PLET1 | |||||||||||||||||||||||||||||||||||||||||||||||||||
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Aliases | PLET1 , C11orf34, placenta expressed transcript 1 | ||||||||||||||||||||||||||||||||||||||||||||||||||
External IDs | OMIM: 611904 MGI: 1923759 HomoloGene: 49928 GeneCards: PLET1 | ||||||||||||||||||||||||||||||||||||||||||||||||||
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Wikidata | |||||||||||||||||||||||||||||||||||||||||||||||||||
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Placenta expressed transcript 1 is a protein that in humans is encoded by the PLET1 gene. [5]
Epigen also known as epithelial mitogen is a protein that in humans is encoded by the EPGN gene.
Putative P2Y purinoceptor 10 is a protein that, in humans, is encoded by the P2RY10 gene.
Transcriptional enhancer factor TEF-5 is a protein that in humans is encoded by the TEAD3 gene.
Solute carrier organic anion transporter family member 3A1 is a protein that in humans is encoded by the SLCO3A1 gene.
Dynein, axonemal, heavy chain 7 is a protein in humans that is encoded by the DNAH7 gene.
Calpain-6 is a protein in humans that is encoded by the CAPN6 gene.
Calcium/calmodulin-dependent protein kinase ID is a protein in humans that is encoded by the CAMK1D gene on chromosome 10.
Monocarboxylate transporter 6 (MCT6) is a protein in humans that is encoded by the SLC16A5 gene.
Zinc finger protein 280B is a protein that in humans is encoded by the ZNF280B gene.
Tripartite motif containing 69 is a protein that in humans is encoded by the TRIM69 gene.
Lin-28 homolog B is a protein that in humans is encoded by the LIN28B gene.
Fanconi Anemia Opposite Strand Transcript protein is a predicted protein that in humans is encoded by the FANCD2OS gene. The name is derived from mRNA transcribed from the strand complementary to the FANCD2 gene.
RTL1 is a retrotransposon derived protein coding gene. It is also known as PEG11 and is a paternally expressed imprinted gene, part of genomic imprinting. RTL1 plays an important role in the maintenance of fetal capillaries and is expressed in high quantities during late stage of fetal development. The expression of this gene is important for the development of the placenta, the fetus-maternal interface. Because the placenta is the first organ to form during the development of an embryo, problems in its establishment and biological role lead to complications during gestation. This organ maintains the fetus throughout the pregnancy and is therefore sensitive to disruptions. Studies in mice suggest that disruption of the RTL1 concentration, whether increasing or decreasing the amount of this protein coding gene, can lead to serious errors in the conservation of placental fetal capillaries. RTL1 knockout mice have shown obstruction in fetal development along with late fetal/neonatal death. Studies from sheep homologs suggest that high expression levels of RTL1 can lead to skeletal muscle hypertrophy This is due to over-expression patterns in the paternal allele specific gene.
Progesterone receptor membrane component 2 is a protein which is encoded by the PGRMC2 gene. It has been detected in the placenta, liver, and spermatozoa, among other areas.
Solute carrier family 38 member 5 is a protein that in humans is encoded by the SLC38A5 gene.
Chromosome 15 open reading frame 48 is a protein that in humans is encoded by the C15orf48 gene.
Shroom family member 2 is a protein that in humans is encoded by the SHROOM2 gene.
Serine protease 55 is a protein that in humans is encoded by the PRSS55 gene.
Endonuclease, poly(U) specific is a protein that in humans is encoded by the ENDOU gene.
Forkhead box protein F2 is a protein that in humans is encoded by the FOXF2 gene.