PLOD3 (procollagen-lysine,2-oxoglutarate 5-dioxygenase 3) - Chinchilla Research Resource Database
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Gene: PLOD3 (procollagen-lysine,2-oxoglutarate 5-dioxygenase 3) Homo sapiens
Analyze
Symbol: PLOD3
Name: procollagen-lysine,2-oxoglutarate 5-dioxygenase 3
CRRD ID: 1346467
Description: Exhibits procollagen galactosyltransferase activity; procollagen glucosyltransferase activity; and procollagen-lysine 5-dioxygenase activity. Involved in peptidyl-lysine hydroxylation and protein O-linked glycosylation. Localizes to Golgi apparatus and endoplasmic reticulum.
Type: protein-coding
RefSeq Status: REVIEWED
Also known as: LH3; lysine hydroxylase 3; lysyl hydroxlase 3; lysyl hydroxylase 3; multifunctional procollagen lysine hydroxylase and glycosyltransferase LH3; procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3
Orthologs:
Mus musculus (house mouse) : Plod3 (procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3)  MGI  Alliance
Rattus norvegicus (Norway rat) : Plod3 (procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3)  Alliance
Chinchilla lanigera (long-tailed chinchilla) : Plod3 (procollagen-lysine,2-oxoglutarate 5-dioxygenase 3)
Pan paniscus (bonobo/pygmy chimpanzee) : PLOD3 (procollagen-lysine,2-oxoglutarate 5-dioxygenase 3)
Canis lupus familiaris (dog) : PLOD3 (procollagen-lysine,2-oxoglutarate 5-dioxygenase 3)
Ictidomys tridecemlineatus (thirteen-lined ground squirrel) : Plod3 (procollagen-lysine,2-oxoglutarate 5-dioxygenase 3)
Sus scrofa (pig) : PLOD3 (procollagen-lysine,2-oxoglutarate 5-dioxygenase 3)
Chlorocebus sabaeus (African green monkey) : PLOD3 (procollagen-lysine,2-oxoglutarate 5-dioxygenase 3)
Heterocephalus glaber (naked mole-rat) : Plod3 (procollagen-lysine,2-oxoglutarate 5-dioxygenase 3)
more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl7101,205,977 - 101,218,420 (-)EnsemblGRCh38hg38GRCh38
GRCh387101,205,984 - 101,217,581 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh377100,849,258 - 100,861,011 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 367100,635,978 - 100,647,731 (-)NCBINCBI36hg18NCBI36
Build 347100,442,700 - 100,454,303NCBI
Celera795,858,417 - 95,870,169 (-)NCBI
Cytogenetic Map7q22.1NCBI
HuRef795,442,117 - 95,454,228 (-)NCBIHuRef
CHM1_17100,779,662 - 100,791,414 (-)NCBICHM1_1
CRA_TCAGchr7v27100,207,645 - 100,219,398 (-)NCBI
JBrowse: View Region in Genome Browser (JBrowse)
Model


Molecular Pathway Annotations     Click to see Annotation Detail View
References

Additional References at PubMed
PMID:9582318   PMID:9724729   PMID:10686427   PMID:10934207   PMID:11334715   PMID:11956192   PMID:12475640   PMID:12477932   PMID:12853948   PMID:15489334   PMID:16009940   PMID:16189514  
PMID:16303743   PMID:16447251   PMID:17314511   PMID:17643375   PMID:18187620   PMID:18298658   PMID:18834968   PMID:19056867   PMID:19156129   PMID:19199708   PMID:20562859   PMID:20955792  
PMID:21145461   PMID:21465473   PMID:21516116   PMID:21873635   PMID:21942715   PMID:22268729   PMID:22939629   PMID:23979707   PMID:25416956   PMID:25798074   PMID:25825495   PMID:25910212  
PMID:25921289   PMID:26028330   PMID:26344197   PMID:26380979   PMID:26496610   PMID:26598620   PMID:26638075   PMID:26972000   PMID:27233793   PMID:27342126   PMID:27371349   PMID:27435297  
PMID:27609421   PMID:27684187   PMID:27880917   PMID:28515276   PMID:28533407   PMID:28675297   PMID:29117863   PMID:29564676   PMID:29892012   PMID:30021884   PMID:30442941   PMID:30631154  
PMID:30770789   PMID:30775879   PMID:30833792   PMID:31067453   PMID:31129566   PMID:31317175   PMID:31446433   PMID:31515488   PMID:31527615   PMID:31536960   PMID:31586073   PMID:32296183  
PMID:33060197  


Genomics

Comparative Map Data
PLOD3
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl7101,205,977 - 101,218,420 (-)EnsemblGRCh38hg38GRCh38
GRCh387101,205,984 - 101,217,581 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh377100,849,258 - 100,861,011 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 367100,635,978 - 100,647,731 (-)NCBINCBI36hg18NCBI36
Build 347100,442,700 - 100,454,303NCBI
Celera795,858,417 - 95,870,169 (-)NCBI
Cytogenetic Map7q22.1NCBI
HuRef795,442,117 - 95,454,228 (-)NCBIHuRef
CHM1_17100,779,662 - 100,791,414 (-)NCBICHM1_1
CRA_TCAGchr7v27100,207,645 - 100,219,398 (-)NCBI
Plod3
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm395137,015,873 - 137,025,500 (+)NCBI
GRCm385136,987,019 - 136,996,646 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl5136,987,019 - 136,996,648 (+)EnsemblGRCm38mm10GRCm38
MGSCv375137,462,889 - 137,472,516 (+)NCBIGRCm37mm9NCBIm37
MGSCv365137,271,649 - 137,281,166 (+)NCBImm8
Celera5134,003,006 - 134,012,645 (+)NCBICelera
Cytogenetic Map5G2NCBI
cM Map576.09NCBI
Plod3
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Rnor_6.01222,716,421 - 22,726,982 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1222,716,423 - 22,726,982 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01224,728,205 - 24,738,766 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41220,856,527 - 20,867,088 (+)NCBIRGSC3.4rn4RGSC3.4
RGSC_v3.11220,846,399 - 20,856,690 (+)NCBI
Celera1221,452,299 - 21,462,860 (-)NCBICelera
Cytogenetic Map12q12NCBI
Plod3
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495545616,082,437 - 16,093,389 (+)EnsemblChiLan1.0
ChiLan1.0NW_00495545616,082,424 - 16,090,773 (+)NCBIChiLan1.0ChiLan1.0
PLOD3
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
PanPan1.17106,587,858 - 106,599,605 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl7106,587,858 - 106,599,605 (-)Ensemblpanpan1.1panPan2
Mhudiblu_PPA_v0793,347,335 - 93,358,921 (-)NCBIMhudiblu_PPA_v0panPan3
PLOD3
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1 Ensembl68,664,358 - 8,671,620 (+)EnsemblCanFam3.1canFam3CanFam3.1
CanFam3.168,664,135 - 8,671,637 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
Plod3
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
SpeTri2.0NW_0049365431,090,268 - 1,097,170 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
PLOD3
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl38,911,787 - 8,919,516 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.138,911,787 - 8,919,525 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
PLOD3
(Chlorocebus sabaeus - African green monkey)
Vervet AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1 Ensembl2811,962,286 - 11,975,228 (+)Ensembl
ChlSab1.12811,962,394 - 11,974,206 (+)NCBI
Plod3
(Heterocephalus glaber - naked mole-rat)
Molerat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla 1.0NW_00462474016,074,027 - 16,082,139 (+)NCBI

Position Markers
WI-8602  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377100,861,253 - 100,861,361UniSTSGRCh37
Build 367100,647,973 - 100,648,081RGDNCBI36
Celera795,870,411 - 95,870,519RGD
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map7q22UniSTS
HuRef795,454,470 - 95,454,578UniSTS
CRA_TCAGchr7v27100,219,640 - 100,219,748UniSTS
GeneMap99-GB4 RH Map7517.11UniSTS
Whitehead-RH Map7487.9UniSTS
PLOD3_8880  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377100,849,259 - 100,849,694UniSTSGRCh37
Build 367100,635,979 - 100,636,414RGDNCBI36
Celera795,858,418 - 95,858,853RGD
HuRef795,442,118 - 95,442,553UniSTS
CRA_TCAGchr7v27100,207,646 - 100,208,081UniSTS
A002S06  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377100,849,274 - 100,849,439UniSTSGRCh37
Build 367100,635,994 - 100,636,159RGDNCBI36
Celera795,858,433 - 95,858,598RGD
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map7q22UniSTS
HuRef795,442,133 - 95,442,298UniSTS
CRA_TCAGchr7v27100,207,661 - 100,207,826UniSTS
GeneMap99-GB4 RH Map7517.07UniSTS

miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:4545
Count of miRNA genes:1073
Interacting mature miRNAs:1378
Transcripts:ENST00000223127, ENST00000414785, ENST00000421736, ENST00000424135, ENST00000440925, ENST00000454310, ENST00000456079, ENST00000460132, ENST00000460475, ENST00000463479, ENST00000466881, ENST00000478082, ENST00000478264, ENST00000481461, ENST00000487563, ENST00000489927
Prediction methods:Microtar, Miranda, Rnahybrid, Targetscan
Result types:miRGate_prediction

The detailed report is available here: Full Report CSV TAB Printer

miRNA Target Status data imported from miRGate (http://mirgate.bioinfo.cnio.es/).
For more information about miRGate, see PMID:25858286 or access the full paper here.


Expression


RNA-SEQ Expression
High: > 1000 TPM value   Medium: Between 11 and 1000 TPM
Low: Between 0.5 and 10 TPM   Below Cutoff: < 0.5 TPM

alimentary part of gastrointestinal system circulatory system endocrine system exocrine system hemolymphoid system hepatobiliary system integumental system musculoskeletal system nervous system renal system reproductive system respiratory system sensory system visual system adipose tissue appendage entire extraembryonic component
High 5
Medium 2429 2467 1667 565 1439 418 3883 1630 2627 381 1438 1605 161 1204 2323 3
Low 3 517 56 57 509 46 467 563 1081 37 10 3 10 465 1
Below cutoff 1 1 2 1 5 1 8 2 2 1 1

Sequence

Nucleotide Sequences
RefSeq Transcripts NG_012148 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001084 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AC004876 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF046889 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF068229 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF207069 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK075338 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK297559 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK298537 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK312743 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL049952 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AY220458 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC011674 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC018946 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BF941815 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471197 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JC258727 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JC303366 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000223127   ⟹   ENSP00000223127
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl7101,205,984 - 101,217,581 (-)Ensembl
RefSeq Acc Id: ENST00000414785   ⟹   ENSP00000407551
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl7101,216,163 - 101,217,994 (-)Ensembl
RefSeq Acc Id: ENST00000421736   ⟹   ENSP00000407908
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl7101,210,595 - 101,216,020 (-)Ensembl
RefSeq Acc Id: ENST00000424135   ⟹   ENSP00000404799
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl7101,212,921 - 101,216,546 (-)Ensembl
RefSeq Acc Id: ENST00000440925   ⟹   ENSP00000394045
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl7101,210,128 - 101,211,915 (-)Ensembl
RefSeq Acc Id: ENST00000454310   ⟹   ENSP00000407555
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl7101,205,977 - 101,211,672 (-)Ensembl
RefSeq Acc Id: ENST00000456079   ⟹   ENSP00000416070
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl7101,216,521 - 101,218,420 (-)Ensembl
RefSeq Acc Id: ENST00000460132
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl7101,209,822 - 101,210,655 (-)Ensembl
RefSeq Acc Id: ENST00000460475
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl7101,211,635 - 101,212,976 (-)Ensembl
RefSeq Acc Id: ENST00000463479
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl7101,211,304 - 101,211,937 (-)Ensembl
RefSeq Acc Id: ENST00000466881
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl7101,210,356 - 101,211,103 (-)Ensembl
RefSeq Acc Id: ENST00000478082
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl7101,211,564 - 101,217,994 (-)Ensembl
RefSeq Acc Id: ENST00000478264
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl7101,212,544 - 101,213,555 (-)Ensembl
RefSeq Acc Id: ENST00000481461
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl7101,217,423 - 101,218,366 (-)Ensembl
RefSeq Acc Id: ENST00000487563
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl7101,208,593 - 101,210,439 (-)Ensembl
RefSeq Acc Id: ENST00000489927
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl7101,215,908 - 101,216,842 (-)Ensembl
RefSeq Acc Id: NM_001084   ⟹   NP_001075
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387101,205,984 - 101,217,581 (-)NCBI
GRCh377100,849,258 - 100,861,011 (-)ENTREZGENE
Build 367100,635,978 - 100,647,731 (-)NCBI Archive
HuRef795,442,117 - 95,454,228 (-)ENTREZGENE
CHM1_17100,779,662 - 100,791,414 (-)NCBI
CRA_TCAGchr7v27100,207,645 - 100,219,398 (-)ENTREZGENE
Sequence:
Reference Sequences
RefSeq Acc Id: NP_001075   ⟸   NM_001084
- Peptide Label: precursor
- UniProtKB: O60568 (UniProtKB/Swiss-Prot),   Q9UG85 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: ENSP00000404799   ⟸   ENST00000424135
RefSeq Acc Id: ENSP00000407551   ⟸   ENST00000414785
RefSeq Acc Id: ENSP00000394045   ⟸   ENST00000440925
RefSeq Acc Id: ENSP00000407555   ⟸   ENST00000454310
RefSeq Acc Id: ENSP00000416070   ⟸   ENST00000456079
RefSeq Acc Id: ENSP00000223127   ⟸   ENST00000223127
RefSeq Acc Id: ENSP00000407908   ⟸   ENST00000421736
Protein Domains
Fe2OG dioxygenase

Promoters
RGD ID:6806024
Promoter ID:HG_KWN:59026
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   K562,   Lymphoblastoid,   NB4
Transcripts:NM_001084,   OTTHUMT00000347471,   OTTHUMT00000347473,   OTTHUMT00000347474,   OTTHUMT00000347475,   OTTHUMT00000347476,   OTTHUMT00000347477,   OTTHUMT00000347478
Position:
Human AssemblyChrPosition (strand)Source
Build 367100,646,836 - 100,648,267 (-)MPROMDB
RGD ID:6850768
Promoter ID:EP73178
Type:initiation region
Name:HS_PLOD3
Description:Procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3.
SO ACC ID:SO:0000170
Source:EPD (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:NEDO full length human cDNA sequencing project.; Oligo-capping
Position:
Human AssemblyChrPosition (strand)Source
Build 367100,647,580 - 100,647,640EPD
RGD ID:7211459
Promoter ID:EPDNEW_H11475
Type:initiation region
Name:PLOD3_2
Description:procollagen-lysine,2-oxoglutarate 5-dioxygenase 3
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H11476  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh387101,217,355 - 101,217,415EPDNEW
RGD ID:7211461
Promoter ID:EPDNEW_H11476
Type:initiation region
Name:PLOD3_1
Description:procollagen-lysine,2-oxoglutarate 5-dioxygenase 3
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H11475  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh387101,217,581 - 101,217,641EPDNEW

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
NM_001084.5(PLOD3):c.2071del (p.Cys691fs) deletion Bone fragility with contractures, arterial rupture, and deafness [RCV000007023] Chr7:101206427 [GRCh38]
Chr7:100849708 [GRCh37]
Chr7:7q22.1
pathogenic
NM_001084.5(PLOD3):c.668A>G (p.Asn223Ser) single nucleotide variant Bone fragility with contractures, arterial rupture, and deafness [RCV000007022] Chr7:101215100 [GRCh38]
Chr7:100858381 [GRCh37]
Chr7:7q22.1
pathogenic
GRCh38/hg38 7p22.3-q36.3(chr7:53985-159282531)x1 copy number loss See cases [RCV000052250] Chr7:53985..159282531 [GRCh38]
Chr7:53985..159075220 [GRCh37]
Chr7:149068..158767981 [NCBI36]
Chr7:7p22.3-q36.3
pathogenic
GRCh38/hg38 7q21.3-22.1(chr7:98288474-101259804)x3 copy number gain See cases [RCV000053573] Chr7:98288474..101259804 [GRCh38]
Chr7:97917786..100903085 [GRCh37]
Chr7:97755722..100689805 [NCBI36]
Chr7:7q21.3-22.1
pathogenic
GRCh38/hg38 7q22.1(chr7:100419914-102482826)x1 copy number loss See cases [RCV000054155] Chr7:100419914..102482826 [GRCh38]
Chr7:100017537..102123273 [GRCh37]
Chr7:99855473..101910278 [NCBI36]
Chr7:7q22.1
pathogenic
NM_001084.4(PLOD3):c.1506C>T (p.Ile502=) single nucleotide variant Malignant melanoma [RCV000067550] Chr7:101210439 [GRCh38]
Chr7:100853720 [GRCh37]
Chr7:100640440 [NCBI36]
Chr7:7q22.1
not provided
GRCh38/hg38 7p22.3-q36.3(chr7:54185-159282390)x1 copy number loss See cases [RCV000135401] Chr7:54185..159282390 [GRCh38]
Chr7:54185..159075079 [GRCh37]
Chr7:149268..158767840 [NCBI36]
Chr7:7p22.3-q36.3
pathogenic
GRCh38/hg38 7q22.1(chr7:99195836-102258175)x1 copy number loss See cases [RCV000135782] Chr7:99195836..102258175 [GRCh38]
Chr7:98793459..101718950 [GRCh37]
Chr7:98631395..101688175 [NCBI36]
Chr7:7q22.1
pathogenic|uncertain significance
GRCh38/hg38 7q21.3-36.3(chr7:97419852-158923762)x3 copy number gain See cases [RCV000136717] Chr7:97419852..158923762 [GRCh38]
Chr7:97049164..158716453 [GRCh37]
Chr7:96887100..158409214 [NCBI36]
Chr7:7q21.3-36.3
pathogenic
GRCh38/hg38 7q22.1(chr7:101130561-101255628)x3 copy number gain See cases [RCV000136835] Chr7:101130561..101255628 [GRCh38]
Chr7:100773842..100898909 [GRCh37]
Chr7:100560562..100685629 [NCBI36]
Chr7:7q22.1
benign
GRCh38/hg38 7q22.1(chr7:99932610-102473188)x3 copy number gain See cases [RCV000138109] Chr7:99932610..102473188 [GRCh38]
Chr7:99530233..102113635 [GRCh37]
Chr7:99368169..101900640 [NCBI36]
Chr7:7q22.1
uncertain significance
NM_001084.5(PLOD3):c.1209G>A (p.Leu403=) single nucleotide variant not provided [RCV000756557] Chr7:101211869 [GRCh38]
Chr7:100855150 [GRCh37]
Chr7:7q22.1
likely benign
NM_001084.5(PLOD3):c.1993C>T (p.Arg665Trp) single nucleotide variant not provided [RCV000487905] Chr7:101206847 [GRCh38]
Chr7:100850128 [GRCh37]
Chr7:7q22.1
uncertain significance
NM_001084.5(PLOD3):c.1890T>G (p.Tyr630Ter) single nucleotide variant Bone fragility with contractures, arterial rupture, and deafness [RCV000490386] Chr7:101207623 [GRCh38]
Chr7:100850904 [GRCh37]
Chr7:7q22.1
likely pathogenic
NM_001084.5(PLOD3):c.1402C>G (p.Arg468Gly) single nucleotide variant Bone fragility with contractures, arterial rupture, and deafness [RCV000999838]|not provided [RCV000757674] Chr7:101210630 [GRCh38]
Chr7:100853911 [GRCh37]
Chr7:7q22.1
benign
NM_001084.5(PLOD3):c.2200T>A (p.Ser734Thr) single nucleotide variant not provided [RCV000757675] Chr7:101206298 [GRCh38]
Chr7:100849579 [GRCh37]
Chr7:7q22.1
uncertain significance
NM_001084.5(PLOD3):c.1355G>A (p.Arg452Gln) single nucleotide variant not provided [RCV000757676] Chr7:101211594 [GRCh38]
Chr7:100854875 [GRCh37]
Chr7:7q22.1
uncertain significance
NM_001084.5(PLOD3):c.1466C>T (p.Pro489Leu) single nucleotide variant not provided [RCV000757677] Chr7:101210566 [GRCh38]
Chr7:100853847 [GRCh37]
Chr7:7q22.1
uncertain significance
TMEM106B-BRAF fusion deletion Pleomorphic xanthoastrocytoma [RCV000454357] Chr7:12258147..140494267 [GRCh37]
Chr7:7p21.3-q34
pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:43360-159119707)x1 copy number loss See cases [RCV000446044] Chr7:43360..159119707 [GRCh37]
Chr7:7p22.3-q36.3
pathogenic
GRCh37/hg19 7q22.1-36.3(chr7:98969247-159119707)x3 copy number gain See cases [RCV000447709] Chr7:98969247..159119707 [GRCh37]
Chr7:7q22.1-36.3
pathogenic
NM_001084.5(PLOD3):c.887C>A (p.Pro296His) single nucleotide variant not provided [RCV000478234] Chr7:101212648 [GRCh38]
Chr7:100855929 [GRCh37]
Chr7:7q22.1
uncertain significance
GRCh37/hg19 7p22.3-q36.3(chr7:43361-159119707) copy number gain See cases [RCV000510686] Chr7:43361..159119707 [GRCh37]
Chr7:7p22.3-q36.3
pathogenic
NM_001084.5(PLOD3):c.1144G>C (p.Asp382His) single nucleotide variant Bone fragility with contractures, arterial rupture, and deafness [RCV000508323]|not provided [RCV000514263] Chr7:101211934 [GRCh38]
Chr7:100855215 [GRCh37]
Chr7:7q22.1
benign|likely benign
NM_001084.5(PLOD3):c.1006-5C>T single nucleotide variant not specified [RCV000508373] Chr7:101212379 [GRCh38]
Chr7:100855660 [GRCh37]
Chr7:7q22.1
likely benign
NM_001084.5(PLOD3):c.1977C>T (p.Asp659=) single nucleotide variant Bone fragility with contractures, arterial rupture, and deafness [RCV000505851] Chr7:101206863 [GRCh38]
Chr7:100850144 [GRCh37]
Chr7:7q22.1
benign
NM_001084.5(PLOD3):c.110-153T>C single nucleotide variant not specified [RCV000506505] Chr7:101216939 [GRCh38]
Chr7:100860220 [GRCh37]
Chr7:7q22.1
benign
NM_001084.5(PLOD3):c.1179C>T (p.Ala393=) single nucleotide variant Bone fragility with contractures, arterial rupture, and deafness [RCV000999780]|not provided [RCV000506522] Chr7:101211899 [GRCh38]
Chr7:100855180 [GRCh37]
Chr7:7q22.1
benign
NM_001084.5(PLOD3):c.503-9C>T single nucleotide variant not provided [RCV000894893]|not specified [RCV000506709] Chr7:101216029 [GRCh38]
Chr7:100859310 [GRCh37]
Chr7:7q22.1
likely benign
NM_001084.5(PLOD3):c.2171C>T (p.Thr724Met) single nucleotide variant not specified [RCV000506767] Chr7:101206327 [GRCh38]
Chr7:100849608 [GRCh37]
Chr7:7q22.1
uncertain significance
NM_001084.5(PLOD3):c.129T>C (p.Thr43=) single nucleotide variant not specified [RCV000506974] Chr7:101216767 [GRCh38]
Chr7:100860048 [GRCh37]
Chr7:7q22.1
likely benign
NM_001084.5(PLOD3):c.570C>T (p.Asp190=) single nucleotide variant Bone fragility with contractures, arterial rupture, and deafness [RCV000507249] Chr7:101215953 [GRCh38]
Chr7:100859234 [GRCh37]
Chr7:7q22.1
benign
NM_001084.5(PLOD3):c.1528C>T (p.His510Tyr) single nucleotide variant not provided [RCV000507284] Chr7:101210417 [GRCh38]
Chr7:100853698 [GRCh37]
Chr7:7q22.1
benign
NM_001084.5(PLOD3):c.1935+105T>G single nucleotide variant Bone fragility with contractures, arterial rupture, and deafness [RCV000507552] Chr7:101207473 [GRCh38]
Chr7:100850754 [GRCh37]
Chr7:7q22.1
likely benign
NM_001084.5(PLOD3):c.1233-4G>A single nucleotide variant Bone fragility with contractures, arterial rupture, and deafness [RCV000508024] Chr7:101211720 [GRCh38]
Chr7:100855001 [GRCh37]
Chr7:7q22.1
benign
NM_001084.5(PLOD3):c.123G>A (p.Val41=) single nucleotide variant not provided [RCV000508101] Chr7:101216773 [GRCh38]
Chr7:100860054 [GRCh37]
Chr7:7q22.1
benign
GRCh37/hg19 7p22.3-q36.3(chr7:43361-159119707)x3 copy number gain See cases [RCV000511549] Chr7:43361..159119707 [GRCh37]
Chr7:7p22.3-q36.3
pathogenic
NM_001084.5(PLOD3):c.1636C>A (p.His546Asn) single nucleotide variant not provided [RCV000513344] Chr7:101210140 [GRCh38]
Chr7:100853421 [GRCh37]
Chr7:7q22.1
uncertain significance
NM_001084.5(PLOD3):c.502+4A>G single nucleotide variant not provided [RCV000513555] Chr7:101216159 [GRCh38]
Chr7:100859440 [GRCh37]
Chr7:7q22.1
uncertain significance
NM_001084.5(PLOD3):c.887C>G (p.Pro296Arg) single nucleotide variant Bone fragility with contractures, arterial rupture, and deafness [RCV001001983]|not provided [RCV000659081] Chr7:101212648 [GRCh38]
Chr7:100855929 [GRCh37]
Chr7:7q22.1
uncertain significance
NM_001084.5(PLOD3):c.2137G>A (p.Gly713Ser) single nucleotide variant not provided [RCV000659080] Chr7:101206361 [GRCh38]
Chr7:100849642 [GRCh37]
Chr7:7q22.1
uncertain significance
Single allele duplication Congenital plasminogen activator inhibitor type 1 deficiency [RCV000677965] Chr7:100730280..100853730 [GRCh37]
Chr7:7q22.1
uncertain significance
GRCh37/hg19 7q22.1(chr7:98847725-102472176)x1 copy number loss not provided [RCV000682904] Chr7:98847725..102472176 [GRCh37]
Chr7:7q22.1
pathogenic
GRCh37/hg19 7q22.1-36.3(chr7:98693388-159119707)x3 copy number gain not provided [RCV000682911] Chr7:98693388..159119707 [GRCh37]
Chr7:7q22.1-36.3
pathogenic
NC_000007.13:g.(20954043_21001537)_(114528369_114556605)inv inversion Speech-language disorder 1 [RCV000234948] Chr7:21001537..114528369 [GRCh37]
Chr7:7p15.3-q31.1
pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:44935-159126310)x3 copy number gain not provided [RCV000746280] Chr7:44935..159126310 [GRCh37]
Chr7:7p22.3-q36.3
pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:10704-159122532)x3 copy number gain not provided [RCV000746278] Chr7:10704..159122532 [GRCh37]
Chr7:7p22.3-q36.3
pathogenic
NM_001084.5(PLOD3):c.1812C>T (p.Tyr604=) single nucleotide variant not provided [RCV000896585] Chr7:101207701 [GRCh38]
Chr7:100850982 [GRCh37]
Chr7:7q22.1
likely benign
NM_001084.5(PLOD3):c.809C>T (p.Pro270Leu) single nucleotide variant Bone fragility with contractures, arterial rupture, and deafness [RCV000761553] Chr7:101212912 [GRCh38]
Chr7:100856193 [GRCh37]
Chr7:7q22.1
likely pathogenic
NM_001084.5(PLOD3):c.1939C>T (p.Arg647Trp) single nucleotide variant not provided [RCV000762469] Chr7:101206901 [GRCh38]
Chr7:100850182 [GRCh37]
Chr7:7q22.1
uncertain significance
NM_001084.5(PLOD3):c.1678G>C (p.Glu560Gln) single nucleotide variant Bone fragility with contractures, arterial rupture, and deafness [RCV001002170]|not provided [RCV000762470] Chr7:101210098 [GRCh38]
Chr7:100853379 [GRCh37]
Chr7:7q22.1
benign|likely benign
NM_001084.5(PLOD3):c.1675G>A (p.Val559Met) single nucleotide variant not provided [RCV000762471] Chr7:101210101 [GRCh38]
Chr7:100853382 [GRCh37]
Chr7:7q22.1
uncertain significance
NM_001084.5(PLOD3):c.2172G>C (p.Thr724=) single nucleotide variant not provided [RCV000947053] Chr7:101206326 [GRCh38]
Chr7:100849607 [GRCh37]
Chr7:7q22.1
likely benign
NM_001084.5(PLOD3):c.1797G>A (p.Arg599=) single nucleotide variant Bone fragility with contractures, arterial rupture, and deafness [RCV001000253]|not provided [RCV000950416] Chr7:101207716 [GRCh38]
Chr7:100850997 [GRCh37]
Chr7:7q22.1
benign
NM_001084.5(PLOD3):c.201+10G>A single nucleotide variant not provided [RCV000900622] Chr7:101216685 [GRCh38]
Chr7:100859966 [GRCh37]
Chr7:7q22.1
benign
NM_001084.5(PLOD3):c.109+10C>T single nucleotide variant not provided [RCV000981188] Chr7:101217156 [GRCh38]
Chr7:100860437 [GRCh37]
Chr7:7q22.1
likely benign
NM_001084.5(PLOD3):c.2124A>G (p.Ala708=) single nucleotide variant not provided [RCV000924195] Chr7:101206374 [GRCh38]
Chr7:100849655 [GRCh37]
Chr7:7q22.1
benign
NM_001084.5(PLOD3):c.147C>T (p.Thr49=) single nucleotide variant not provided [RCV000883936] Chr7:101216749 [GRCh38]
Chr7:100860030 [GRCh37]
Chr7:7q22.1
likely benign
NM_001084.5(PLOD3):c.1006-4C>T single nucleotide variant not provided [RCV000976147] Chr7:101212378 [GRCh38]
Chr7:100855659 [GRCh37]
Chr7:7q22.1
likely benign
NM_001084.5(PLOD3):c.1692G>A (p.Pro564=) single nucleotide variant not provided [RCV000942052] Chr7:101208949 [GRCh38]
Chr7:100852230 [GRCh37]
Chr7:7q22.1
likely benign
NM_001084.5(PLOD3):c.988C>G (p.Leu330Val) single nucleotide variant not provided [RCV000906535] Chr7:101212547 [GRCh38]
Chr7:100855828 [GRCh37]
Chr7:7q22.1
benign
NM_001084.5(PLOD3):c.1164C>T (p.Tyr388=) single nucleotide variant not provided [RCV000898826] Chr7:101211914 [GRCh38]
Chr7:100855195 [GRCh37]
Chr7:7q22.1
likely benign
NM_001084.5(PLOD3):c.1756C>G (p.His586Asp) single nucleotide variant not provided [RCV000922473] Chr7:101208885 [GRCh38]
Chr7:100852166 [GRCh37]
Chr7:7q22.1
likely benign
GRCh37/hg19 7p22.3-q36.3(chr7:10365-159119707)x3 copy number gain not provided [RCV000848126] Chr7:10365..159119707 [GRCh37]
Chr7:7p22.3-q36.3
pathogenic
NM_001084.5(PLOD3):c.2004C>T (p.His668=) single nucleotide variant not provided [RCV000910438] Chr7:101206836 [GRCh38]
Chr7:100850117 [GRCh37]
Chr7:7q22.1
likely benign
NM_001084.5(PLOD3):c.1887G>A (p.Thr629=) single nucleotide variant not provided [RCV000963888] Chr7:101207626 [GRCh38]
Chr7:100850907 [GRCh37]
Chr7:7q22.1
likely benign
NM_001084.5(PLOD3):c.294G>A (p.Glu98=) single nucleotide variant not provided [RCV000977879] Chr7:101216454 [GRCh38]
Chr7:100859735 [GRCh37]
Chr7:7q22.1
likely benign
NM_001084.5(PLOD3):c.535A>G (p.Ile179Val) single nucleotide variant not provided [RCV000968615] Chr7:101215988 [GRCh38]
Chr7:100859269 [GRCh37]
Chr7:7q22.1
benign
NM_001084.5(PLOD3):c.804C>T (p.Tyr268=) single nucleotide variant not provided [RCV000964291] Chr7:101212917 [GRCh38]
Chr7:100856198 [GRCh37]
Chr7:7q22.1
benign
NM_001084.5(PLOD3):c.453G>A (p.Ala151=) single nucleotide variant not provided [RCV000901107] Chr7:101216212 [GRCh38]
Chr7:100859493 [GRCh37]
Chr7:7q22.1
likely benign
NM_001084.5(PLOD3):c.1500+8C>T single nucleotide variant not provided [RCV000963351] Chr7:101210524 [GRCh38]
Chr7:100853805 [GRCh37]
Chr7:7q22.1
likely benign
NM_001084.5(PLOD3):c.975C>T (p.Pro325=) single nucleotide variant not provided [RCV000893676] Chr7:101212560 [GRCh38]
Chr7:100855841 [GRCh37]
Chr7:7q22.1
benign
NM_001084.5(PLOD3):c.961C>T (p.Leu321=) single nucleotide variant not provided [RCV000897392] Chr7:101212574 [GRCh38]
Chr7:100855855 [GRCh37]
Chr7:7q22.1
likely benign
NM_001084.5(PLOD3):c.1323C>T (p.Ser441=) single nucleotide variant not provided [RCV000920415] Chr7:101211626 [GRCh38]
Chr7:100854907 [GRCh37]
Chr7:7q22.1
likely benign
NM_001084.5(PLOD3):c.335A>G (p.Asp112Gly) single nucleotide variant not provided [RCV000998872] Chr7:101216413 [GRCh38]
Chr7:100859694 [GRCh37]
Chr7:7q22.1
uncertain significance
NM_001084.5(PLOD3):c.1315G>A (p.Ala439Thr) single nucleotide variant not provided [RCV000885205] Chr7:101211634 [GRCh38]
Chr7:100854915 [GRCh37]
Chr7:7q22.1
likely benign
NM_001084.5(PLOD3):c.1176C>T (p.Asp392=) single nucleotide variant not provided [RCV000933537] Chr7:101211902 [GRCh38]
Chr7:100855183 [GRCh37]
Chr7:7q22.1
likely benign
NM_001084.5(PLOD3):c.54G>T (p.Leu18=) single nucleotide variant not provided [RCV000932660] Chr7:101217221 [GRCh38]
Chr7:100860502 [GRCh37]
Chr7:7q22.1
likely benign
NM_001084.5(PLOD3):c.477G>A (p.Thr159=) single nucleotide variant not provided [RCV000909311] Chr7:101216188 [GRCh38]
Chr7:100859469 [GRCh37]
Chr7:7q22.1
likely benign
NM_001084.5(PLOD3):c.1904C>T (p.Thr635Ile) single nucleotide variant not provided [RCV000907413] Chr7:101207609 [GRCh38]
Chr7:100850890 [GRCh37]
Chr7:7q22.1
likely benign
NM_001084.5(PLOD3):c.1695C>T (p.Asp565=) single nucleotide variant not provided [RCV000899315] Chr7:101208946 [GRCh38]
Chr7:100852227 [GRCh37]
Chr7:7q22.1
likely benign
NM_001084.5(PLOD3):c.805G>A (p.Val269Ile) single nucleotide variant not provided [RCV000933389] Chr7:101212916 [GRCh38]
Chr7:100856197 [GRCh37]
Chr7:7q22.1
likely benign|conflicting interpretations of pathogenicity
NM_001084.5(PLOD3):c.735C>T (p.Tyr245=) single nucleotide variant not provided [RCV000888516] Chr7:101213149 [GRCh38]
Chr7:100856430 [GRCh37]
Chr7:7q22.1
benign
NM_001084.5(PLOD3):c.615+9G>A single nucleotide variant not provided [RCV000938990] Chr7:101215899 [GRCh38]
Chr7:100859180 [GRCh37]
Chr7:7q22.1
likely benign
NM_001084.5(PLOD3):c.740C>T (p.Thr247Met) single nucleotide variant not provided [RCV000956514] Chr7:101213144 [GRCh38]
Chr7:100856425 [GRCh37]
Chr7:7q22.1
likely benign
NM_001084.5(PLOD3):c.1986G>A (p.Pro662=) single nucleotide variant Bone fragility with contractures, arterial rupture, and deafness [RCV001000300]|not provided [RCV000890104] Chr7:101206854 [GRCh38]
Chr7:100850135 [GRCh37]
Chr7:7q22.1
benign
NM_001084.5(PLOD3):c.1233-5C>T single nucleotide variant not provided [RCV000934306] Chr7:101211721 [GRCh38]
Chr7:100855002 [GRCh37]
Chr7:7q22.1
likely benign
NM_001084.5(PLOD3):c.1290C>T (p.Gly430=) single nucleotide variant not provided [RCV000890710] Chr7:101211659 [GRCh38]
Chr7:100854940 [GRCh37]
Chr7:7q22.1
likely benign
NM_001084.5(PLOD3):c.634C>T (p.Leu212=) single nucleotide variant not provided [RCV000890796] Chr7:101215134 [GRCh38]
Chr7:100858415 [GRCh37]
Chr7:7q22.1
likely benign
NM_001084.5(PLOD3):c.1684C>T (p.Pro562Ser) single nucleotide variant Bone fragility with contractures, arterial rupture, and deafness [RCV001169951] Chr7:101208957 [GRCh38]
Chr7:100852238 [GRCh37]
Chr7:7q22.1
uncertain significance
GRCh37/hg19 7q22.1(chr7:99593346-102470275)x1 copy number loss See cases [RCV001195072] Chr7:99593346..102470275 [GRCh37]
Chr7:7q22.1
likely pathogenic
NM_001084.5(PLOD3):c.560A>G (p.Asp187Gly) single nucleotide variant PLOD3-Related Disorder [RCV001249438] Chr7:101215963 [GRCh38]
Chr7:100859244 [GRCh37]
Chr7:7q22.1
not provided

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:9083 AgrOrtholog
COSMIC PLOD3 COSMIC
Ensembl Genes ENSG00000106397 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Protein ENSP00000223127 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000394045 UniProtKB/TrEMBL
  ENSP00000404799 UniProtKB/TrEMBL
  ENSP00000407551 UniProtKB/TrEMBL
  ENSP00000407555 UniProtKB/TrEMBL
  ENSP00000407908 UniProtKB/TrEMBL
  ENSP00000416070 UniProtKB/TrEMBL
Ensembl Transcript ENST00000223127 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000414785 UniProtKB/TrEMBL
  ENST00000421736 UniProtKB/TrEMBL
  ENST00000424135 UniProtKB/TrEMBL
  ENST00000440925 UniProtKB/TrEMBL
  ENST00000454310 UniProtKB/TrEMBL
  ENST00000456079 UniProtKB/TrEMBL
GTEx ENSG00000106397 GTEx
HGNC ID HGNC:9083 ENTREZGENE
Human Proteome Map PLOD3 Human Proteome Map
InterPro Nucleotide-diphossugar_trans UniProtKB/Swiss-Prot
  Oxoglu/Fe-dep_dioxygenase UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Pro_4_hyd_alph UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Procol_lys_dOase UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:8985 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
NCBI Gene 8985 ENTREZGENE
OMIM 603066 OMIM
  612394 OMIM
Pfam 2OG-FeII_Oxy UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA33413 PharmGKB
PROSITE FE2OG_OXY UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  LYS_HYDROXYLASE UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART P4Hc UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF53448 UniProtKB/Swiss-Prot
UniGene Hs.153357 ENTREZGENE
UniProt C9JIX5_HUMAN UniProtKB/TrEMBL
  C9JU11_HUMAN UniProtKB/TrEMBL
  H7C0B8_HUMAN UniProtKB/TrEMBL
  H7C2A8_HUMAN UniProtKB/TrEMBL
  H7C2S8_HUMAN UniProtKB/TrEMBL
  H7C2V1_HUMAN UniProtKB/TrEMBL
  O60568 ENTREZGENE, UniProtKB/Swiss-Prot
  Q9UG85 ENTREZGENE, UniProtKB/TrEMBL
UniProt Secondary B2R6W6 UniProtKB/Swiss-Prot
  Q540C3 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2016-04-12 PLOD3  procollagen-lysine,2-oxoglutarate 5-dioxygenase 3    procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3  Symbol and/or name change 5135510 APPROVED
2011-08-17 PLOD3  procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3  PLOD3  procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3  Symbol and/or name change 5135510 APPROVED