Gene Gene information from NCBI Gene database.
Entrez ID 8985
Gene name Procollagen-lysine,2-oxoglutarate 5-dioxygenase 3
Gene symbol PLOD3
Synonyms (NCBI Gene)
BCARDLH3
Chromosome 7
Chromosome location 7q22.1
Summary The protein encoded by this gene is a membrane-bound homodimeric enzyme that is localized to the cisternae of the rough endoplasmic reticulum. The enzyme (cofactors iron and ascorbate) catalyzes the hydroxylation of lysyl residues in collagen-like peptide
SNPs SNP information provided by dbSNP.
5
SNP ID Visualize variation Clinical significance Consequence
rs121434414 T>C Pathogenic Missense variant, coding sequence variant
rs377320080 C>T Conflicting-interpretations-of-pathogenicity Missense variant, coding sequence variant
rs748105435 A>C Likely-pathogenic Stop gained, coding sequence variant
rs786205872 A>- Pathogenic Coding sequence variant, frameshift variant
rs1562894320 G>A Likely-pathogenic Coding sequence variant, missense variant
miRNA miRNA information provided by mirtarbase database.
92
miRTarBase ID miRNA Experiments Reference
MIRT000169 hsa-miR-21-5p Luciferase reporter assayQuantitative proteomic approach 19253296
MIRT002723 hsa-miR-124-3p Microarray 15685193
MIRT002723 hsa-miR-124-3p Proteomics;Microarray 18668037
MIRT002723 hsa-miR-124-3p Microarray 15685193
MIRT036230 hsa-miR-320b CLASH 23622248
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
57
GO ID Ontology Definition Evidence Reference
GO:0001701 Process In utero embryonic development IEA
GO:0001886 Process Endothelial cell morphogenesis IEA
GO:0003824 Function Catalytic activity IEA
GO:0005506 Function Iron ion binding EXP 30089812
GO:0005506 Function Iron ion binding IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
603066 9083 ENSG00000106397
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
O60568
Protein name Multifunctional procollagen lysine hydroxylase and glycosyltransferase LH3 [Includes: Procollagen-lysine,2-oxoglutarate 5-dioxygenase 3 (EC 1.14.11.4) (Lysyl hydroxylase 3) (LH3); Procollagen glycosyltransferase (EC 2.4.1.50) (EC 2.4.1.66) (Galactosylhydr
Protein function Multifunctional enzyme that catalyzes a series of essential post-translational modifications on Lys residues in procollagen (PubMed:11956192, PubMed:12475640, PubMed:18298658, PubMed:18834968, PubMed:30089812). Plays a redundant role in catalyzi
PDB 6FXK , 6FXM , 6FXR , 6FXT , 6FXX , 6FXY , 6TE3 , 6TEC , 6TES , 6TEU , 6TEX , 6TEZ , 6WFV , 8ONE
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF03171 2OG-FeII_Oxy 648 738 2OG-Fe(II) oxygenase superfamily Domain
Tissue specificity TISSUE SPECIFICITY: Ubiquitous (PubMed:9724729). Detected in heart, placenta and pancreas and at lower levels in lung, liver and skeletal muscle (PubMed:9582318, PubMed:9724729). {ECO:0000269|PubMed:9582318, ECO:0000269|PubMed:9724729}.
Sequence
MTSSGPGPRFLLLLPLLLPPAASASDRPRGRDPVNPEKLLVITVATAETEGYLRFLRSAE
FFNYTVRTLGLGEEWRGGDVARTVGGGQKVRWLKKEMEKYADREDMIIMFVDSYDVILAG
SPTELLKKFVQSGSRLLFSAESFCWPEWGLAEQYPEVGTGKRFLNSGGFIGFATTIHQIV
RQWKYKDDDDDQLFYTRLYLDPGLREKLSLNLDHKSRIFQNLNGALDEVVLKFDRNRVRI
RNVAYDTLPIVVHGNGPTKLQLNYLGNYVPNGWTPEGGCGFCNQDRRTLPGGQPPPRVFL
AVFVEQPTPFLPRFLQRLLLLDYPPDRVTLFLHNNEVFHEPHIADSWPQLQDHFSAVKLV
GPEEALSPGEARDMAMDLCRQDPECEFYFSLDADAVLTNLQTLRILIEENRKVIAPMLSR
HGKLWSNFWGALSPDEYYARSEDYVELVQRKRVGVWNVPYISQAYVIRGDTLRMELPQRD
VFSGSDTDPDMAFCKSFRDKGIFLHLSNQHEFGRLLATSRYDTEHLHPDLWQIFDNPVDW
KEQYIHENYSRALEGEGIVEQPCPDVYWFPLLSEQMCDELVAEMEHYGQWSGGRHEDSRL
AGGYENVPTVDIHMKQVGYEDQWLQLLRTYVGPMTESLFPGYHTKARAVMNFVVRYRPDE
QPSLRPHHDSSTFTLNVALNHKGLDYEGGGCRFLRYDCVISSPRKGWALLHPGRLTHYHE
GLPTTWGTRYIMVSFVDP
Sequence length 738
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  Reactome
  Lysine degradation
Other types of O-glycan biosynthesis
Metabolic pathways
  Collagen biosynthesis and modifying enzymes
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
18
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Causal Diseases associated with Pathogenic or Likely Pathogenic variants in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession Evidence Score
Bone fragility with contractures, arterial rupture, and deafness Pathogenic; Likely pathogenic rs1798091848, rs749921338, rs786205872, rs748105435, rs753360539, rs1562894320 RCV002250250
RCV003235768
RCV000007023
RCV000490386
RCV003990624
View all (1 more)
★★★★★
ClinVar: Pathogenic / Likely Pathogenic (≥5 Variants)
Neurodevelopmental delay Likely pathogenic rs1158167906 RCV002274425
★★★★☆
ClinVar: Pathogenic / Likely Pathogenic (<5 Variants)
PLOD3-related disorder Pathogenic rs749921338 RCV004550387
★★★★☆
ClinVar: Pathogenic / Likely Pathogenic (<5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
Acute myeloid leukemia Conflicting classifications of pathogenicity ClinVar
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
CEREBRAL AMYLOID ANGIOPATHY GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Cervical cancer Uncertain significance ClinVar
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Clear cell carcinoma of kidney Conflicting classifications of pathogenicity; Benign ClinVar
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Blister Blister Pubtator 30463024 Associate
★☆☆☆☆
Found in Text Mining only
Bone Fragility with Contractures, Arterial Rupture, and Deafness Bone Fragility With Contractures, Arterial Rupture, And Deafness UNIPROT_DG 18834968, 30089812, 30237576
★★★★★
ClinVar: Pathogenic / Likely Pathogenic (≥5 Variants)
Bone Fragility with Contractures, Arterial Rupture, and Deafness Bone Fragility With Contractures, Arterial Rupture, And Deafness GENOMICS_ENGLAND_DG 18834968
★★★★★
ClinVar: Pathogenic / Likely Pathogenic (≥5 Variants)
Bone Fragility with Contractures, Arterial Rupture, and Deafness Bone Fragility With Contractures, Arterial Rupture, And Deafness ORPHANET_DG 18834968
★★★★★
ClinVar: Pathogenic / Likely Pathogenic (≥5 Variants)
Bone Fragility with Contractures, Arterial Rupture, and Deafness Bone Fragility With Contractures, Arterial Rupture, And Deafness CLINVAR_DG 18834968
★★★★★
ClinVar: Pathogenic / Likely Pathogenic (≥5 Variants)
Bone Fragility with Contractures, Arterial Rupture, and Deafness Bone Fragility With Contractures, Arterial Rupture, And Deafness CTD_human_DG
★★★★★
ClinVar: Pathogenic / Likely Pathogenic (≥5 Variants)
Bronchopulmonary Dysplasia Bronchopulmonary Dysplasia BEFREE 24285264
★☆☆☆☆
Found in Text Mining only
Carcinogenesis Carcinogenesis Pubtator 34576068 Associate
★☆☆☆☆
Found in Text Mining only
Carcinoma Hepatocellular Hepatocellular carcinoma Pubtator 29397868, 31811111 Associate
★☆☆☆☆
Found in Text Mining only
Carcinoma of lung Lung carcinoma BEFREE 30442941, 30770789
★☆☆☆☆
Found in Text Mining only