Homo sapiens paired immunoglobin like type 2 receptor alpha (PILRA), R - Nucleotide

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New candidate SNPs for genetic association with Alzheimer's disease: a linkage disequilibrium analysis for the FCGRIIB and PILRA genes. [Medwave. 2024]
New candidate SNPs for genetic association with Alzheimer's disease: a linkage disequilibrium analysis for the FCGRIIB and PILRA genes.
Levi-Monsalve A, Flores SV, Manriquez G, Roco-Videla Á. Medwave. 2024 Feb 26; 24(1). Epub 2024 Feb 26.
A loss-of-function variant in ZCWPW1 causes human male infertility with sperm head defect and high DNA fragmentation. [Reprod Health. 2024]
A loss-of-function variant in ZCWPW1 causes human male infertility with sperm head defect and high DNA fragmentation.
Song Y, Guo J, Zhou Y, Wei X, Li J, Zhang G, Wang H. Reprod Health. 2024 Feb 3; 21(1):18. Epub 2024 Feb 3.
The histone modification reader ZCWPW1 promotes double-strand break repair by regulating cross-talk of histone modifications and chromatin accessibility at meiotic hotspots. [Genome Biol. 2022]
The histone modification reader ZCWPW1 promotes double-strand break repair by regulating cross-talk of histone modifications and chromatin accessibility at meiotic hotspots.
Yuan S, Huang T, Bao Z, Wang S, Wu X, Liu J, Liu H, Chen ZJ. Genome Biol. 2022 Sep 6; 23(1):187. Epub 2022 Sep 6.

RefSeq alternative splicing
See 7 reference mRNA sequence splice variants for the PILRA gene.

Protein
Protein sequence from Nucleotide coding region
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RNA
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Nucleotide