Homo sapiens (human)

Summary
Taxonomy ID
9606
PubChem Taxonomy
9606
Displaying entries 7651 - 7675 of 9988 in total
Gene ID Gene Name ▲ Gene Symbol Disease Ontology
5033 prolyl 4-hydroxylase subunit alpha 1
  • P4HA1
8974 prolyl 4-hydroxylase subunit alpha 2
  • P4HA2
283208 prolyl 4-hydroxylase subunit alpha 3
  • P4HA3
5034 prolyl 4-hydroxylase subunit beta
  • P4HB
54681 prolyl 4-hydroxylase, transmembrane
  • P4HTM
5547 prolylcarboxypeptidase
  • PRCP
8842 prominin 1
  • PROM1
150696 prominin 2
  • PROM2
5443 proopiomelanocortin
  • POMC
5095 propionyl-CoA carboxylase subunit alpha
  • PCCA
5096 propionyl-CoA carboxylase subunit beta
  • PCCB
5122 proprotein convertase subtilisin/kexin type 1
  • PCSK1
27344 proprotein convertase subtilisin/kexin type 1 inhibitor
  • PCSK1N
5126 proprotein convertase subtilisin/kexin type 2
  • PCSK2
54760 proprotein convertase subtilisin/kexin type 4
  • PCSK4
5125 proprotein convertase subtilisin/kexin type 5
  • PCSK5
5046 proprotein convertase subtilisin/kexin type 6
  • PCSK6
9159 proprotein convertase subtilisin/kexin type 7
  • PCSK7
255738 proprotein convertase subtilisin/kexin type 9
  • PCSK9
5660 prosaposin
  • PSAP
  • saposin-A
  • saposin-B
  • saposin-C
  • saposin-D
  • variant Gaucher disease and variant metachromatic leukodystrophy
768239 prosaposin like 1
  • PSAPL1
5729 prostaglandin D2 receptor
  • PTGDR
11251 prostaglandin D2 receptor 2
  • PTGDR2
5730 prostaglandin D2 synthase
  • PTGDS
  • L-PGDS
  • PGDS
  • lipocalin-type prostaglandin D synthase
5731 prostaglandin E receptor 1
  • PTGER1

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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: December 9, 2024