Homo sapiens protein S (PROS1), transcript variant 2, mRNA

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PROS1 is a crucial gene in the macrophage efferocytosis of diabetic foot ulcers: a concerted analytical approach through the prisms of computer analysis. [Aging (Albany NY). 2024]
PROS1 is a crucial gene in the macrophage efferocytosis of diabetic foot ulcers: a concerted analytical approach through the prisms of computer analysis.
Shi H, Zhang Z, Yuan X, Liu G, Fan W, Wang W. Aging (Albany NY). 2024 Apr 10; 16(8):6883-6897. Epub 2024 Apr 10.
The Protein S Erlangen Mutation PROS1c.1904T>C (F635S) Suppresses Secretion. [Clin Lab. 2024]
The Protein S Erlangen Mutation PROS1c.1904T>C (F635S) Suppresses Secretion.
Reißig J, Cunningham S, Wandersee A, Brox R, Achenbach S, Strobel J, Hackstein H, Schneider S. Clin Lab. 2024 Mar 1; 70(3).
Analysis of PROS1 mutations and clinical characteristics in three Chinese families with hereditary protein S deficiency. [Ann Hematol. 2024]
Analysis of PROS1 mutations and clinical characteristics in three Chinese families with hereditary protein S deficiency.
Xu F, Zhou X, Jin Y, Yang L, Pan J, Wang M, Chen X. Ann Hematol. 2024 Feb; 103(2):653-662. Epub 2024 Jan 4.

RefSeq alternative splicing
See 3 reference mRNA sequence splice variants for the PROS1 gene.
RefSeq protein product
See the reference protein sequence for vitamin K-dependent protein S isoform 2 preproprotein (NP_000304.2).

Protein
Protein sequence from Nucleotide coding region
PubMed
PubMed articles cited by Nucleotide sequence record
Taxonomy
Taxonomy sequences associated with Nucleotide record
Annotated Genomic
Genomic sequence records that have the current RNA records as annotated features marking the exons of genes.
BioSystems
BioSystems
CCDS
Link to Consensus CDS
Components (Core)
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Full text in PMC
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Gene
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OMIM
OMIM records associated with Nucleotide sequence
Probe
Related Probe entry
PubMed (RefSeq)
Link to RefSeq PubMed articles
PubMed (Weighted)
Links to pubmed

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