NP_001012123.1
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NCBI GenBank Nucleotide #
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UniProt Primary Accession #
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UniProt Related Accession #
Molecular Weight
25,334 Da
NCBI Official Full Name
complement C1q tumor necrosis factor-related protein 5
NCBI Official Synonym Full Names
C1q and tumor necrosis factor related protein 5
NCBI Protein Information
complement C1q tumor necrosis factor-related protein 5
UniProt Protein Name
Complement C1q tumor necrosis factor-related protein 5
UniProt Synonym Gene Names
UniProt Entry Name
C1QT5_RAT
UniProt Comments for C1QTNF5
C1QTNF5: Defects in C1QTNF5 are a cause of late-onset retinal degeneration (LORD). LORD is an autosomal dominant disorder characterized by onset in the fifth to sixth decade with night blindness and punctate yellow-white deposits in the retinal fundus, progressing to severe central and peripheral degeneration, with choroidal neovascularization and chorioretinal atrophy.
Protein type: Secreted; Secreted, signal peptide
Cellular Component: extracellular space; transport vesicle; collagen; tight junction; cell projection; membrane; cell; apical plasma membrane; plasma membrane; extracellular region; lateral plasma membrane
Molecular Function: identical protein binding
Biological Process: protein secretion; inner ear development
Research Articles on C1QTNF5
Precautions
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Disclaimer
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Diseases associated with C1QTNF5 elisa kit
Organs/Tissues associated with C1QTNF5 elisa kit
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