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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 **418426 - 418450** of **422592** in total

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Gene ID ▼	Gene Name	Gene Symbol	Organism	Disease Ontology
9806	SPARC (osteonectin), cwcv and kazal like domains proteoglycan 2	SPOCK2	Homo sapiens (human)
9801	mitochondrial ribosomal protein L19	MRPL19	Homo sapiens (human)
9797	TatD DNase domain containing 2	TATDN2	Homo sapiens (human)
9796	phytanoyl-CoA 2-hydroxylase interacting protein	PHYHIP	Homo sapiens (human)
9794	mastermind like transcriptional coactivator 1	MAML1	Homo sapiens (human)
9793	cytoskeleton associated protein 5	CKAP5	Homo sapiens (human)
9792	SERTA domain containing 2	SERTAD2	Homo sapiens (human)
9791	phosphatidylserine synthase 1	PTDSS1 Aliases: KIAA0024 PSS1 PSSA	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 Bell's palsy Hailey-Hailey disease Laron syndrome Lenz-Majewski hyperostotic dwarfism Pick's disease Reye syndrome Rothmund-Thomson syndrome achondroplasia aortic disease aortic valve disease 2 aortic valve stenosis autistic disorder autosomal dominant cutis laxa 1 autosomal dominant cutis laxa 2 autosomal dominant cutis laxa 3 autosomal dominant cutis laxa autosomal dominant osteopetrosis 2 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 7 cerebral degeneration choanal atresia communicating hydrocephalus cryptorchidism cutis laxa dental enamel hypoplasia facial nerve disease facial paralysis humeroradial synostosis hydrocephalus hypogonadism hypospadias inguinal hernia intellectual disability lateral meningocele syndrome learning disability mal de Meleda obstructive hydrocephalus osteopetrosis osteosclerosis placental insufficiency priapism restrictive dermopathy scoliosis senile degeneration of brain sensorineural hearing loss syndactyly tongue disease
9790	BMS1 ribosome biogenesis factor	BMS1	Homo sapiens (human)
9789	signal peptidase complex subunit 2	SPCS2	Homo sapiens (human)
9788	MTSS I-BAR domain containing 1	MTSS1	Homo sapiens (human)
9787	DLG associated protein 5	DLGAP5	Homo sapiens (human)
9785	DEAH-box helicase 38	DHX38	Homo sapiens (human)
9784	sorting nexin 17	SNX17	Homo sapiens (human)
9782	matrin 3	MATR3	Homo sapiens (human)
9780	piezo type mechanosensitive ion channel component 1 (Er blood group)	PIEZO1	Homo sapiens (human)
9779	TBC1 domain family member 5	TBC1D5	Homo sapiens (human)
9778	KIAA0232	KIAA0232	Homo sapiens (human)
9776	autophagy related 13	ATG13	Homo sapiens (human)
9775	eukaryotic translation initiation factor 4A3	EIF4A3	Homo sapiens (human)
9774	BCL2 associated transcription factor 1	BCLAF1	Homo sapiens (human)
9772	transmembrane protein 94	TMEM94	Homo sapiens (human)
9768	PCNA clamp associated factor	PCLAF	Homo sapiens (human)
9765	zinc finger FYVE-type containing 16	ZFYVE16	Homo sapiens (human)
9762	leucine zipper tumor suppressor family member 3	LZTS3	Homo sapiens (human)

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