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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 **8451 - 8475** of **9988** in total

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Gene ID	Gene Name	Gene Symbol ▲	Organism	Disease Ontology
92369	splA/ryanodine receptor domain and SOCS box containing 4	SPSB4	Homo sapiens (human)
6708	spectrin alpha, erythrocytic 1	SPTA1	Homo sapiens (human)
6709	spectrin alpha, non-erythrocytic 1	SPTAN1	Homo sapiens (human)
6710	spectrin beta, erythrocytic	SPTB	Homo sapiens (human)
6711	spectrin beta, non-erythrocytic 1	SPTBN1	Homo sapiens (human)
6712	spectrin beta, non-erythrocytic 2	SPTBN2	Homo sapiens (human)
57731	spectrin beta, non-erythrocytic 4	SPTBN4	Homo sapiens (human)
51332	spectrin beta, non-erythrocytic 5	SPTBN5	Homo sapiens (human)
10558	serine palmitoyltransferase long chain base subunit 1	SPTLC1 Aliases: HSAN1 LCB1 SPTI hLCB1	Homo sapiens (human)	Alzheimer's disease Charcot-Marie-Tooth disease X-linked dominant 1 Charcot-Marie-Tooth disease X-linked dominant 6 Charcot-Marie-Tooth disease X-linked recessive 2 Charcot-Marie-Tooth disease X-linked recessive 3 Charcot-Marie-Tooth disease X-linked recessive 4 Charcot-Marie-Tooth disease X-linked recessive 5 Charcot-Marie-Tooth disease axonal type 2C Charcot-Marie-Tooth disease axonal type 2F Charcot-Marie-Tooth disease axonal type 2H Charcot-Marie-Tooth disease axonal type 2K Charcot-Marie-Tooth disease axonal type 2L Charcot-Marie-Tooth disease axonal type 2N Charcot-Marie-Tooth disease axonal type 2O Charcot-Marie-Tooth disease axonal type 2P Charcot-Marie-Tooth disease axonal type 2Q Charcot-Marie-Tooth disease axonal type 2T Charcot-Marie-Tooth disease axonal type 2U Charcot-Marie-Tooth disease dominant intermediate A Charcot-Marie-Tooth disease dominant intermediate B Charcot-Marie-Tooth disease dominant intermediate C Charcot-Marie-Tooth disease dominant intermediate D Charcot-Marie-Tooth disease dominant intermediate E Charcot-Marie-Tooth disease dominant intermediate F Charcot-Marie-Tooth disease recessive intermediate B Charcot-Marie-Tooth disease recessive intermediate C Charcot-Marie-Tooth disease recessive intermediate D Charcot-Marie-Tooth disease type 1A Charcot-Marie-Tooth disease type 1B Charcot-Marie-Tooth disease type 1C Charcot-Marie-Tooth disease type 1D Charcot-Marie-Tooth disease type 1E Charcot-Marie-Tooth disease type 1F Charcot-Marie-Tooth disease type 2 Charcot-Marie-Tooth disease type 2A1 Charcot-Marie-Tooth disease type 2A2A Charcot-Marie-Tooth disease type 2B1 Charcot-Marie-Tooth disease type 2B2 Charcot-Marie-Tooth disease type 2B Charcot-Marie-Tooth disease type 2D Charcot-Marie-Tooth disease type 2E Charcot-Marie-Tooth disease type 2I Charcot-Marie-Tooth disease type 2J Charcot-Marie-Tooth disease type 2R Charcot-Marie-Tooth disease type 2Y Charcot-Marie-Tooth disease type 4A Charcot-Marie-Tooth disease type 4B1 Charcot-Marie-Tooth disease type 4B2 Charcot-Marie-Tooth disease type 4B3 Charcot-Marie-Tooth disease type 4C Charcot-Marie-Tooth disease type 4D Charcot-Marie-Tooth disease type 4E Charcot-Marie-Tooth disease type 4F Charcot-Marie-Tooth disease type 4G Charcot-Marie-Tooth disease type 4H Charcot-Marie-Tooth disease type 4J Charcot-Marie-Tooth disease type 4K Charcot-Marie-Tooth disease Grn-related frontotemporal lobar degeneration with Tdp43 inclusions Horner's syndrome Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Riley-Day syndrome acquired hyperkeratosis agenesis of the corpus callosum with peripheral neuropathy alternating hemiplegia of childhood autonomic neuropathy bipolar disorder brain cancer breast cancer cancer central nervous system cancer central nervous system disease chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma dementia diabetes mellitus disease of mental health embryoma frontotemporal dementia gliosarcoma hereditary neuropathy with liability to pressure palsies hereditary sensory and autonomic neuropathy type 1 hereditary sensory and autonomic neuropathy type 1A hereditary sensory and autonomic neuropathy type 2 hereditary sensory and autonomic neuropathy type 5 hereditary sensory neuropathy type 4 hereditary sensory neuropathy high grade glioma juvenile amyotrophic lateral sclerosis type 27 keratosis mixed glioma motor peripheral neuropathy nervous system disease neurodegenerative disease neuropathy nonpapillary renal cell carcinoma obsolete hereditary motor and sensory neuropathy with agenesis of the corpus callosum papillary renal cell carcinoma peripheral nervous system disease polyneuropathy psychotic disorder renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma schizoaffective disorder schizophrenia schizophreniform disorder sensorineural hearing loss sensory peripheral neuropathy skin disease type 2 diabetes mellitus
9517	serine palmitoyltransferase long chain base subunit 2	SPTLC2 Aliases: KIAA0526 LCB2 LCB2A hLCB2a	Homo sapiens (human)	Charcot-Marie-Tooth disease X-linked dominant 1 Charcot-Marie-Tooth disease X-linked dominant 6 Charcot-Marie-Tooth disease X-linked recessive 2 Charcot-Marie-Tooth disease X-linked recessive 3 Charcot-Marie-Tooth disease X-linked recessive 4 Charcot-Marie-Tooth disease X-linked recessive 5 Charcot-Marie-Tooth disease axonal type 2C Charcot-Marie-Tooth disease axonal type 2F Charcot-Marie-Tooth disease axonal type 2H Charcot-Marie-Tooth disease axonal type 2K Charcot-Marie-Tooth disease axonal type 2L Charcot-Marie-Tooth disease axonal type 2N Charcot-Marie-Tooth disease axonal type 2O Charcot-Marie-Tooth disease axonal type 2P Charcot-Marie-Tooth disease axonal type 2Q Charcot-Marie-Tooth disease axonal type 2T Charcot-Marie-Tooth disease axonal type 2U Charcot-Marie-Tooth disease dominant intermediate A Charcot-Marie-Tooth disease dominant intermediate B Charcot-Marie-Tooth disease dominant intermediate C Charcot-Marie-Tooth disease dominant intermediate D Charcot-Marie-Tooth disease dominant intermediate E Charcot-Marie-Tooth disease dominant intermediate F Charcot-Marie-Tooth disease recessive intermediate B Charcot-Marie-Tooth disease recessive intermediate C Charcot-Marie-Tooth disease recessive intermediate D Charcot-Marie-Tooth disease type 1A Charcot-Marie-Tooth disease type 1B Charcot-Marie-Tooth disease type 1C Charcot-Marie-Tooth disease type 1D Charcot-Marie-Tooth disease type 1E Charcot-Marie-Tooth disease type 1F Charcot-Marie-Tooth disease type 2 Charcot-Marie-Tooth disease type 2A1 Charcot-Marie-Tooth disease type 2A2A Charcot-Marie-Tooth disease type 2B1 Charcot-Marie-Tooth disease type 2B2 Charcot-Marie-Tooth disease type 2B Charcot-Marie-Tooth disease type 2D Charcot-Marie-Tooth disease type 2E Charcot-Marie-Tooth disease type 2I Charcot-Marie-Tooth disease type 2J Charcot-Marie-Tooth disease type 2R Charcot-Marie-Tooth disease type 2Y Charcot-Marie-Tooth disease type 4A Charcot-Marie-Tooth disease type 4B1 Charcot-Marie-Tooth disease type 4B2 Charcot-Marie-Tooth disease type 4B3 Charcot-Marie-Tooth disease type 4C Charcot-Marie-Tooth disease type 4D Charcot-Marie-Tooth disease type 4E Charcot-Marie-Tooth disease type 4F Charcot-Marie-Tooth disease type 4G Charcot-Marie-Tooth disease type 4H Charcot-Marie-Tooth disease type 4J Charcot-Marie-Tooth disease type 4K Charcot-Marie-Tooth disease acute myocardial infarction agenesis of the corpus callosum with peripheral neuropathy anhidrosis cancer coronary thrombosis diarrhea hepatocellular carcinoma hereditary neuropathy with liability to pressure palsies hereditary sensory and autonomic neuropathy type 1 hereditary sensory and autonomic neuropathy type 1A hereditary sensory and autonomic neuropathy type 1C hereditary sensory and autonomic neuropathy type 2 hereditary sensory neuropathy hypohidrosis liver cancer motor peripheral neuropathy myocardial infarction neuropathy obsolete hereditary motor and sensory neuropathy with agenesis of the corpus callosum osteomyelitis parapsoriasis peripheral nervous system disease psoriasis pustulosis of palm and sole sensory peripheral neuropathy silent myocardial infarction teratocarcinoma
55304	serine palmitoyltransferase long chain base subunit 3	SPTLC3 Aliases: FLJ11112 LCB2B hLCB2b	Homo sapiens (human)	autosomal dominant cerebellar ataxia bacterial sepsis head and neck squamous cell carcinoma hereditary sensory and autonomic neuropathy type 1 neurodegenerative disease neuropathy peripheral nervous system disease polyneuropathy sensory peripheral neuropathy spinocerebellar ataxia type 7
171546	serine palmitoyltransferase small subunit A	SPTSSA Aliases: small subunit of serine palmitoyltransferase A ssSPTa	Homo sapiens (human)	hereditary spastic paraplegia 90A hereditary spastic paraplegia 90B
165679	serine palmitoyltransferase small subunit B	SPTSSB Aliases: ADMP androgen down regulated in mouse prostate small subunit of serine palmitoyltransferase B ssSPTb	Homo sapiens (human)	Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease
144108	SPT2 chromatin protein domain containing 1	SPTY2D1	Homo sapiens (human)
84654	spermatogenic leucine zipper 1	SPZ1	Homo sapiens (human)
6713	squalene epoxidase	SQLE Aliases: squalene monooxygenase	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 Pick's disease Reye syndrome breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer cerebral degeneration colorectal cancer colorectal carcinoma embryoma esophagus squamous cell carcinoma hepatocellular carcinoma large intestine cancer liver cancer long QT syndrome lung benign neoplasm lung cancer lung carcinoma lung squamous cell carcinoma microphthalmia neuroendocrine carcinoma neuroendocrine tumor obsolete Matthew-Wood syndrome prostate cancer prostate carcinoma sick sinus syndrome steatotic liver disease tinea corporis
58472	sulfide quinone oxidoreductase	SQOR	Homo sapiens (human)
8878	sequestosome 1	SQSTM1	Homo sapiens (human)
10011	steroid receptor RNA activator 1	SRA1	Homo sapiens (human)
55133	S1 RNA binding domain 1	SRBD1	Homo sapiens (human)
6714	SRC proto-oncogene, non-receptor tyrosine kinase	SRC	Homo sapiens (human)
10847	Snf2 related CREBBP activator protein	SRCAP	Homo sapiens (human)
80725	SRC kinase signaling inhibitor 1	SRCIN1	Homo sapiens (human)
6715	steroid 5 alpha-reductase 1	SRD5A1 Aliases: 3-oxo-5-alpha-steroid 4-dehydrogenase 1	Homo sapiens (human)	abdominal aortic aneurysm alcohol dependence alcohol use disorder alopecia androgenic alopecia anxiety disorder bipolar disorder breast cancer breast carcinoma cancer central nervous system cancer congenital hypothyroidism depressive disorder diabetes mellitus dysthymic disorder embryoma endometriosis of ovary endometriosis of uterus endometriosis generalized anxiety disorder gliosarcoma high grade glioma hyperprolactinemia hypospadias hypothyroidism intermittent claudication major depressive disorder melancholic depression mixed glioma myxedema neurotic disorder nodular prostate obesity obsolete melancholia panic disorder peripheral artery disease peripheral vascular disease phobic disorder polycystic ovary syndrome primary cutaneous amyloidosis prostate cancer prostate carcinoma prostatic adenoma prostatic hypertrophy type 2 diabetes mellitus
6716	steroid 5 alpha-reductase 2	SRD5A2 Aliases: 3-oxo-5-alpha-steroid 4-dehydrogenase 2	Homo sapiens (human)	Sertoli cell-only syndrome Turner syndrome Y-linked spermatogenic failure 1 abdominal obesity-metabolic syndrome 1 adenosarcoma alcohol dependence alcohol use disorder alopecia androgen insensitivity syndrome androgenic alopecia azoospermia breast cancer breast carcinoma cancer childhood acute lymphocytic leukemia cryptorchidism diabetes mellitus diabetic ketoacidosis disorder of sexual development embryoma endometrial cancer endometrial carcinoma endometriosis of ovary endometriosis of uterus endometriosis gallbladder disease gonadal dysgenesis hepatitis C hepatocellular carcinoma hermaphroditism hyperprolactinemia hypogonadotropic hypogonadism 23 with or without anosmia hypospadias liver cancer liver carcinoma liver disease nephroblastoma nodular prostate oligospermia ovarian cancer ovarian carcinoma pancreatitis peripheral artery disease phimosis polycystic ovary syndrome post-traumatic stress disorder prostate cancer prostate carcinoma prostate disease prostatic adenoma pseudohermaphroditism schizophrenia type 2 diabetes mellitus urinary tract obstruction uterine corpus cancer

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