GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

Genes (9988) Glycans (5831) Glycoproteins (15733) Lectins (298) Pathways (2074)

Displaying entries **51 - 75** of **2074** in total

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Pathway Name	Protein Name	UniProt ID	Gene Symbol ▼
Defective OPLAH causes OPLAHD	5-oxoprolinase	O14841	OPLAH
Proton/oligopeptide cotransporters	Solute carrier family 15 member 1 Solute carrier family 15 member 3 Solute carrier family 15 member 4	P46059 Q8IY34 Q8N697	OCTP PEPT1 PHT1 PHT2 PTR3 PTR4 SLC15A1 SLC15A3 SLC15A4
Defective SLC22A5 causes systemic primary carnitine deficiency (CDSP)	Organic cation/carnitine transporter 2	O76082	OCTN2 SLC22A5
Defective SLCO2A1 causes primary, autosomal recessive hypertrophic osteoarthropathy 2 (PHOAR2)	Solute carrier organic anion transporter family member 2A1	Q92959	OATP2A1 SLC21A2 SLCO2A1
Defective SLC22A12 causes renal hypouricemia 1 (RHUC1)	Solute carrier family 22 member 12	Q96S37	OATL4 SLC22A12 URAT1
NTF4 activates NTRK2 (TRKB) signaling	BDNF/NT-3 growth factors receptor Neurotrophin-4	P34130 Q16620	NTF4 NTF5 NTRK2 TRKB
NTF3 activates NTRK3 signaling	NT-3 growth factor receptor Neurotrophin-3	P20783 Q16288	NTF3 NTRK3 TRKC
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 NTRK2 (TRKB) signaling	BDNF/NT-3 growth factors receptor Neurotrophin-3	P20783 Q16620	NTF3 NTRK2 TRKB
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
Defective SLC34A3 causes Hereditary hypophosphatemic rickets with hypercalciuria (HHRH)	Sodium-dependent phosphate transport protein 2C	Q8N130	NPT2C NPTIIC SLC34A3
Defective SLC34A1 causes hypophosphatemic nephrolithiasis/osteoporosis 1 (NPHLOP1)	Sodium-dependent phosphate transport protein 2A	Q06495	NPT2 SLC17A2 SLC34A1
Type II Na+/Pi cotransporters	Sodium-dependent phosphate transport protein 2A Sodium-dependent phosphate transport protein 2B Sodium-dependent phosphate transport protein 2C	O95436 Q06495 Q8N130	NPT2 NPT2C NPTIIC SLC17A2 SLC34A1 SLC34A2 SLC34A3
NOSIP mediated eNOS trafficking	Nitric oxide synthase 3 Nitric oxide synthase-interacting protein	P29474 Q9Y314	NOS3 NOSIP
Late Phase of HIV Life Cycle	Glycylpeptide N-tetradecanoyltransferase 1 Protein Nef	P04601 P30419	NMT NMT1 nef
Organic anion transport	Organic anion transporter 3 Solute carrier family 22 member 11 Solute carrier family 22 member 12 Solute carrier family 22 member 6 Solute carrier family 22 member 7	Q4U2R8 Q8TCC7 Q96S37 Q9NSA0 Q9Y694	NLT OAT1 OAT2 OAT3 OAT4 OATL4 PAHT SLC22A11 SLC22A12 SLC22A6 SLC22A7 SLC22A8 URAT1
Defective SLC12A1 causes Bartter syndrome 1 (BS1)	Solute carrier family 12 member 1	Q13621	NKCC2 SLC12A1
Tachykinin receptors bind tachykinins	Neuromedin-K receptor Protachykinin-1 Substance-K receptor Substance-P receptor Tachykinin-3	P20366 P21452 P25103 P29371 Q9UHF0	NK1R NK2R NK3R NKA NKNA NKNAR NKNB TAC1 TAC1R TAC2 TAC2R TAC3 TAC3R TACR1 TACR2 TACR3
Defective SLC5A5 causes thyroid dyshormonogenesis 1 (TDH1)	Sodium/iodide cotransporter	Q92911	NIS SLC5A5
Defective SLC9A9 causes autism 16 (AUTS16)	Sodium/hydrogen exchanger 9	Q8IVB4	NHE9 SLC9A9
NFG and proNGF binds to p75NTR	Beta-nerve growth factor Sortilin-related VPS10 domain containing receptor 3 Tumor necrosis factor receptor superfamily member 16	P01138 P08138 Q17R88	NGF NGFB NGFR SORCS3 TNFRSF16
Ceramide signalling	Beta-nerve growth factor Sphingomyelin phosphodiesterase 2 Tumor necrosis factor receptor superfamily member 16	O60906 P01138 P08138	NGF NGFB NGFR SMPD2 TNFRSF16
Defective Base Excision Repair Associated with NEIL3	Endonuclease 8-like 3	Q8TAT5	NEIL3
NEIL3-mediated resolution of ICLs	Endonuclease 8-like 3	Q8TAT5	NEIL3
Peptide hormone biosynthesis	Neuroendocrine convertase 1 Pro-opiomelanocortin	P01189 P29120	NEC1 PCSK1 POMC

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