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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 **412626 - 412650** of **422592** in total

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Gene ID ▼	Gene Name	Gene Symbol	Organism	Disease Ontology
50839	taste 2 receptor member 10	TAS2R10	Homo sapiens (human)
50838	taste 2 receptor member 13	TAS2R13	Homo sapiens (human)
50837	taste 2 receptor member 7	TAS2R7	Homo sapiens (human)
50836	taste 2 receptor member 8	TAS2R8	Homo sapiens (human)
50835	taste 2 receptor member 9	TAS2R9	Homo sapiens (human)
50834	taste 2 receptor member 1	TAS2R1	Homo sapiens (human)
50833	taste 2 receptor member 16	TAS2R16	Homo sapiens (human)
50832	taste 2 receptor member 4	TAS2R4	Homo sapiens (human)
50831	taste 2 receptor member 3	TAS2R3	Homo sapiens (human)
50814	NAD(P) dependent steroid dehydrogenase-like	NSDHL Aliases: H105e3 SDR31E1 XAP104 short chain dehydrogenase/reductase family 31E, member 1	Homo sapiens (human)	Bloch-Sulzberger syndrome CHILD syndrome CK syndrome Joubert syndrome Miller-Dieker lissencephaly syndrome Potter's syndrome Sjogren-Larsson syndrome X-linked chondrodysplasia punctata 1 X-linked chondrodysplasia punctata 2 acquired hyperkeratosis autosomal dominant chondrodysplasia punctata autosomal recessive congenital ichthyosis bilateral renal aplasia cancer chondrodysplasia punctata cleft lip complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 cortical dysplasia-focal epilepsy syndrome cutaneous fibrous histiocytoma epidermal nevus epilepsy granuloma annulare head and neck squamous cell carcinoma heart septal defect hidradenoma hydranencephaly hydronephrosis hypertropia hypomelanosis of Ito intellectual disability learning disability lissencephaly mechanical strabismus microcephaly obsolete congenital ichthyosiform erythroderma omphalocele ophthalmoplegia pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 rhizomelic chondrodysplasia punctata type 1 rhizomelic chondrodysplasia punctata type 2 rhizomelic chondrodysplasia punctata type 3 scoliosis septooptic dysplasia short-rib thoracic dysplasia 14 with polydactyly skin papilloma skin tag strabismus syndromic X-linked intellectual disability Najm type syringoma umbilical hernia ventricular septal defect verruciform xanthoma of skin visual epilepsy
50810	HDGF like 3	HDGFL3	Homo sapiens (human)
50809	heterochromatin protein 1 binding protein 3	HP1BP3	Homo sapiens (human)
50808	adenylate kinase 3	AK3	Homo sapiens (human)
50807	ArfGAP with SH3 domain, ankyrin repeat and PH domain 1	ASAP1	Homo sapiens (human)
50801	potassium two pore domain channel subfamily K member 4	KCNK4	Homo sapiens (human)
50799	solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 13	Slc25a13	Mus musculus (house mouse)	adult-onset type II citrullinemia citrullinemia common bile duct disease intrahepatic cholestasis neonatal-onset type II citrullinemia
50798	glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase	Gne	Mus musculus (house mouse)	GNE myopathy sialuria
50796	doublesex and mab-3 related transcription factor 1	Dmrt1	Mus musculus (house mouse)
50787	heparan sulfate 6-O-sulfotransferase 3	Hs6st3	Mus musculus (house mouse)
50786	heparan sulfate 6-O-sulfotransferase 2	Hs6st2	Mus musculus (house mouse)	Paganini-Miozzo syndrome
50785	heparan sulfate 6-O-sulfotransferase 1	Hs6st1	Mus musculus (house mouse)	hypogonadotropic hypogonadism 15 with or without anosmia
50784	phospholipid phosphatase 2	Plpp2	Mus musculus (house mouse)
50781	dickkopf WNT signaling pathway inhibitor 3	Dkk3	Mus musculus (house mouse)
50779	regulator of G-protein signaling 6	Rgs6	Mus musculus (house mouse)
50768	deleted in liver cancer 1	Dlc1	Mus musculus (house mouse)

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