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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 **8476 - 8500** of **9988** in total

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Gene ID	Gene Name	Gene Symbol ▲	Organism	Disease Ontology
79644	steroid 5 alpha-reductase 3	SRD5A3 Aliases: 3-oxo-5-alpha-steroid 4-dehydrogenase (NADP(+)) FLJ13352 SRD5A2L SRD5A2L1 polyprenol reductase	Homo sapiens (human)	Creutzfeldt-Jakob disease Hailey-Hailey disease Kahrizi syndrome Marfan syndrome Rothmund-Thomson syndrome acquired hyperkeratosis agnosia angioma serpiginosum antithrombin III deficiency autistic disorder 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 bilateral optic nerve hypoplasia blindness capillary hemangioma cataract cavernous hemangioma cerebellar ataxia cerebellar disease coloboma congenital disorder of glycosylation Iq congenital disorder of glycosylation type I congenital disorder of glycosylation congenital hypothyroidism congenital nystagmus craniosynostosis cutis laxa dermatitis developmental coordination disorder dissociated nystagmus epilepsy eye disease fundus dystrophy glaucoma hypertrichosis hypothyroidism ichthyosis inguinal hernia intellectual disability isolated cleft palate isolated growth hormone deficiency learning disability mal de Meleda microcytic anemia microphthalmia myxedema nonepidermolytic palmoplantar keratoderma obsolete infantile epileptic encephalopathy optic atrophy palmoplantar keratosis pathologic nystagmus pituitary hypoplasia prostate cancer prostate carcinoma protein C deficiency protein S deficiency recurrent corneal erosion restrictive dermopathy situs inversus spontaneous ocular nystagmus syndromic X-linked intellectual disability 94 thrombophilia tuberous sclerosis visual epilepsy
6720	sterol regulatory element binding transcription factor 1	SREBF1	Homo sapiens (human)
6721	sterol regulatory element binding transcription factor 2	SREBF2	Homo sapiens (human)
6722	serum response factor	SRF	Homo sapiens (human)
153443	serum response factor binding protein 1	SRFBP1	Homo sapiens (human)
57522	SLIT-ROBO Rho GTPase activating protein 1	SRGAP1	Homo sapiens (human)
23380	SLIT-ROBO Rho GTPase activating protein 2	SRGAP2	Homo sapiens (human)
9901	SLIT-ROBO Rho GTPase activating protein 3	SRGAP3	Homo sapiens (human)
5552	serglycin	SRGN Aliases: PPG serglycin proteoglycan	Homo sapiens (human)	MHC class II deficiency Sertoli cell-only syndrome Y-linked spermatogenic failure 1 acute myeloid leukemia acute promyelocytic leukemia adenosine deaminase deficiency adult respiratory distress syndrome arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer candidiasis carcinoma central nervous system cancer childhood type dermatomyositis cleft palate colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congestive heart failure coronary aneurysm coronary artery disease coronary stenosis degenerative disc disease dental caries dentin caries dermatomyositis diabetes mellitus diabetic cataract diabetic retinopathy diarrhea dilated cardiomyopathy 1A dilated cardiomyopathy disease of mental health embryoma enterocele esophagus squamous cell carcinoma essential hypertension giant cell glioblastoma glioblastoma gliosarcoma glucose intolerance gynecomastia hepatitis B hepatocellular carcinoma high grade glioma hypertension infant gynecomastia isolated cleft palate large intestine cancer liver cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lupus erythematosus male infertility malignant pleural mesothelioma mixed glioma multiple myeloma nasopharynx carcinoma newborn respiratory distress syndrome nutmeg liver oligospermia oral candidiasis osteoarthritis prediabetes syndrome psychotic disorder sarcomatoid carcinoma severe combined immunodeficiency type 2 diabetes mellitus
6345	sarcalumenin	SRL	Homo sapiens (human)
6727	signal recognition particle 14	SRP14	Homo sapiens (human)
6729	signal recognition particle 54	SRP54	Homo sapiens (human)
6731	signal recognition particle 72	SRP72	Homo sapiens (human)
6733	SRSF protein kinase 2	SRPK2	Homo sapiens (human)
6734	SRP receptor subunit alpha	SRPRA	Homo sapiens (human)
58477	SRP receptor subunit beta	SRPRB	Homo sapiens (human)
8406	sushi repeat containing protein X-linked	SRPX	Homo sapiens (human)
27286	sushi repeat containing protein X-linked 2	SRPX2	Homo sapiens (human)
10250	serine and arginine repetitive matrix 1	SRRM1	Homo sapiens (human)
23524	serine/arginine repetitive matrix 2	SRRM2	Homo sapiens (human)
100170229	serine/arginine repetitive matrix 5	SRRM5	Homo sapiens (human)
51593	serrate, RNA effector molecule	SRRT	Homo sapiens (human)
10772	serine and arginine rich splicing factor 10	SRSF10	Homo sapiens (human)
9295	serine and arginine rich splicing factor 11	SRSF11	Homo sapiens (human)
135295	serine and arginine rich splicing factor 12	SRSF12	Homo sapiens (human)

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