Ferritin, heavy polypeptide-like 17 [Homo sapiens]

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Novel mutation in FTHL17 gene in pedigree with 46,XY pure gonadal dysgenesis. [Fertil Steril. 2019]
Novel mutation in FTHL17 gene in pedigree with 46,XY pure gonadal dysgenesis.
Tang R, Liu X, Pan L, Chen R. Fertil Steril. 2019 Jun; 111(6):1226-1235.e1. Epub 2019 Mar 25.
The Ferritin-Heavy-Polypeptide-Like-17 (FTHL17) gene encodes a ferritin with low stability and no ferroxidase activity and with a partial nuclear localization. [Biochim Biophys Acta. 2015]
The Ferritin-Heavy-Polypeptide-Like-17 (FTHL17) gene encodes a ferritin with low stability and no ferroxidase activity and with a partial nuclear localization.
Ruzzenenti P, Asperti M, Mitola S, Crescini E, Maccarinelli F, Gryzik M, Regoni M, Finazzi D, Arosio P, Poli M. Biochim Biophys Acta. 2015 Jun; 1850(6):1267-73. Epub 2015 Mar 5.
Severe XIST hypomethylation clearly distinguishes (SRY+) 46,XX-maleness from Klinefelter syndrome. [Eur J Endocrinol. 2010]
Severe XIST hypomethylation clearly distinguishes (SRY+) 46,XX-maleness from Klinefelter syndrome.
Poplinski A, Wieacker P, Kliesch S, Gromoll J. Eur J Endocrinol. 2010 Jan; 162(1):169-75. Epub 2009 Oct 7.

RefSeq genomic sequence
See the genomic reference sequence for the FTHL17 gene (NG_015850.1).
RefSeq protein
See the reference protein sequence for ferritin heavy polypeptide-like 17 (NP_114100.1).

Nucleotide
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Transcript/Protein Information [PANTHER Classification System]
Transcript/Protein Information
PANTHER Classification System
reagents [ExactAntigen/Labome]
reagents
ExactAntigen/Labome

Ferritin, heavy polypeptide-like 17 [Homo sapiens]
Ferritin, heavy polypeptide-like 17 [Homo sapiens]
gi|109172121|gb|AAI00771.1|

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