Homo sapiens (human)

Summary
Taxonomy ID
9606
PubChem Taxonomy
9606
Displaying entries 101 - 125 of 2090 in total
Pathway Name Protein Name UniProt ID Gene Symbol ▼ GlyTouCan ID
Defective MMAA causes MMA, cblA type
  • MMAA
  • MMUT
  • MUT
Defective MUT causes MMAM
  • MMAA
  • MMUT
  • MUT
Synthesis of IPs in the ER lumen
  • MINPP1
  • MIPP
MGMT-mediated DNA damage reversal
  • MGMT
Defective MGAT2 causes CDG-2a
  • MGAT2
Defective SLC7A7 causes lysinuric protein intolerance (LPI)
  • MDU1
  • SLC3A2
  • SLC7A7
Propionyl-CoA catabolism
  • MCEE
  • MMAA
  • MMUT
  • MUT
  • PCCA
  • PCCB
Defective MAOA causes BRUNS
  • MAOA
Biogenic amines are oxidatively deaminated to aldehydes by MAOA and MAOB
  • MAOA
  • MAOB
Defective MAN1B1 causes MRT15
  • MAN1B1
Progressive trimming of alpha-1,2-linked mannose residues from Man9/8/7GlcNAc2 to produce Man5GlcNAc2
  • MAN1A1
  • MAN1A2
  • MAN1A3
  • MAN1B
  • MAN1C
  • MAN1C1
Translesion synthesis by REV1
  • MAD2B
  • MAD2L2
  • PCNA
  • POLZ
  • REPA1
  • REPA2
  • REPA3
  • REV1
  • REV1L
  • REV3
  • REV3L
  • REV7
  • RFC1
  • RFC140
  • RFC2
  • RFC3
  • RFC4
  • RFC5
  • RPA1
  • RPA14
  • RPA2
  • RPA3
  • RPA32
  • RPA34
  • RPA70
  • RPS27A
  • UBA52
  • UBA80
  • UBB
  • UBC
  • UBCEP1
  • UBCEP2
Translesion synthesis by POLI
  • MAD2B
  • MAD2L2
  • PCNA
  • POLI
  • POLZ
  • RAD30B
  • REPA1
  • REPA2
  • REPA3
  • REV1
  • REV1L
  • REV3
  • REV3L
  • REV7
  • RFC1
  • RFC140
  • RFC2
  • RFC3
  • RFC4
  • RFC5
  • RPA1
  • RPA14
  • RPA2
  • RPA3
  • RPA32
  • RPA34
  • RPA70
  • RPS27A
  • UBA52
  • UBA80
  • UBB
  • UBC
  • UBCEP1
  • UBCEP2
Maturation of protein M
  • M
Maturation of protein M
  • M
LXRs regulate gene expression linked to gluconeogenesis
  • LXRA
  • NR1H3
  • NR2B1
  • NR2B2
  • NRIP1
  • PCK1
  • PEPCK1
  • RXRA
  • RXRB
LXRs regulate gene expression linked to triglyceride lipolysis in adipose
  • LXRA
  • LXRB
  • NER
  • NR1H2
  • NR1H3
  • NR2B1
  • NR2B2
  • PERI
  • PLIN
  • PLIN1
  • RXRA
  • RXRB
  • UNR
Defective SLCO1B3 causes hyperbilirubinemia, Rotor type (HBLRR)
  • LST2
  • OATP1B3
  • OATP8
  • SLC21A8
  • SLCO1B3
Defective SLCO1B1 causes hyperbilirubinemia, Rotor type (HBLRR)
  • LST1
  • OATP1B1
  • OATP2
  • OATPC
  • SLC21A6
  • SLCO1B1
Events associated with phagocytolytic activity of PMN cells
  • LPO
  • MPO
  • SAPX
Resolution of AP sites via the single-nucleotide replacement pathway
  • LIG3
  • POLB
  • XRCC1
APEX1-Independent Resolution of AP Sites via the Single Nucleotide Replacement Pathway
  • LIG3
  • MMH
  • MUTM
  • NEIL1
  • NEIL2
  • OGG1
  • OGH1
  • PNKP
  • POLB
  • XRCC1
Regulation of MITF-M dependent genes involved in metabolism
  • LEM6
  • PGC1
  • PGC1A
  • PPARGC1
  • PPARGC1A
  • SIR2L1
  • SIRT1
Intestinal saccharidase deficiencies
  • LCT
  • LPH
  • SI
Inositol transporters
  • KST1
  • SLC2A13
  • SLC5A11
  • SLC5A3
  • SLGTX
  • SMIT2

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: August 19, 2024