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PRCC (gene)

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

Proline-rich protein PRCC is a protein that, in humans, is encoded by the PRCC gene.[5][6]

AliasesPRCC, RCCP1, TPRC, papillary renal cell carcinoma (translocation-associated), proline rich mitotic checkpoint control factor
External IDsOMIM: 179755; MGI: 2137738; GeneCards: PRCC
End156,800,815 bp[1]
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PRCC
Identifiers
AliasesPRCC, RCCP1, TPRC, papillary renal cell carcinoma (translocation-associated), proline rich mitotic checkpoint control factor
External IDsOMIM: 179755; MGI: 2137738; GeneCards: PRCC
Orthologs
DatabasesNCBI: entry; OMA: entry
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_005973
NM_199416

NM_033573

RefSeq (protein)

NP_005964

NP_291051

Location (UCSC)Chr 1: 156.75 – 156.8 MbChr 3: 87.77 – 87.79 Mb
PubMed search[3][4]
Wikidata
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In a subset of renal cell carcinomas, a t(X;1)(p11;q21) chromosome translocation has been repeatedly reported and is thought to be the cause of the cancer. As a result of the translocation, the transcription factor TFE3 on the X chromosome becomes fused to this gene on chromosome 1. The fused gene results in the fusion of N-terminal proline-rich region of the protein encoded by this gene to the entire TFE3 protein. This protein has been shown to interact with the mitotic checkpoint protein MAD2B, which suggests that the dominant-negative effect of the fusion protein with TFE3 may lead to a mitotic checkpoint defect. Alternatively spliced transcript variants encoding distinct isoforms have been observed.[6]

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