RecName: Full=Trafficking kinesin-binding protein 1; AltName: Full=106 - Protein

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Expanding the phenotype of TRAK1 mutations: hyperekplexia and refractory status epilepticus. [Brain. 2018]
Expanding the phenotype of TRAK1 mutations: hyperekplexia and refractory status epilepticus.
Sagie S, Lerman-Sagie T, Maljevic S, Yosovich K, Detert K, Chung SK, Rees MI, Lerche H, Lev D. Brain. 2018 Jul 1; 141(7):e55.
Deleterious variants in TRAK1 disrupt mitochondrial movement and cause fatal encephalopathy. [Brain. 2017]
Deleterious variants in TRAK1 disrupt mitochondrial movement and cause fatal encephalopathy.
Barel O, Malicdan MCV, Ben-Zeev B, Kandel J, Pri-Chen H, Stephen J, Castro IG, Metz J, Atawa O, Moshkovitz S, et al. Brain. 2017 Mar 1; 140(3):568-581.
Elevated expression of MGb2-Ag/TRAK1 is correlated with poor prognosis in patients with colorectal cancer. [Int J Colorectal Dis. 2011]
Elevated expression of MGb2-Ag/TRAK1 is correlated with poor prognosis in patients with colorectal cancer.
An Y, Zhou Y, Ren G, Tian Q, Lu Y, Li H, Li K, Su T, Xu B, Chen S, et al. Int J Colorectal Dis. 2011 Nov; 26(11):1397-404. Epub 2011 May 15.

RefSeq protein isoforms
See 54 reference sequence protein isoforms for the TRAK1 gene.

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Q9UPV9 [Domain Mapping of Disease Mut...]
Q9UPV9
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]
Transcript/Protein Information
PANTHER Classification System
Reactome [Reactome]
Reactome
reagents [ExactAntigen/Labome]
reagents
ExactAntigen/Labome

RecName: Full=Trafficking kinesin-binding protein 1; AltName: Full=106 kDa O-Glc...
RecName: Full=Trafficking kinesin-binding protein 1; AltName: Full=106 kDa O-GlcNAc transferase-interacting protein; AltName: Full=Protein Milton
gi|13124654|sp|Q9UPV9.1|TRAK1_HUMAN

Protein
Lemur-(6-4)PP-rep1
Lemur-(6-4)PP-rep1

GEO DataSets
Campomelic Dysplasia
Campomelic Dysplasia
A congenital disorder of CHONDROGENESIS and OSTEOGENESIS characterized by hypoplasia of endochondral bones. In most cases there is a curvature of the long bones especially the...<br/>Year introduced: 2009

MeSH
Crystal Arthropathies
Crystal Arthropathies
Joint disorders that are characterized by accumulation of microcrystals in and around the joint including in the SYNOVIAL FLUID. They are classified according to the chemical ...<br/>Year introduced: 2017

MeSH

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Protein