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GPR162

GPR162 (G Protein-Coupled Receptor 162) is a Protein Coding gene. Diseases associated with GPR162 include Fanconi Anemia, Complementation Group C and Vitreous Detachment. Among its related pathways are "GPCRs, other". Gene Ontology (GO) annotations related to this gene include G protein-coupled receptor activity. An important paralog of this gene is GPR153.
Protein class

G-protein coupled receptors

Predicted location

Intracellular, Membrane (different isoforms)

Single cell type specificity

Cell type enhanced (Bipolar cells, Respiratory ciliated cells, Muller glia cells, Horizontal cells, Excitatory neurons, Inhibitory neurons)

Immune cell specificity

Group enriched (neutrophil, classical monocyte, intermediate monocyte)

Cell line specificity

Cell line enhanced (AF22, AN3-CA, hTERT-RPE1, NTERA-2, SH-SY5Y, U-2 OS)

Molecular function

G-protein coupled receptor, Receptor, Transducer

More Types Infomation

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For Research Use Only. Not For Clinical Use.

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