Homo sapiens (human)

Summary
Taxonomy ID
9606
PubChem Taxonomy
9606
Displaying entries 51 - 75 of 2090 in total
Pathway Name Protein Name ▼ UniProt ID Gene Symbol GlyTouCan ID
Defective SLC24A1 causes congenital stationary night blindness 1D (CSNB1D)
  • KIAA0702
  • NCKX1
  • SLC24A1
Defective SLC5A5 causes thyroid dyshormonogenesis 1 (TDH1)
  • NIS
  • SLC5A5
Defective SLC9A9 causes autism 16 (AUTS16)
  • NHE9
  • SLC9A9
Defective SLC9A6 causes X-linked, syndromic mental retardation,, Christianson type (MRXSCH)
  • KIAA0267
  • NHE6
  • SLC9A6
Sodium/Proton exchangers
  • APNH1
  • KIAA0267
  • KIAA0939
  • NHE1
  • NHE2
  • NHE3
  • NHE4
  • NHE5
  • NHE6
  • NHE7
  • NHE8
  • NHE9
  • SLC9A1
  • SLC9A2
  • SLC9A3
  • SLC9A4
  • SLC9A5
  • SLC9A6
  • SLC9A7
  • SLC9A8
  • SLC9A9
Defective SLC5A2 causes renal glucosuria (GLYS1)
  • SGLT2
  • SLC5A2
Defective SLC5A1 causes congenital glucose/galactose malabsorption (GGM)
  • NAGT
  • SGLT1
  • SLC5A1
Clearance of seratonin
  • HTT
  • SERT
  • SLC6A4
Defective SLC20A2 causes idiopathic basal ganglia calcification 1 (IBGC1)
  • GLVR2
  • PIT2
  • SLC20A2
Sodium-coupled phosphate cotransporters
  • GLVR1
  • GLVR2
  • PIT1
  • PIT2
  • SLC20A1
  • SLC20A2
Defective SLC34A3 causes Hereditary hypophosphatemic rickets with hypercalciuria (HHRH)
  • NPT2C
  • NPTIIC
  • SLC34A3
Defective SLC34A2 causes PALM
  • SLC34A2
Defective SLC34A2 causes pulmonary alveolar microlithiasis (PALM)
  • SLC34A2
Defective SLC34A1 causes hypophosphatemic nephrolithiasis/osteoporosis 1 (NPHLOP1)
  • NPT2
  • SLC17A2
  • SLC34A1
Type II Na+/Pi cotransporters
  • NPT2
  • NPT2C
  • NPTIIC
  • SLC17A2
  • SLC34A1
  • SLC34A2
  • SLC34A3
Defective SLC6A2 causes orthostatic intolerance (OI)
  • NAT1
  • NET1
  • SLC6A2
  • SLC6A5
Defective SLC6A19 causes Hartnup disorder (HND)
  • B0AT1
  • SLC6A19
Defective SLC6A19 causes Hartnup disorder (HND)
  • B0AT1
  • SLC6A19
Defective SLC6A3 causes Parkinsonism-dystonia infantile (PKDYS)
  • DAT1
  • SLC6A3
Defective SLC6A3 causes Parkinsonism-dystonia infantile (PKDYS)
  • DAT1
  • SLC6A3
Variant SLC6A20 contributes towards hyperglycinuria (HG) and iminoglycinuria (IG)
  • SIT1
  • SLC6A20
  • XT3
  • XTRP3
Variant SLC6A20 contributes towards hyperglycinuria (HG) and iminoglycinuria (IG)
  • SIT1
  • SLC6A20
  • XT3
  • XTRP3
Variant SLC6A14 may confer susceptibility towards obesity
  • SLC6A14
Defective SLC6A5 causes hyperekplexia 3 (HKPX3)
  • GLYT2
  • NET1
  • SLC6A5
Reuptake of GABA
  • BGT1
  • GABATR
  • GABT1
  • GABT3
  • GAT1
  • GAT2
  • GAT3
  • SLC6A1
  • SLC6A11
  • SLC6A12
  • SLC6A13

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