Homo sapiens (human)

Summary
Taxonomy ID
9606
PubChem Taxonomy
9606
Displaying entries 1976 - 2000 of 2090 in total
Pathway Name Protein Name UniProt ID ▲ Gene Symbol GlyTouCan ID
Defective ABCC8 can cause hypo- and hyper-glycemias
  • ABCC8
  • HRINS
  • KCNJ11
  • SUR
  • SUR1
Defective MGAT2 causes CDG-2a
  • MGAT2
Acetylcholine inhibits contraction of outer hair cells
  • CHRNA10
  • CHRNA9
  • KCNMA
  • KCNMA1
  • KCNMB1
  • KCNN2
  • NACHRA10
  • NACHRA9
  • SLO
MPS IX - Natowicz syndrome
  • HYAL1
  • LUCA1
Inhibition of the proteolytic activity of APC/C required for the onset of anaphase by mitotic spindle checkpoint components
  • CDC20
  • MAD2
  • MAD2L1
Defective RIPK1-mediated regulated necrosis
  • CASP8
  • FADD
  • MCH5
  • MORT1
  • RIP
  • RIP1
  • RIPK1
  • TRADD
  • TRAF2
  • TRAP3
Coenzyme A biosynthesis
  • C20orf48
  • COAB
  • COAC
  • COASY
  • DCAKD
  • PANK
  • PANK1
  • PANK2
  • PANK3
  • PPCDC
  • PPCS
Signalling to ERK5
  • BMK1
  • ERK5
  • MAP2K5
  • MAPK7
  • MEK5
  • MKK5
  • PRKM7
  • PRKMK5
Sodium-coupled sulphate, di- and tri-carboxylate transporters
  • NACT
  • NADC1
  • NADC3
  • NAS1
  • NASI1
  • SDCT1
  • SDCT2
  • SLC13A1
  • SLC13A2
  • SLC13A3
  • SLC13A4
  • SLC13A5
  • SUT1
Leukotriene receptors
  • BLT
  • BLT1
  • BLT2R
  • BLTR
  • BLTR2
  • CMKRL1
  • CYSLT1
  • CYSLT2
  • CYSLT2R
  • CYSLTR1
  • CYSLTR2
  • GPR16
  • GPR17
  • LTB4R
  • LTB4R2
  • P2RY7
Transport of bile salts and organic acids, metal ions and amine compounds
  • C6orf29
  • CD92
  • CDW92
  • CHT1
  • CTL1
  • CTL2
  • CTL3
  • CTL4
  • CTL5
  • HUT11
  • HUT2
  • JK
  • MATE1
  • MATE2
  • NG22
  • RACH1
  • SLC10A6
  • SLC14A1
  • SLC14A2
  • SLC44A1
  • SLC44A2
  • SLC44A3
  • SLC44A4
  • SLC44A5
  • SLC47A1
  • SLC47A2
  • SLC5A7
  • SOAT
  • TPPT1
  • UT1
  • UT2
  • UTE
Zinc influx into cells by the SLC39 gene family
  • BIGM103
  • HKE4
  • IRT1
  • KIAA0062
  • KIAA1265
  • LIV1
  • RING5
  • SLC39A1
  • SLC39A10
  • SLC39A14
  • SLC39A2
  • SLC39A3
  • SLC39A4
  • SLC39A5
  • SLC39A6
  • SLC39A7
  • SLC39A8
  • ZIP1
  • ZIP10
  • ZIP14
  • ZIP2
  • ZIP3
  • ZIP4
  • ZIP5
  • ZIP6
  • ZIP8
  • ZIRTL
Loss of MECP2 binding ability to 5mC-DNA
  • HDAC1
  • RPD3L1
  • SIN3A
Defective SLC12A1 causes Bartter syndrome 1 (BS1)
  • NKCC2
  • SLC12A1
Defective MOGS causes CDG-2b
  • GCS1
  • MOGS
RUNX3 regulates RUNX1-mediated transcription
  • AML2
  • CBFA3
  • CBFB
  • PEBP2A3
  • RUNX3
Defective POMGNT1 causes MDDGA3, MDDGB3 and MDDGC3
  • DAG1
  • MGAT1.2
  • POMGNT1
Defective POMT1 causes MDDGA1, MDDGB1 and MDDGC1
  • DAG1
  • POMT1
  • POMT2
Defective POMT2 causes MDDGA2, MDDGB2 and MDDGC2
  • DAG1
  • POMT1
  • POMT2
Defective GALE causes EDG
  • GALE
IRF3 mediated activation of type 1 IFN
  • C20orf183
  • DLM1
  • DTX4
  • IRF3
  • KIAA0937
  • NAK
  • NALP4
  • NLRP4
  • PAN2
  • PYPAF4
  • RNF155
  • RNH2
  • TBK1
  • ZBP1
Toll Like Receptor 9 (TLR9) Cascade
  • EEA1
  • PIK3C3
  • PIK3R4
  • RBSN
  • TLR9
  • VPS15
  • VPS34
  • ZFYVE2
  • ZFYVE20
Pyrophosphate hydrolysis
  • IOPPP
  • LHPP
  • PP
  • PPA1
  • PPA2
Cellular response to hypoxia
  • BHLHE73
  • BHLHE78
  • EPAS1
  • FIH1
  • HIF1A
  • HIF1AN
  • HIF2A
  • MOP1
  • MOP2
  • PASD2
  • PASD8
Defective CYP1B1 causes Glaucoma
  • CYP1B1

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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