RecName: Full=TBC1 domain family member 20

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Martsolf syndrome with novel mutation in the TBC1D20 gene in a family from Iran. [Am J Med Genet A. 2020]
Martsolf syndrome with novel mutation in the TBC1D20 gene in a family from Iran.
Hozhabri H, Talebi M, Mehrjardi MYV, De Luca A, Dehghani M. Am J Med Genet A. 2020 May; 182(5):957-961. Epub 2020 Mar 12.
Catalytic mechanism of a mammalian Rab·RabGAP complex in atomic detail. [Proc Natl Acad Sci U S A. 2012]
Catalytic mechanism of a mammalian Rab·RabGAP complex in atomic detail.
Gavriljuk K, Gazdag EM, Itzen A, Kötting C, Goody RS, Gerwert K. Proc Natl Acad Sci U S A. 2012 Dec 26; 109(52):21348-53. Epub 2012 Dec 12.
TBC1D20 is a Rab1 GTPase-activating protein that mediates hepatitis C virus replication. [J Biol Chem. 2007]
TBC1D20 is a Rab1 GTPase-activating protein that mediates hepatitis C virus replication.
Sklan EH, Serrano RL, Einav S, Pfeffer SR, Lambright DG, Glenn JS. J Biol Chem. 2007 Dec 14; 282(50):36354-61. Epub 2007 Sep 27.

RefSeq genomic sequence
See the genomic reference sequence for the TBC1D20 gene (NG_034082.1).
RefSeq protein
See the reference protein sequence for TBC1 domain family member 20 (NP_653229.1).

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Q96BZ9 [Domain Mapping of Disease Mut...]
Q96BZ9
Domain Mapping of Disease Mutations
MODBASE, Database of Comparative Protein Structure Models (Sali Lab/UCSF) [MODBASE, Database of Comparat...]
MODBASE, Database of Comparative Protein Structure Models (Sali Lab/UCSF)
Transcript/Protein Information [PANTHER Classification System]
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RecName: Full=TBC1 domain family member 20
RecName: Full=TBC1 domain family member 20
gi|34395569|sp|Q96BZ9.1|TBC20_HUMAN

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