Homo sapiens serine protease 56 (PRSS56), RefSeqGene on chromosome 2

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CHRND variant in a paternally inherited esophageal atresia and tracheoesophgageal fistula: Report of a case. [Birth Defects Res. 2024]
CHRND variant in a paternally inherited esophageal atresia and tracheoesophgageal fistula: Report of a case.
Soyer T, Boybeyi Ö, Karaosmanoğlu B, Taşkıran E, Şimşek ÖP, Utine GE. Birth Defects Res. 2024 Jan; 116(1):e2286. Epub 2023 Dec 12.
Pathogenic variants of MFRP and PRSS56 genes are major causes of nanophthalmos in Japanese patients. [Ophthalmic Genet. 2023]
Pathogenic variants of MFRP and PRSS56 genes are major causes of nanophthalmos in Japanese patients.
Ota J, Inooka T, Okado S, Maeda N, Koyanagi Y, Kominami T, Nishiguchi KM, Ueno S. Ophthalmic Genet. 2023 Oct; 44(5):423-429. Epub 2023 Jul 28.
MYC multimers shield stalled replication forks from RNA polymerase. [Nature. 2022]
MYC multimers shield stalled replication forks from RNA polymerase.
Solvie D, Baluapuri A, Uhl L, Fleischhauer D, Endres T, Papadopoulos D, Aziba A, Gaballa A, Mikicic I, Isaakova E, et al. Nature. 2022 Dec; 612(7938):148-155. Epub 2022 Nov 23.

RefSeq alternative splicing
See 4 reference mRNA sequence splice variants for the PRSS56 gene.

Protein
Protein sequence from Nucleotide coding region
PubMed
PubMed articles cited by Nucleotide sequence record
Taxonomy
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Full text in PMC
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OMIM
OMIM records associated with Nucleotide sequence
PubMed (Weighted)
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RNA
RNA sequence records that are annotated on the current genomic nucleotide sequences. The RNA records represent aligned or predicted transcripts of the current records.
SNP
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Nucleotide