chromosome 16 open reading frame 47 [Homo sapiens]

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ZFHX3 variants cause childhood partial epilepsy and infantile spasms with favourable outcomes. [J Med Genet. 2024]
ZFHX3 variants cause childhood partial epilepsy and infantile spasms with favourable outcomes.
He MF, Liu LH, Luo S, Wang J, Guo JJ, Wang PY, Zhai QX, He SL, Zou DF, Liu XR, et al. J Med Genet. 2024 Jun 20; 61(7):652-660. Epub 2024 Jun 20.
Haploinsufficiency of ZFHX3, encoding a key player in neuronal development, causes syndromic intellectual disability. [Am J Hum Genet. 2024]
Haploinsufficiency of ZFHX3, encoding a key player in neuronal development, causes syndromic intellectual disability.
Pérez Baca MDR, Jacobs EZ, Vantomme L, Leblanc P, Bogaert E, Dheedene A, De Cock L, Haghshenas S, Foroutan A, Levy MA, et al. Am J Hum Genet. 2024 Mar 7; 111(3):509-528. Epub 2024 Feb 26.
Adaptive Long-Read Sequencing Reveals GGC Repeat Expansion in ZFHX3 Associated with Spinocerebellar Ataxia Type 4. [Mov Disord. 2024]
Adaptive Long-Read Sequencing Reveals GGC Repeat Expansion in ZFHX3 Associated with Spinocerebellar Ataxia Type 4.
Chen Z, Gustavsson EK, Macpherson H, Anderson C, Clarkson C, Rocca C, Self E, Alvarez Jerez P, Scardamaglia A, Pellerin D, et al. Mov Disord. 2024 Mar; 39(3):486-497. Epub 2024 Jan 10.

RefSeq genomic sequence
See the genomic reference sequence for the ZFHX3 gene (NG_013211.2).
RefSeq protein isoforms
See 18 reference sequence protein isoforms for the ZFHX3 gene.

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

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