UPF0729 protein C18orf32 [Homo sapiens]

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C18orf32 loss-of-function is associated with a neurodevelopmental disorder with hypotonia and contractures. [Hum Genet. 2022]
C18orf32 loss-of-function is associated with a neurodevelopmental disorder with hypotonia and contractures.
Salian S, Guo XY, Murakami Y, Kinoshita T, Kaur P, Shukla A, Girisha KM, Fujita M, Campeau PM. Hum Genet. 2022 Aug; 141(8):1423-1429. Epub 2022 Feb 2.
Multiplexed kinase interactome profiling quantifies cellular network activity and plasticity. [Mol Cell. 2023]
Multiplexed kinase interactome profiling quantifies cellular network activity and plasticity.
Golkowski M, Lius A, Sapre T, Lau HT, Moreno T, Maly DJ, Ong SE. Mol Cell. 2023 Mar 2; 83(5):803-818.e8. Epub 2023 Feb 2.
A proximity-dependent biotinylation map of a human cell. [Nature. 2021]
A proximity-dependent biotinylation map of a human cell.
Go CD, Knight JDR, Rajasekharan A, Rathod B, Hesketh GG, Abe KT, Youn JY, Samavarchi-Tehrani P, Zhang H, Zhu LY, et al. Nature. 2021 Jul; 595(7865):120-124. Epub 2021 Jun 2.

RefSeq mRNA
See reference mRNA sequence for the C18orf32 gene (NM_001035005.4).
RefSeq protein isoforms
See the other reference sequence protein isoform for the C18orf32 gene (NP_001186275.1).

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GlyGen glycoinformatics resource [GlyGen glycoinformatics resou...]
GlyGen glycoinformatics resource
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OncoMX cancer biomarker resource
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reagents
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