GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

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

Displaying entries **2026 - 2050** of **2090** in total

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Pathway Name	Protein Name	UniProt ID ▲	Gene Symbol
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
Defective SLC34A3 causes Hereditary hypophosphatemic rickets with hypercalciuria (HHRH)	Sodium-dependent phosphate transport protein 2C	Q8N130	NPT2C NPTIIC SLC34A3
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
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
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
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
Defective SLC17A8 causes autosomal dominant deafness 25 (DFNA25)	Vesicular glutamate transporter 3	Q8NDX2	SLC17A8 VGLUT3
Defective SLC24A4 causes hypomineralized amelogenesis imperfecta (AI)	Sodium/potassium/calcium exchanger 4	Q8NFF2	NCKX4 SLC24A4
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
NEIL3-mediated resolution of ICLs	Endonuclease 8-like 3	Q8TAT5	NEIL3
Defective Base Excision Repair Associated with NEIL3	Endonuclease 8-like 3	Q8TAT5	NEIL3
Eicosanoid ligand-binding receptors	Oxoeicosanoid receptor 1	Q8TDS5	GPR170 OXER1 TG1019
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
Defective SLC9A6 causes X-linked, syndromic mental retardation,, Christianson type (MRXSCH)	Sodium/hydrogen exchanger 6	Q92581	KIAA0267 NHE6 SLC9A6
Defective ABCC2 causes DJS	ATP-binding cassette sub-family C member 2	Q92887	ABCC2 CMOAT CMOAT1 CMRP MRP2
Defective SLC5A5 causes thyroid dyshormonogenesis 1 (TDH1)	Sodium/iodide cotransporter	Q92911	NIS SLC5A5
Defective SLCO2A1 causes primary, autosomal recessive hypertrophic osteoarthropathy 2 (PHOAR2)	Solute carrier organic anion transporter family member 2A1	Q92959	OATP2A1 SLC21A2 SLCO2A1
Regulation of MITF-M dependent genes involved in metabolism	NAD-dependent protein deacetylase sirtuin-1 Peroxisome proliferator-activated receptor gamma coactivator 1-alpha	Q96EB6 Q9UBK2	LEM6 PGC1 PGC1A PPARGC1 PPARGC1A SIR2L1 SIRT1
Defective MMAB causes MMA, cblB type	Corrinoid adenosyltransferase MMAB	Q96EY8	MMAB
Defective ALG14 causes ALG14-CMS	UDP-N-acetylglucosamine transferase subunit ALG13 UDP-N-acetylglucosamine transferase subunit ALG14	Q96F25 Q9NP73	ALG13 ALG14 CXorf45 GLT28D1
Defective SLC6A18 may confer susceptibility to iminoglycinuria and/or hyperglycinuria	Inactive sodium-dependent neutral amino acid transporter B(0)AT3	Q96N87	B0AT3 SLC6A18 XTRP2
Defective SLC6A18 may confer susceptibility to iminoglycinuria and/or hyperglycinuria	Inactive sodium-dependent neutral amino acid transporter B(0)AT3	Q96N87	B0AT3 SLC6A18 XTRP2
Defective SLC22A12 causes renal hypouricemia 1 (RHUC1)	Solute carrier family 22 member 12	Q96S37	OATL4 SLC22A12 URAT1
TWIK-related alkaline pH activated K+ channel (TALK)	Potassium channel subfamily K member 16 Potassium channel subfamily K member 17	Q96T54 Q96T55	KCNK16 KCNK17 TALK1 TALK2 TASK4
Defective MTR causes HMAG	Methionine synthase reductase Methionine synthase	Q99707 Q9UBK8	MTR MTRR

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