gamma-tubulin complex component 2 isoform 3 [Homo sapiens]

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Autosomal recessive variants in TUBGCP2 alter the γ-tubulin ring complex leading to neurodevelopmental disease. [iScience. 2021]
Autosomal recessive variants in TUBGCP2 alter the γ-tubulin ring complex leading to neurodevelopmental disease.
Gungor S, Oktay Y, Hiz S, Aranguren-Ibáñez Á, Kalafatcilar I, Yaramis A, Karaca E, Yis U, Sonmezler E, Ekinci B, et al. iScience. 2021 Jan 22; 24(1):101948. Epub 2020 Dec 30.
Bi-allelic Pathogenic Variants in TUBGCP2 Cause Microcephaly and Lissencephaly Spectrum Disorders. [Am J Hum Genet. 2019]
Bi-allelic Pathogenic Variants in TUBGCP2 Cause Microcephaly and Lissencephaly Spectrum Disorders.
Mitani T, Punetha J, Akalin I, Pehlivan D, Dawidziuk M, Coban Akdemir Z, Yilmaz S, Aslan E, Hunter JV, Hijazi H, et al. Am J Hum Genet. 2019 Nov 7; 105(5):1005-1015. Epub 2019 Oct 17.
The mammalian gamma-tubulin complex contains homologues of the yeast spindle pole body components spc97p and spc98p. [J Cell Biol. 1998]
The mammalian gamma-tubulin complex contains homologues of the yeast spindle pole body components spc97p and spc98p.
Murphy SM, Urbani L, Stearns T. J Cell Biol. 1998 May 4; 141(3):663-74.

RefSeq mRNA
See reference mRNA sequence for the TUBGCP2 gene (NM_001256618.2).
RefSeq protein isoforms
See 3 reference sequence protein isoforms for the TUBGCP2 gene.

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