thyroid hormone receptor-associated protein complex 240 kDa component- - Protein

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Molecular and Functional Characterisation of a Novel Intragenic 12q24.21 Deletion Resulting in MED13L Haploinsufficiency Syndrome. [Medicina (Kaunas). 2023]
Molecular and Functional Characterisation of a Novel Intragenic 12q24.21 Deletion Resulting in MED13L Haploinsufficiency Syndrome.
Siavrienė E, Petraitytė G, Mikštienė V, Maldžienė Ž, Sasnauskienė A, Žitkutė V, Ambrozaitytė L, Rančelis T, Utkus A, Kučinskas V, et al. Medicina (Kaunas). 2023 Jun 29; 59(7). Epub 2023 Jun 29.
The MED13L haploinsufficiency syndrome associated with de novo nonsense variant (P.GLN1981*). [J Mother Child. 2021]
The MED13L haploinsufficiency syndrome associated with de novo nonsense variant (P.GLN1981*).
Dawidziuk M, Kutkowska-Kaźmierczak A, Gawliński P, Wiszniewski W, Gos M, Stawiński P, Rydzanicz M, Kosińska J, Własienko P, Malinowska Kordowska O, et al. J Mother Child. 2021 Apr 30; 24(3):32-36. Epub 2021 Apr 30.
MED13L integrates Mediator-regulated epigenetic control into lung cancer radiosensitivity. [Theranostics. 2020]
MED13L integrates Mediator-regulated epigenetic control into lung cancer radiosensitivity.
Zhang N, Song Y, Xu Y, Liu J, Shen Y, Zhou L, Yu J, Yang M. Theranostics. 2020; 10(20):9378-9394. Epub 2020 Jul 23.

RefSeq genomic sequence
See the genomic reference sequence for the MED13L gene (NG_023366.1).
RefSeq protein isoforms
See 15 reference sequence protein isoforms for the MED13L gene.

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