O09167.3
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UniProt Primary Accession #
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UniProt Related Accession #
Molecular Weight
18,562 Da
NCBI Official Full Name
60S ribosomal protein L21
NCBI Official Synonym Full Names
ribosomal protein L21
NCBI Protein Information
60S ribosomal protein L21
UniProt Protein Name
60S ribosomal protein L21
UniProt Entry Name
RL21_MOUSE
UniProt Comments for RPL21
RPL21: Defects in RPL21 are a cause of generalized hypotrichosis simplex (HTS). A rare form of non-syndromic hereditary hypotrichosis without characteristic hair shaft anomalies. Affected individuals typically show normal hair at birth, but hair loss and thinning of the hair shaft start during early childhood and progress with age. Belongs to the ribosomal protein L21e family.
Protein type: Ribosomal; Translation
Cellular Component: membrane; cytoplasm; nucleolus; ribosome; intracellular; ribonucleoprotein complex
Molecular Function: structural constituent of ribosome
Biological Process: translation
Research Articles on RPL21
Precautions
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Disclaimer
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Pathways associated with RPL21 elisa kit
Organs/Tissues associated with RPL21 elisa kit
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