Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
5066
Gene name Gene Name - the full gene name approved by the HGNC.
Peptidylglycine alpha-amidating monooxygenase
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
PAM
Synonyms (NCBI Gene) Gene synonyms aliases
PAL, PAM-1, PHM
Chromosome Chromosome number
5
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
5q21.1
Summary Summary of gene provided in NCBI Entrez Gene.
This gene encodes a multifunctional protein. The encoded preproprotein is proteolytically processed to generate the mature enzyme. This enzyme includes two domains with distinct catalytic activities, a peptidylglycine alpha-hydroxylating monooxygenase (PH
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT047841 hsa-miR-30c-5p CLASH 23622248
MIRT046087 hsa-miR-125b-5p CLASH 23622248
MIRT045767 hsa-miR-125a-5p CLASH 23622248
MIRT440051 hsa-miR-218-5p HITS-CLIP 23212916
MIRT440051 hsa-miR-218-5p HITS-CLIP 23212916
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0001519 Process Peptide amidation IDA 2357221, 12699694
GO:0001666 Process Response to hypoxia IEA
GO:0001676 Process Long-chain fatty acid metabolic process IEA
GO:0004504 Function Peptidylglycine monooxygenase activity IBA 21873635
GO:0004504 Function Peptidylglycine monooxygenase activity IDA 2357221, 12699694
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
170270 8596 ENSG00000145730
Protein
UniProt ID P19021
Protein name Peptidyl-glycine alpha-amidating monooxygenase (PAM) [Includes: Peptidylglycine alpha-hydroxylating monooxygenase (PHM) (EC 1.14.17.3); Peptidyl-alpha-hydroxyglycine alpha-amidating lyase (EC 4.3.2.5) (Peptidylamidoglycolate lyase) (PAL)]
Protein function Bifunctional enzyme that catalyzes amidation of the C-terminus of proteins (PubMed:12699694, PubMed:2357221). Alpha-amidation is present at the C-terminus of many endocrine hormones and neuropeptides and is required for their activity (PubMed:15
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF01082 Cu2_monooxygen 59 175 Copper type II ascorbate-dependent monooxygenase, N-terminal domain Domain
PF03712 Cu2_monoox_C 195 342 Copper type II ascorbate-dependent monooxygenase, C-terminal domain Domain
PF01436 NHL 630 659 NHL repeat Repeat
PF01436 NHL 683 711 NHL repeat Repeat
PF01436 NHL 779 806 NHL repeat Repeat
Sequence
MAGRVPSLLVLLVFPSSCLAFRSPLSVFKRFKETTRPFSNECLGTTRPVVPIDSSDFALD
IRMPGVTPKQSDTYFCMSMRIPVDEEAFVIDFKPRASMDTVHHMLLFGCNMPSSTGSYWF
CDEGTCTDKANILYAWARNAPPTRLPKGVGFRVGGETGSKYFVLQVHYGDISAFR
DNNKD
CSGVSLHLTRLPQPLIAGMYLMMSVDTVIPAGEKVVNSDISCHYKNYPMHVFAYRVHTHH
LGKVVSGYRVRNGQWTLIGRQSPQLPQAFYPVGHPVDVSFGDLLAARCVFTGEGRTEATH
IGGTSSDEMCNLYIMYYMEAKHAVSFMTCTQNVAPDMFRTIP
PEANIPIPVKSDMVMMHE
HHKETEYKDKIPLLQQPKREEEEVLDQGDFYSLLSKLLGEREDVVHVHKYNPTEKAESES
DLVAEIANVVQKKDLGRSDAREGAEHERGNAILVRDRIHKFHRLVSTLRPPESRVFSLQQ
PPPGEGTWEPEHTGDFHMEEALDWPGVYLLPGQVSGVALDPKNNLVIFHRGDHVWDGNSF
DSKFVYQQIGLGPIEEDTILVIDPNNAAVLQSSGKNLFYLPHGLSIDKDGNYWVTDVALH
QVFKLDPNNKEGPVLILGRSMQPGSDQNHFCQPTDVAVDPGTGAIYVSDGYCNSRIVQFS
PSGKFITQWGEESSGSSPLPGQFTVPHSLALVPLLGQLCVADRENGRIQCFKTDTKEFVR
EIKHSSFGRNVFAISYIPGLLFAVNGKPHFGDQEPVQGFVMNFSNGEIIDIFKPVRKHFD
MPHDIVASEDGTVYIGDAHTNTVWKF
TLTEKLEHRSVKKAGIEVQEIKEAEAVVETKMEN
KPTSSELQKMQEKQKLIKEPGSGVPVVLITTLLVIPVVVLLAIAIFIRWKKSRAFGDSEH
KLETSSGRVLGRFRGKGSGGLNLGNFFASRKGYSRKGFDRLSTEGSDQEKEDDGSESEEE
YSAPLPALAPSSS
Sequence length 973
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Diabetes mellitus Diabetes Mellitus, Non-Insulin-Dependent rs587776515, rs61730328, rs606231121, rs606231122, rs79020217, rs77625743, rs78378398, rs606231123, rs1362648752, rs104893649, rs80356624, rs80356616, rs80356625, rs80356611, rs104894237
View all (293 more)
29632382, 30054458, 24464100, 30595370, 30054598
Leukemia Leukemia, Myelocytic, Acute rs121909646, rs121913488, rs587776834, rs752746786, rs869312821, rs767454740, rs1554564297 27903959
Parkinson disease Parkinson Disease rs33939927, rs35801418, rs34805604, rs35870237, rs34995376, rs74315355, rs28940284, rs74315356, rs74315357, rs28940285, rs730880302, rs750664040, rs74315359, rs74315360, rs45539432
View all (84 more)
28892059
Seizure Complex partial seizures, Generalized seizures, Visual seizure, Tonic - clonic seizures, Single Seizure rs587784365, rs28939683, rs74315390, rs28939684, rs74315391, rs267607198, rs74315392, rs118192244, rs118192250, rs121917749, rs121917750, rs121917751, rs121917752, rs267606670, rs267607061
View all (179 more)
19815072
Unknown
Disease term Disease name Evidence References Source
Parkinson Disease Parkinson Disease GWAS
Diabetes Diabetes GWAS
Insomnia Insomnia GWAS
Restless Legs Syndrome Restless Legs Syndrome GWAS
Associations from Text Mining
Disease Name Relationship Type References
Adrenocortical Hyperfunction Associate 37388215
Bronchopulmonary Dysplasia Associate 39988826
Burkitt Lymphoma Associate 9689053
Carcinoma Hepatocellular Associate 36177006
Congenital Abnormalities Associate 8702008
Gigantism Associate 37388215
Growth hormone excess Associate 37388215
Growth Hormone Secreting Pituitary Adenoma Associate 38075079
Hypertension Associate 29162152
Insulin Resistance Associate 29162152