POF1B protein [Homo sapiens]

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A novel POF1B variant in a Chinese patient is associated with premature ovarian failure. [Clin Genet. 2021]
A novel POF1B variant in a Chinese patient is associated with premature ovarian failure.
Yuan ZZ, Wang CY, Jin JY, Sheng Y, Zhao MF, Fan LL, Zhang AQ. Clin Genet. 2021 Dec; 100(6):773-774. Epub 2021 Aug 23.
POF1B localizes to desmosomes and regulates cell adhesion in human intestinal and keratinocyte cell lines. [J Invest Dermatol. 2015]
POF1B localizes to desmosomes and regulates cell adhesion in human intestinal and keratinocyte cell lines.
Crespi A, Bertoni A, Ferrari I, Padovano V, Della Mina P, Berti E, Villa A, Pietrini G. J Invest Dermatol. 2015 Jan; 135(1):192-201. Epub 2014 Aug 1.
FISH characterization of the Xq21 breakpoint in a translocation carrier with premature ovarian failure. [Clin Genet. 1996]
FISH characterization of the Xq21 breakpoint in a translocation carrier with premature ovarian failure.
Riva P, Magnani I, Fuhrmann Conti AM, Gelli D, Sala C, Toniolo D, Larizza L. Clin Genet. 1996 Oct; 50(4):267-9.

RefSeq genomic sequence
See the genomic reference sequence for the POF1B gene (NG_016358.2).
RefSeq protein isoforms
See 4 reference sequence protein isoforms for the POF1B gene.

Nucleotide
Nucleotide sequence from coding region
PubMed
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Taxonomy
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Order cDNA clone
Order cDNA clone
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MODBASE, Database of Comparative Protein Structure Models (Sali Lab/UCSF) [MODBASE, Database of Comparat...]
MODBASE, Database of Comparative Protein Structure Models (Sali Lab/UCSF)
Transcript/Protein Information [PANTHER Classification System]
Transcript/Protein Information
PANTHER Classification System
reagents [ExactAntigen/Labome]
reagents
ExactAntigen/Labome

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Protein