC4856 MTF1 MTf melanotransferrin membrane-bound transferrin-like protein	Homo sapiens (human)	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	Homo sapiens (human)
4544	melatonin receptor 1B	MTNR1B	Homo sapiens (human)
9223	membrane associated guanylate kinase, WW and PDZ domain containing 1	MAGI1	Homo sapiens (human)
55016	membrane associated ring-CH-type finger 1	MARCHF1	Homo sapiens (human)
162333	membrane associated ring-CH-type finger 10	MARCHF10	Homo sapiens (human)
441061	membrane associated ring-CH-type finger 11	MARCHF11	Homo sapiens (human)
54708	membrane associated ring-CH-type finger 5	MARCHF5	Homo sapiens (human)
64844	membrane associated ring-CH-type finger 7	MARCHF7	Homo sapiens (human)
154141	membrane bound O-acyltransferase domain containing 1	MBOAT1 Aliases: LPEAT1 LPLAT14 MGC44669 dJ434O11.1 lysophosphatidylethanolamine acyltransferase 1 lysophospholipid acyltransferase 1 lysophospholipid acyltransferase 14	Homo sapiens (human)	brachydactyly-syndactyly syndrome cholestasis
129642	membrane bound O-acyltransferase domain containing 2	MBOAT2 Aliases: FLJ14415 FLJ90298 LPLAT13 Lysophospholipid acyltransferase 2 lysophospholipid acyltransferase 13	Homo sapiens (human)	adrenoleukodystrophy
79143	membrane bound O-acyltransferase domain containing 7	MBOAT7 Aliases: BB1 LPIAT1 LPLAT LPLAT11 hMBOA-7 lysophosphatidylinositol acyltransferase lysophosphatidylinositol acyltransferase 1 lysophospholipid acyltransferase 11 lysophospholipid acyltransferase 7	Homo sapiens (human)	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	Homo sapiens (human)
51360	membrane bound transcription factor peptidase, site 2	MBTPS2	Homo sapiens (human)
83552	membrane frizzled-related protein	MFRP	Homo sapiens (human)
100127206	membrane integral NOTCH2 associated receptor 2	MINAR2	Homo sapiens (human)
93380	membrane magnesium transporter 1	MMGT1	Homo sapiens (human)
4311	membrane metalloendopeptidase	MME	Homo sapiens (human)

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