pleckstrin homology-like domain family B member 1 isoform X45 [Homo sa - Protein

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Biallelic frameshift variants in PHLDB1 cause mild-type osteogenesis imperfecta with regressive spondylometaphyseal changes. [J Med Genet. 2023]
Biallelic frameshift variants in PHLDB1 cause mild-type osteogenesis imperfecta with regressive spondylometaphyseal changes.
Tuysuz B, Uludag Alkaya D, Geyik F, Alaylıoğlu M, Kasap B, Kurugoğlu S, Akman YE, Vural M, Bilguvar K. J Med Genet. 2023 Aug; 60(8):819-826. Epub 2022 Dec 21.
A PHLDB1 variant associated with the nonfunctional pituitary adenoma. [J Neurooncol. 2019]
A PHLDB1 variant associated with the nonfunctional pituitary adenoma.
Kim LH, Kim JH, Namgoong S, Cheong HS, Yoon SJ, Kim EH, Kim SH, Kim SH, Chang JH, Shin HD. J Neurooncol. 2019 Apr; 142(2):223-229. Epub 2019 Mar 13.
Pleckstrin homology-like domain family B member 1 rs498872 polymorphism and glioma risk in Chinese Han population. [Cell Mol Biol (Noisy-le-grand)...]
Pleckstrin homology-like domain family B member 1 rs498872 polymorphism and glioma risk in Chinese Han population.
Zhang JW, Liu ZH, Lin XH, Du YP, Guo HT. Cell Mol Biol (Noisy-le-grand). 2017 Aug 30; 63(8):7-9. Epub 2017 Aug 30.

RefSeq mRNA
See reference mRNA sequence for the PHLDB1 gene (XM_047426636.1).
RefSeq protein isoforms
See 99 reference sequence protein isoforms for the PHLDB1 gene.

syndetin isoform c [Homo sapiens]
syndetin isoform c [Homo sapiens]
gi|384229074|ref|NP_001244927.1|

Protein
Homo sapiens cDNA FLJ44813 fis, clone BRACE3044495
Homo sapiens cDNA FLJ44813 fis, clone BRACE3044495
gi|34533376|dbj|AK126766.1|

Nucleotide

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Protein