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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 **414976 - 415000** of **422592** in total

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Gene ID ▼	Gene Name	Gene Symbol	Organism	Disease Ontology
23547	leukocyte immunoglobulin like receptor A4	LILRA4	Homo sapiens (human)
23545	ATPase H+ transporting V0 subunit a2	ATP6V0A2 Aliases: ATP6N1D ATP6a2 J6B7 RTF Stv1 TJ6 TJ6M TJ6s V-ATPase subunit a2 V-type proton ATPase 116 kDa subunit a2 Vph1 a2 a2V infantile malignant osteopetrosis regeneration and tolerance factor	Homo sapiens (human)	Crohn's colitis Crohn's disease Dandy-Walker syndrome Ehlers-Danlos syndrome Hailey-Hailey disease Joubert syndrome Laron syndrome Miller-Dieker lissencephaly syndrome Rothmund-Thomson syndrome achondroplasia agnosia alopecia aortic valve disease 1 aortic valve disease 2 aortic valve stenosis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis autosomal dominant cutis laxa 1 autosomal dominant cutis laxa 2 autosomal dominant cutis laxa 3 autosomal dominant cutis laxa autosomal recessive cutis laxa type IA autosomal recessive cutis laxa type IB autosomal recessive cutis laxa type II classic type autosomal recessive cutis laxa type IIA autosomal recessive cutis laxa type IIB autosomal recessive cutis laxa type IIC autosomal recessive cutis laxa type IID autosomal recessive cutis laxa type IIIA autosomal recessive cutis laxa type IIIB autosomal recessive osteopetrosis 1 autosomal recessive osteopetrosis 7 bacterial sepsis bicuspid aortic valve disease bone disease breast cancer breast carcinoma cancer cartilage disease clubfoot complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 congenital disorder of glycosylation Il congenital disorder of glycosylation type I congenital disorder of glycosylation congenital generalized lipodystrophy type 1 congenital generalized lipodystrophy type 2 congenital generalized lipodystrophy type 3 congenital generalized lipodystrophy type 4 connective tissue disease coronary artery disease cortical dysplasia-focal epilepsy syndrome cryptococcosis cryptorchidism cutis laxa dementia dental caries dentin caries developmental coordination disorder diabetic cataract diabetic retinopathy encephalitis encephalomyelitis epilepsy essential hypertension generalized atherosclerosis geroderma osteodysplasticum giant cell glioblastoma glioblastoma gliosarcoma high grade glioma hydranencephaly hypertension hypertropia inflammatory bowel disease 1 inflammatory bowel disease inguinal hernia intellectual disability intracranial aneurysm learning disability lipoatrophic diabetes mellitus lipodystrophy lissencephaly lung disease mal de Meleda male infertility mechanical strabismus microcephaly mixed glioma myelitis myopia omphalocele ophthalmoplegia osteogenesis imperfecta osteopetrosis osteosclerosis placental insufficiency platelet-type bleeding disorder 11 platelet-type bleeding disorder 3 platelet-type bleeding disorder 8 platelet-type bleeding disorder 9 pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 pulmonary emphysema renal tubular acidosis restrictive dermopathy scoliosis septooptic dysplasia short-rib thoracic dysplasia 14 with polydactyly status epilepticus strabismus syndromic X-linked intellectual disability Najm type ulcerative colitis umbilical hernia visual epilepsy von Willebrand's disease wrinkly skin syndrome
23544	seizure related 6 homolog like	SEZ6L	Homo sapiens (human)
23538	olfactory receptor family 52 subfamily A member 1	OR52A1	Homo sapiens (human)
23530	nicotinamide nucleotide transhydrogenase	NNT	Homo sapiens (human)
23529	cardiotrophin like cytokine factor 1	CLCF1	Homo sapiens (human)
23528	zinc finger protein 281	ZNF281	Homo sapiens (human)
23527	ArfGAP with coiled-coil, ankyrin repeat and PH domains 2	ACAP2	Homo sapiens (human)
23526	Rho GTPase activating protein 45	ARHGAP45	Homo sapiens (human)
23524	serine/arginine repetitive matrix 2	SRRM2	Homo sapiens (human)
23523	calcineurin binding protein 1	CABIN1	Homo sapiens (human)
23522	lysine acetyltransferase 6B	KAT6B	Homo sapiens (human)
23521	ribosomal protein L13a	RPL13A	Homo sapiens (human)
23518	R3H domain containing 1	R3HDM1	Homo sapiens (human)
23516	solute carrier family 39 member 14	SLC39A14	Homo sapiens (human)	hypermanganesemia with dystonia 2
23515	MORC family CW-type zinc finger 3	MORC3	Homo sapiens (human)
23513	scribble planar cell polarity protein	SCRIB	Homo sapiens (human)
23512	SUZ12 polycomb repressive complex 2 subunit	SUZ12	Homo sapiens (human)
23511	nucleoporin 188	NUP188	Homo sapiens (human)
23509	protein O-fucosyltransferase 1	POFUT1 Aliases: FUT12 GDP-fucose protein O-fucosyltransferase 1 KIAA0180 O-FUT O-Fuc-T peptide-O-fucosyltransferase	Homo sapiens (human)	Dowling-Degos disease acrodermatitis actinic keratosis acute myocardial infarction bone marrow cancer breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma chronic obstructive pulmonary disease colorectal cancer colorectal carcinoma congestive heart failure coronary artery anomaly coronary thrombosis dermatitis gallbladder disease hepatocellular carcinoma invasive ductal carcinoma large intestine cancer liver cancer liver disease lung benign neoplasm lung cancer lung carcinoma microcephaly myeloproliferative neoplasm myocardial infarction reticulate acropigmentation of Kitamura schizophrenia seborrheic keratosis silent myocardial infarction skin disease
23507	leucine rich repeat containing 8 VRAC subunit B	LRRC8B	Homo sapiens (human)
23506	BICRA like chromatin remodeling complex associated protein	BICRAL	Homo sapiens (human)
23505	transmembrane protein 131	TMEM131	Homo sapiens (human)
23504	RIMS binding protein 2	RIMBP2	Homo sapiens (human)
23503	zinc finger FYVE-type containing 26	ZFYVE26	Homo sapiens (human)

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