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 ▲
Mitochondrial transcription initiation	DNA-directed RNA polymerase, mitochondrial Dimethyladenosine transferase 2, mitochondrial Transcription factor A, mitochondrial	O00411 Q00059 Q9H5Q4	NS5ATP5 POLRMT TCF6 TCF6L2 TFAM TFB2M
NTF3 activates NTRK2 (TRKB) signaling	BDNF/NT-3 growth factors receptor Neurotrophin-3	P20783 Q16620	NTF3 NTRK2 TRKB
Activated NTRK3 signals through PLCG1	1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase gamma-1 NT-3 growth factor receptor Neurotrophin-3	P19174 P20783 Q16288	NTF3 NTRK3 PLC1 PLCG1 TRKC
NTF3 activates NTRK3 signaling	NT-3 growth factor receptor Neurotrophin-3	P20783 Q16288	NTF3 NTRK3 TRKC
NTF4 activates NTRK2 (TRKB) signaling	BDNF/NT-3 growth factors receptor Neurotrophin-4	P34130 Q16620	NTF4 NTF5 NTRK2 TRKB
Defective SLC22A12 causes renal hypouricemia 1 (RHUC1)	Solute carrier family 22 member 12	Q96S37	OATL4 SLC22A12 URAT1
Defective SLCO2A1 causes primary, autosomal recessive hypertrophic osteoarthropathy 2 (PHOAR2)	Solute carrier organic anion transporter family member 2A1	Q92959	OATP2A1 SLC21A2 SLCO2A1
Defective SLC22A5 causes systemic primary carnitine deficiency (CDSP)	Organic cation/carnitine transporter 2	O76082	OCTN2 SLC22A5
Proton/oligopeptide cotransporters	Solute carrier family 15 member 1 Solute carrier family 15 member 2 Solute carrier family 15 member 3 Solute carrier family 15 member 4	P46059 Q16348 Q8IY34 Q8N697	OCTP PEPT1 PEPT2 PHT1 PHT2 PTR3 PTR4 SLC15A1 SLC15A2 SLC15A3 SLC15A4
Defective OPLAH causes OPLAHD	5-oxoprolinase	O14841	OPLAH
Platelet homeostasis	P2X purinoceptor 1 P2X purinoceptor 2 P2X purinoceptor 3 P2X purinoceptor 4 P2X purinoceptor 5 P2X purinoceptor 6 P2X purinoceptor 7 Platelet-activating factor acetylhydrolase 2, cytoplasmic	O15547 P51575 P56373 Q93086 Q99487 Q99571 Q99572 Q9UBL9	P2RX1 P2RX2 P2RX3 P2RX4 P2RX5 P2RX6 P2RX7 P2RXL1 P2X1 P2X2 P2X5 P2X5FL P2X6 PAFAH2
Loss of function of TP53 in cancer due to loss of tetramerization ability	Cellular tumor antigen p53	P04637	P53 TP53
XAV939 stabilizes AXIN	Poly [ADP-ribose] polymerase tankyrase-1 Poly [ADP-ribose] polymerase tankyrase-2	O95271 Q9H2K2	PARP5A PARP5B PARPL TANK2 TIN1 TINF1 TNKL TNKS TNKS1 TNKS2
Proton-coupled neutral amino acid transporters	Proton-coupled amino acid transporter 1 Proton-coupled amino acid transporter 2	Q495M3 Q7Z2H8	PAT1 PAT2 SLC36A1 SLC36A2 TRAMD1
PDGFR mutants bind TKIs	Platelet-derived growth factor receptor alpha	P16234	PDGFR2 PDGFRA RHEPDGFRA
Sunitinib-resistant PDGFR mutants	Platelet-derived growth factor receptor alpha	P16234	PDGFR2 PDGFRA RHEPDGFRA
Sorafenib-resistant PDGFR mutants	Platelet-derived growth factor receptor alpha	P16234	PDGFR2 PDGFRA RHEPDGFRA
Imatinib-resistant PDGFR mutants	Platelet-derived growth factor receptor alpha	P16234	PDGFR2 PDGFRA RHEPDGFRA
Regorafenib-resistant PDGFR mutants	Platelet-derived growth factor receptor alpha	P16234	PDGFR2 PDGFRA RHEPDGFRA
Defective SLC26A4 causes Pendred syndrome (PDS)	Pendrin	O43511	PDS SLC26A4
Defective PGM1 causes CDG1t	Phosphoglucomutase-1	P36871	PGM1
PI and PC transport between ER and Golgi membranes	Phosphatidylinositol transfer protein beta isoform	P48739	PITPNB
PKA-mediated phosphorylation of CREB	cAMP-dependent protein kinase catalytic subunit PRKX cAMP-dependent protein kinase catalytic subunit alpha cAMP-dependent protein kinase catalytic subunit beta cAMP-dependent protein kinase catalytic subunit gamma	P17612 P22612 P22694 P51817	PKACA PKX1 PRKACA PRKACB PRKACG PRKX
Disinhibition of SNARE formation	Protein kinase C alpha type Protein kinase C beta type Protein kinase C gamma type Syntaxin-4 Syntaxin-binding protein 3	O00186 P05129 P05771 P17252 Q12846	PKCA PKCB PKCG PRKACA PRKCA PRKCB PRKCB1 PRKCG STX4 STX4A STXBP3
Response to elevated platelet cytosolic Ca2+	Protein kinase C alpha type Protein kinase C beta type Protein kinase C gamma type	P05129 P05771 P17252	PKCA PKCB PKCG PRKACA PRKCA PRKCB PRKCB1 PRKCG

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