GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

Genes (1582) Glycans (5831) Glycoproteins (18496) Lectins (298) Pathways (2090)

Displaying entries **51 - 75** of **2090** in total

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Pathway Name	Protein Name	UniProt ID ▼	Gene Symbol
Defective ABCC2 causes DJS	ATP-binding cassette sub-family C member 2	Q92887	ABCC2 CMOAT CMOAT1 CMRP MRP2
Defective SLC9A6 causes X-linked, syndromic mental retardation,, Christianson type (MRXSCH)	Sodium/hydrogen exchanger 6	Q92581	KIAA0267 NHE6 SLC9A6
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
Eicosanoid ligand-binding receptors	Oxoeicosanoid receptor 1	Q8TDS5	GPR170 OXER1 TG1019
NEIL3-mediated resolution of ICLs	Endonuclease 8-like 3	Q8TAT5	NEIL3
Defective Base Excision Repair Associated with NEIL3	Endonuclease 8-like 3	Q8TAT5	NEIL3
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
Defective SLC24A4 causes hypomineralized amelogenesis imperfecta (AI)	Sodium/potassium/calcium exchanger 4	Q8NFF2	NCKX4 SLC24A4
Defective SLC17A8 causes autosomal dominant deafness 25 (DFNA25)	Vesicular glutamate transporter 3	Q8NDX2	SLC17A8 VGLUT3
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
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
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
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
Defective SLC34A3 causes Hereditary hypophosphatemic rickets with hypercalciuria (HHRH)	Sodium-dependent phosphate transport protein 2C	Q8N130	NPT2C NPTIIC SLC34A3
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
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
Defective SFTPA2 causes IPF	Pulmonary surfactant-associated protein A2	Q8IWL1	COLEC5 PSAP SFTP1 SFTPA SFTPA2 SFTPA2B
Defective SLC9A9 causes autism 16 (AUTS16)	Sodium/hydrogen exchanger 9	Q8IVB4	NHE9 SLC9A9
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
Defective ABCA12 causes ARCI4B	Glucosylceramide transporter ABCA12	Q86UK0	ABC12 ABCA12
Defective DHDDS causes RP59	Dehydrodolichyl diphosphate synthase complex subunit DHDDS Dehydrodolichyl diphosphate synthase complex subunit NUS1	Q86SQ9 Q96E22	C6orf68 DHDDS HDS NGBR NUS1
Essential pentosuria	L-xylulose reductase	Q7Z4W1	DCXR SDR20C1
TWIK-related spinal cord K+ channel (TRESK)	Potassium channel subfamily K member 18	Q7Z418	KCNK18 TRESK TRIK
FASTK family proteins regulate processing and stability of mitochondrial RNAs	FAST kinase domain-containing protein 2, mitochondrial FAST kinase domain-containing protein 4 FAST kinase domain-containing protein 5, mitochondrial	Q7L8L6 Q969Z0 Q9NYY8	CPR2 FASTKD2 FASTKD4 FASTKD5 KIAA0948 KIAA0971 KIAA1792 TBRG4
Glycerophospholipid catabolism	Glycerophosphocholine cholinephosphodiesterase ENPP6 Glycerophosphodiester phosphodiesterase 1 Glycerophosphodiester phosphodiesterase domain-containing protein 5 Lysophospholipase D GDPD1 Lysophospholipase D GDPD3 Patatin-like phospholipase domain-containing protein 6 Patatin-like phospholipase domain-containing protein 7	Q6UWR7 Q6ZV29 Q7L5L3 Q8IY17 Q8N9F7 Q8WTR4 Q9NZC3	C9orf111 ENPP6 GDE1 GDE2 GDE4 GDE7 GDPD1 GDPD3 GDPD5 MIR16 NTE PNPLA6 PNPLA7

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