GlyCosmos Portal

GlyCosmos Pathways

Integrated of pathway data, containing glycoproteins and glycans obtained from Reactome and the Metabolism of carbohydrates in Escherichia coli O-antigens obtained from ECODAB. Search by pathway name, species, and protein name.

Source	Last Updated
Reactome	November 12, 2024
ECODAB	April 1, 2019

Displaying entries **2001 - 2025** of **2074** in total

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Pathway Name	Protein Name	UniProt ID ▲	Gene Symbol	Organism	GlyTouCan ID
Defective DHDDS causes RP59	Dehydrodolichyl diphosphate synthase complex subunit DHDDS Dehydrodolichyl diphosphate synthase complex subunit NUS1	Q86SQ9 Q96E22	C6orf68 DHDDS HDS NGBR NUS1	Homo sapiens (human)
Defective ABCA12 causes ARCI4B	Glucosylceramide transporter ABCA12	Q86UK0	ABC12 ABCA12	Homo sapiens (human)
Regulation of NPAS4 mRNA translation	Helicase MOV-10 Neuronal PAS domain-containing protein 4 Protein argonaute-1 Protein argonaute-2 Protein argonaute-3 Protein argonaute-4 Trinucleotide repeat-containing gene 6A protein Trinucleotide repeat-containing gene 6B protein Trinucleotide repeat-containing gene 6C protein	Q8IUM7 Q8NDV7 Q9H9G7 Q9HCE1 Q9HCJ0 Q9HCK5 Q9UKV8 Q9UL18 Q9UPQ9	AGO1 AGO2 AGO3 AGO4 BHLHE79 CAGH26 EIF2C1 EIF2C2 EIF2C3 EIF2C4 KIAA1093 KIAA1460 KIAA1567 KIAA1582 KIAA1631 MOV10 NPAS4 NXF PASD10 TNRC6 TNRC6A TNRC6B TNRC6C	Homo sapiens (human)
Defective SLC9A9 causes autism 16 (AUTS16)	Sodium/hydrogen exchanger 9	Q8IVB4	NHE9 SLC9A9	Homo sapiens (human)
Defective SFTPA2 causes IPF	Pulmonary surfactant-associated protein A2	Q8IWL1	COLEC5 PSAP SFTP1 SFTPA SFTPA2 SFTPA2B	Homo sapiens (human)
Zinc efflux and compartmentalization by the SLC30 family	Probable proton-coupled zinc antiporter SLC30A3 Proton-coupled zinc antiporter SLC30A1 Proton-coupled zinc antiporter SLC30A2 Proton-coupled zinc antiporter SLC30A5 Proton-coupled zinc antiporter SLC30A8	Q8IWU4 Q8TAD4 Q99726 Q9BRI3 Q9Y6M5	SLC30A1 SLC30A2 SLC30A3 SLC30A5 SLC30A8 ZNT1 ZNT2 ZNT3 ZNT5 ZNT8 ZNTL1 ZTL1	Homo sapiens (human)
Interconversion of 2-oxoglutarate and 2-hydroxyglutarate	D-2-hydroxyglutarate dehydrogenase, mitochondrial Hydroxyacid-oxoacid transhydrogenase, mitochondrial L-2-hydroxyglutarate dehydrogenase, mitochondrial	Q8IWW8 Q8N465 Q9H9P8	ADHFE1 C14orf160 D2HGD D2HGDH L2HGDH	Homo sapiens (human)
Defective SLC34A3 causes Hereditary hypophosphatemic rickets with hypercalciuria (HHRH)	Sodium-dependent phosphate transport protein 2C	Q8N130	NPT2C NPTIIC SLC34A3	Homo sapiens (human)
Arachidonate production from DAG	Diacylglycerol lipase-alpha Diacylglycerol lipase-beta Lysophosphatidylserine lipase ABHD12 Monoacylglycerol lipase ABHD6 Monoglyceride lipase	Q8N2K0 Q8NCG7 Q99685 Q9BV23 Q9Y4D2	ABHD12 ABHD6 C11orf11 C20orf22 DAGLA DAGLB KIAA0659 MGLL NSDDR	Homo sapiens (human)
ALKBH3 mediated reversal of alkylation damage	Activating signal cointegrator 1 complex subunit 1 Activating signal cointegrator 1 complex subunit 2 Activating signal cointegrator 1 complex subunit 3 Alpha-ketoglutarate-dependent dioxygenase alkB homolog 3	Q8N3C0 Q8N9N2 Q96Q83 Q9H1I8	ABH3 ALKBH3 ASC1P100 ASCC1 ASCC2 ASCC3 DEPC1 HELIC1 RQT2 RQT3	Homo sapiens (human)
Glycosaminoglycan metabolism	UDP-glucuronic acid decarboxylase 1	Q8NBZ7	UXS1	Homo sapiens (human)
Competing endogenous RNAs (ceRNAs) regulate PTEN translation	Helicase MOV-10 Protein argonaute-1 Protein argonaute-2 Protein argonaute-3 Protein argonaute-4 Trinucleotide repeat-containing gene 6A protein Trinucleotide repeat-containing gene 6B protein Trinucleotide repeat-containing gene 6C protein	Q8NDV7 Q9H9G7 Q9HCE1 Q9HCJ0 Q9HCK5 Q9UKV8 Q9UL18 Q9UPQ9	AGO1 AGO2 AGO3 AGO4 CAGH26 EIF2C1 EIF2C2 EIF2C3 EIF2C4 KIAA1093 KIAA1460 KIAA1567 KIAA1582 KIAA1631 MOV10 TNRC6 TNRC6A TNRC6B TNRC6C	Homo sapiens (human)
Post-transcriptional silencing by small RNAs	Protein argonaute-1 Protein argonaute-2 Protein argonaute-3 Protein argonaute-4 Trinucleotide repeat-containing gene 6A protein Trinucleotide repeat-containing gene 6B protein Trinucleotide repeat-containing gene 6C protein	Q8NDV7 Q9H9G7 Q9HCJ0 Q9HCK5 Q9UKV8 Q9UL18 Q9UPQ9	AGO1 AGO2 AGO3 AGO4 CAGH26 EIF2C1 EIF2C2 EIF2C3 EIF2C4 KIAA1093 KIAA1460 KIAA1567 KIAA1582 TNRC6 TNRC6A TNRC6B TNRC6C	Homo sapiens (human)
Defective SLC17A8 causes autosomal dominant deafness 25 (DFNA25)	Vesicular glutamate transporter 3	Q8NDX2	SLC17A8 VGLUT3	Homo sapiens (human)
Defective SLC24A4 causes hypomineralized amelogenesis imperfecta (AI)	Sodium/potassium/calcium exchanger 4	Q8NFF2	NCKX4 SLC24A4	Homo sapiens (human)
Synthesis of IPs in the nucleus	Inositol hexakisphosphate kinase 1 Inositol hexakisphosphate kinase 2 Inositol polyphosphate multikinase Inositol-pentakisphosphate 2-kinase	Q8NFU5 Q92551 Q9H8X2 Q9UHH9	C9orf12 IHPK1 IHPK2 IMPK IP6K1 IP6K2 IPMK IPPK KIAA0263	Homo sapiens (human)
NEIL3-mediated resolution of ICLs	Endonuclease 8-like 3	Q8TAT5	NEIL3	Homo sapiens (human)
Defective Base Excision Repair Associated with NEIL3	Endonuclease 8-like 3	Q8TAT5	NEIL3	Homo sapiens (human)
Eicosanoid ligand-binding receptors	Oxoeicosanoid receptor 1	Q8TDS5	GPR170 OXER1 TG1019	Homo sapiens (human)
Interleukin-36 pathway	Interleukin-1 family member 10 Interleukin-1 receptor-like 2 Interleukin-36 alpha Interleukin-36 beta Interleukin-36 gamma Interleukin-36 receptor antagonist protein	Q8WWZ1 Q9HB29 Q9NZH7 Q9NZH8 Q9UBH0 Q9UHA7	FIL1D FIL1E FIL1T IL1E IL1F10 IL1F5 IL1F6 IL1F8 IL1F9 IL1H1 IL1H2 IL1HY1 IL1HY2 IL1L1 IL1RL2 IL1RP2 IL1RP3 IL1RRP2 IL36A IL36B IL36G IL36RN IL38	Homo sapiens (human)
Defective SLC9A6 causes X-linked, syndromic mental retardation,, Christianson type (MRXSCH)	Sodium/hydrogen exchanger 6	Q92581	KIAA0267 NHE6 SLC9A6	Homo sapiens (human)
Defective ALG3 causes CDG-1d	Dol-P-Man	Q92685	ALG3 NOT NOT56L	Homo sapiens (human)	G59406KS
Defective ABCC2 causes DJS	ATP-binding cassette sub-family C member 2	Q92887	ABCC2 CMOAT CMOAT1 CMRP MRP2	Homo sapiens (human)
Defective SLC5A5 causes thyroid dyshormonogenesis 1 (TDH1)	Sodium/iodide cotransporter	Q92911	NIS SLC5A5	Homo sapiens (human)
Defective SLCO2A1 causes primary, autosomal recessive hypertrophic osteoarthropathy 2 (PHOAR2)	Solute carrier organic anion transporter family member 2A1	Q92959	OATP2A1 SLC21A2 SLCO2A1	Homo sapiens (human)

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