Homo sapiens (human)

Summary
Taxonomy ID
9606
PubChem Taxonomy
9606
Displaying entries 1901 - 1925 of 2090 in total
Pathway Name Protein Name UniProt ID ▲ Gene Symbol GlyTouCan ID
Classical Kir channels
  • IRK1
  • IRK2
  • IRK3
  • IRK4
  • KCNJ12
  • KCNJ14
  • KCNJ2
  • KCNJ4
  • KCNJN1
Synthesis of PIPs in the nucleus
  • C14orf9
  • PI5P4KA
  • PIP4K2A
  • PIP4K2B
  • PIP4K2C
  • PIP4P1
  • PIP5K2
  • PIP5K2A
  • PIP5K2B
  • PIP5K2C
  • TMEM55B
POU5F1 (OCT4), SOX2, NANOG repress genes related to differentiation
  • NANOG
  • OCT3
  • OCT4
  • OTF3
  • POU5F1
  • SOX2
Defective GCLC causes HAGGSD
  • GCLC
  • GCLM
  • GLCL
  • GLCLC
  • GLCLR
Synthesis of PS
  • KIAA0024
  • PSS2
  • PSSA
  • PTDSS1
  • PTDSS2
PI and PC transport between ER and Golgi membranes
  • PITPNB
Hydroxycarboxylic acid-binding receptors
  • GPR104
  • GPR109A
  • GPR109B
  • GPR81
  • HCA1
  • HCA2
  • HCA3
  • HCAR1
  • HCAR2
  • HCAR3
  • HM74A
  • HM74B
  • NIACR1
  • NIACR2
RPIA deficiency: failed conversion of R5P to RU5P
  • RPI
  • RPIA
RPIA deficiency: failed conversion of RU5P to R5P
  • RPI
  • RPIA
Transport to the Golgi and subsequent modification
  • ERGIC53
  • F5F8D
  • LMAN1
  • MCFD2
  • SDNSF
Defective SLC11A2 causes hypochromic microcytic anemia, with iron overload 1 (AHMIO1)
  • DCT1
  • DMT1
  • NRAMP2
  • SLC11A2
Hypusinylation
  • DHPS
  • DOHH
  • DS
  • EIF5A
  • EIF5A2
  • HLRC1
Choline catabolism
  • ALDH7A1
  • ATQ1
  • BHMT
  • CD92
  • CDW92
  • CHDH
  • CTL1
  • DMGDH
  • DMGDHL1
  • SARDH
  • SLC44A1
Noncanonical activation of NOTCH3
  • AD3
  • AD4
  • APH1A
  • APH1B
  • KIAA0253
  • NCSTN
  • NOTCH3
  • NSEP1
  • PEN2
  • PS1
  • PS2
  • PSEN1
  • PSEN2
  • PSENEN
  • PSF
  • PSFL
  • PSNL1
  • PSNL2
  • STM2
  • YB1
  • YBX1
Maturation of nucleoprotein
  • ADPRTL1
  • ARTD15
  • BAL
  • BAL1
  • BAL2
  • C15orf30
  • GSK3A
  • GSK3B
  • KIAA0177
  • KIAA1268
  • N
  • PARP10
  • PARP14
  • PARP16
  • PARP4
  • PARP6
  • PARP8
  • PARP9
  • PARPL
  • SMT3C
  • SMT3H3
  • SUMO1
  • UBC9
  • UBCE9
  • UBE2I
  • UBL1
Defective SLC26A2 causes chondrodysplasias
  • DTD
  • DTDST
  • SLC26A2
Chromatin modifying enzymes
  • BAF190A
  • BRG1
  • BRWD1
  • C21orf107
  • H3C1
  • H3C10
  • H3C11
  • H3C12
  • H3C13
  • H3C14
  • H3C15
  • H3C2
  • H3C3
  • H3C4
  • H3C6
  • H3C7
  • H3C8
  • H3F2
  • H3FA
  • H3FB
  • H3FC HIST1H3C
  • H3FD
  • H3FF
  • H3FH
  • H3FI
  • H3FJ
  • H3FK
  • H3FL
  • H3FM
  • HIST1H3A
  • HIST1H3B
  • HIST1H3D
  • HIST1H3E
  • HIST1H3F
  • HIST1H3G
  • HIST1H3H
  • HIST1H3I
  • HIST1H3J
  • HIST2H3A
  • HIST2H3C
  • HIST2H3D
  • KIAA0994
  • PAD1
  • PAD2
  • PAD3
  • PAD4
  • PAD6
  • PADI1
  • PADI2
  • PADI3
  • PADI4
  • PADI5
  • PADI6
  • PDI1
  • PDI2
  • PDI3
  • PDI5
  • SMARCA4
  • SNF2B
  • SNF2L4
  • WDR9
Defective GALK1 causes GALCT2
  • GALK
  • GALK1
Defective TPMT causes TPMT deficiency
  • TPMT
Impaired BRCA2 translocation to the nucleus
  • BRCA2
  • C7orf76
  • DSS1
  • FACD
  • FANCD1
  • SEM1
  • SHFDG1
  • SHFM1
Impaired BRCA2 binding to SEM1 (DSS1)
  • BRCA2
  • C7orf76
  • DSS1
  • FACD
  • FANCD1
  • SEM1
  • SHFDG1
  • SHFM1
TRAF6 mediated IRF7 activation in TLR7/8 or 9 signaling
  • BLU
  • CROC1
  • IRAK
  • IRAK1
  • IRAK4
  • IRF7
  • MYD88
  • RNF85
  • TLR7
  • TLR9
  • TRAF6
  • UBE2N
  • UBE2V
  • UBE2V1
  • UEV1
Degradation of GABA
  • ABAT
  • ALDH5A1
  • GABAT
  • SSADH
MPS IIIA - Sanfilippo syndrome A
  • HSS
  • SGSH
CREB1 phosphorylation through NMDA receptor-mediated activation of RAS signaling
  • ISPK1
  • MAPKAPK1A
  • MAPKAPK1B
  • MAPKAPK1C
  • RPS6KA1
  • RPS6KA2
  • RPS6KA3
  • RPS6KA6
  • RSK1
  • RSK2
  • RSK3
  • RSK4

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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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