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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 **412501 - 412525** of **422592** in total

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Gene ID ▼	Gene Name	Gene Symbol	Organism	Disease Ontology
51307	family with sequence similarity 53 member C	FAM53C	Homo sapiens (human)
51305	potassium two pore domain channel subfamily K member 9	KCNK9	Homo sapiens (human)
51303	FKBP prolyl isomerase 11	FKBP11	Homo sapiens (human)
51302	cytochrome P450 family 39 subfamily A member 1	CYP39A1	Homo sapiens (human)	Charcot-Marie-Tooth disease type 5 MASA syndrome Mast syndrome SPOAN syndrome Troyer syndrome agranulocytosis gallbladder cancer gallbladder carcinoma hepatocellular carcinoma hereditary spastic paraplegia 10 hereditary spastic paraplegia 11 hereditary spastic paraplegia 12 hereditary spastic paraplegia 13 hereditary spastic paraplegia 14 hereditary spastic paraplegia 15 hereditary spastic paraplegia 16 hereditary spastic paraplegia 17 hereditary spastic paraplegia 18 hereditary spastic paraplegia 19 hereditary spastic paraplegia 23 hereditary spastic paraplegia 24 hereditary spastic paraplegia 25 hereditary spastic paraplegia 26 hereditary spastic paraplegia 27 hereditary spastic paraplegia 28 hereditary spastic paraplegia 29 hereditary spastic paraplegia 2 hereditary spastic paraplegia 30 hereditary spastic paraplegia 31 hereditary spastic paraplegia 32 hereditary spastic paraplegia 34 hereditary spastic paraplegia 35 hereditary spastic paraplegia 36 hereditary spastic paraplegia 37 hereditary spastic paraplegia 38 hereditary spastic paraplegia 39 hereditary spastic paraplegia 3A hereditary spastic paraplegia 41 hereditary spastic paraplegia 42 hereditary spastic paraplegia 43 hereditary spastic paraplegia 44 hereditary spastic paraplegia 45 hereditary spastic paraplegia 46 hereditary spastic paraplegia 48 hereditary spastic paraplegia 49 hereditary spastic paraplegia 4 hereditary spastic paraplegia 53 hereditary spastic paraplegia 54 hereditary spastic paraplegia 55 hereditary spastic paraplegia 56 hereditary spastic paraplegia 57 hereditary spastic paraplegia 5A hereditary spastic paraplegia 61 hereditary spastic paraplegia 62 hereditary spastic paraplegia 63 hereditary spastic paraplegia 64 hereditary spastic paraplegia 6 hereditary spastic paraplegia 72A hereditary spastic paraplegia 73 hereditary spastic paraplegia 75 hereditary spastic paraplegia 77 hereditary spastic paraplegia 7 hereditary spastic paraplegia 8 hereditary spastic paraplegia 9A hereditary spastic paraplegia 9B hereditary spastic paraplegia leukopenia liver cancer neutropenia prostate cancer prostate carcinoma severe congenital neutropenia
51301	glucosaminyl (N-acetyl) transferase 4	GCNT4 Aliases: C2GNT3 beta-1,3-galactosyl-O-glycosyl-glycoprotein beta-1,6-N-acetylglucosaminyltransferase 4 core 2 beta-1,6-N-acetylglucosaminyltransferase 3	Homo sapiens (human)
51296	solute carrier family 15 member 3	SLC15A3	Homo sapiens (human)
51294	protocadherin 12	PCDH12	Homo sapiens (human)
51293	CD320 molecule	CD320	Homo sapiens (human)
51290	ERGIC and golgi 2	ERGIC2	Homo sapiens (human)
51289	relaxin family peptide receptor 3	RXFP3	Homo sapiens (human)
51286	cell cycle exit and neuronal differentiation 1	CEND1	Homo sapiens (human)
51284	toll like receptor 7	TLR7	Homo sapiens (human)
51283	bifunctional apoptosis regulator	BFAR	Homo sapiens (human)
51280	golgi membrane protein 1	GOLM1	Homo sapiens (human)
51279	complement C1r subcomponent like	C1RL	Homo sapiens (human)
51271	ubiquitin associated protein 1	UBAP1	Homo sapiens (human)
51267	C-type lectin domain family 1 member A	CLEC1A Aliases: CLEC-1 CLEC1 MGC34328	Homo sapiens (human)	aspergillosis black piedra coccidioidomycosis histoplasmosis sporotrichosis superficial mycosis white piedra
51266	C-type lectin domain family 1 member B	CLEC1B Aliases: CLEC-2 CLEC2	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 Evans' syndrome Marfan syndrome Pick's disease Reye syndrome adult respiratory distress syndrome androgen insensitivity syndrome arteriosclerotic cardiovascular disease atherosclerosis atrioventricular septal defect autoimmune thrombocytopenic purpura bacterial sepsis blood coagulation disease cancer cerebral degeneration cerebral infarction cerebrovascular disease chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma coronary artery disease diabetes mellitus diabetic ketoacidosis embryoma gallbladder disease hematopoietic system disease hemolytic-uremic syndrome hepatocellular carcinoma liver cancer liver disease lung benign neoplasm melanoma newborn respiratory distress syndrome nonpapillary renal cell carcinoma nutmeg liver obsolete inherited blood coagulation disease papillary renal cell carcinoma pneumonia renal carcinoma renal cell carcinoma rheumatoid arthritis sarcomatoid renal cell carcinoma situs inversus skin melanoma split hand-foot malformation 1 stomach cancer stomach carcinoma thrombocytopenia due to platelet alloimmunization thrombocytopenia thrombophilia thrombotic thrombocytopenic purpura tuberous sclerosis type 2 diabetes mellitus viral infectious disease
51264	mitochondrial ribosomal protein L27	MRPL27	Homo sapiens (human)
51246	shisa family member 5	SHISA5	Homo sapiens (human)
51232	cysteine rich transmembrane BMP regulator 1	CRIM1	Homo sapiens (human)
51231	VRK serine/threonine kinase 3	VRK3	Homo sapiens (human)
51228	glycolipid transfer protein	GLTP	Homo sapiens (human)	colon carcinoma colorectal cancer colorectal carcinoma hepatitis C large intestine cancer
51227	phosphatidylinositol glycan anchor biosynthesis class P	PIGP Aliases: DCRC DSRC phosphatidylinositol-n-acetylglucosaminyltranferase subunit P	Homo sapiens (human)	Down syndrome Joubert syndrome Marfan syndrome Miller-Dieker lissencephaly syndrome Unverricht-Lundborg syndrome West syndrome aromatase excess syndrome basal ganglia disease blepharospasm cleft palate complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 cortical dysplasia-focal epilepsy syndrome developmental and epileptic encephalopathy 1 developmental and epileptic encephalopathy 55 dystonia early infantile epileptic encephalopathy early myoclonic encephalopathy epilepsy episodic ataxia focal hand dystonia hydranencephaly hypertropia intellectual disability isolated cleft palate learning disability lingual-facial-buccal dyskinesia lissencephaly mechanical strabismus microcephaly obsolete infantile epileptic encephalopathy omphalocele ophthalmoplegia pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 prostate cancer prostate carcinoma renal agenesis septooptic dysplasia short-rib thoracic dysplasia 14 with polydactyly situs inversus strabismus syndromic X-linked intellectual disability Najm type tuberous sclerosis umbilical hernia ureterocele ventricular septal defect visual cortex disease visual epilepsy
51224	elongin A2	ELOA2	Homo sapiens (human)

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