PLLP, plasmolipin, 51090

N. diseases: 10; N. variants: 3
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0345967
Disease: Malignant mesothelioma
Malignant mesothelioma
0.300 Biomarker disease CTD_human MicroRNA and mRNA features of malignant pleural mesothelioma and benign asbestos-related pleural effusion. 25756049 2015
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.300 Biomarker disease PSYGENET Among the most consistent changes in genes with robust expression were significant decreases in the expression of myelination-related genes MAG, PLLP (TM4SF11), PLP1, ERBB3 in subjects with schizophrenia. 15334603 2004
Corpuscular Hemoglobin Concentration Mean
0.100 GeneticVariation phenotype GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010 2018
CUI: C0854723
Disease: Retinal Dystrophies
Retinal Dystrophies
0.100 GeneticVariation group CLINVAR
RETINITIS PIGMENTOSA 82 WITH OR WITHOUT SITUS INVERSUS
0.100 CausalMutation disease CLINVAR
CUI: C0022578
Disease: Keratoconus
Keratoconus
0.010 Biomarker disease BEFREE We also identified plasmolipin and Notch1 as being significantly reduced in keratoconus for both gene and protein expression (p < 0.05). 29321650 2018
CUI: C0042769
Disease: Virus Diseases
Virus Diseases
0.010 Biomarker group BEFREE Plasmolipin, PmPLP1, from Penaeus monodon is a potential receptor for yellow head virus infection. 30031867 2018
CUI: C0270922
Disease: Peripheral demyelinating neuropathy
Peripheral demyelinating neuropathy
0.010 Biomarker disease BEFREE Plasmolipin is a membrane protein and belongs to the tetraspan molecule (4TM) family, an expanding group of myelin proteins many of which could be linked to human hereditary demyelinating neuropathies. 11707781 2001
CUI: C0752166
Disease: Bardet-Biedl Syndrome
Bardet-Biedl Syndrome
0.010 GeneticVariation disease BEFREE By means of radiation hybrid mapping and FISH analysis, we could localize the human plasmolipin gene to Chromosome 16q13 within the putative region of the Bardet-Biedl syndrome type 2 (BBS2) gene locus. 11707781 2001
CUI: C2936863
Disease: Bardet-Biedl syndrome 2 (disorder)
Bardet-Biedl syndrome 2 (disorder)
0.010 Biomarker disease BEFREE With respect to intrafamiliar variations in the manifestation of BBS, we suggest that plasmolipin might be either another candidate gene or a modifier of the BBS2 phenotype. 11707781 2001