TRIOBP | |||||||||||||||||||||||||||||||||||||||||||||||||||
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Identifiers | |||||||||||||||||||||||||||||||||||||||||||||||||||
Aliases | TRIOBP , DFNB28, TAP68, TARA, dJ37E16.4, HRIHFB2122, TRIO and F-actin binding protein | ||||||||||||||||||||||||||||||||||||||||||||||||||
External IDs | OMIM: 609761 MGI: 1349410 HomoloGene: 5104 GeneCards: TRIOBP | ||||||||||||||||||||||||||||||||||||||||||||||||||
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Wikidata | |||||||||||||||||||||||||||||||||||||||||||||||||||
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This article may be too technical for most readers to understand.(September 2018) |
TRIO and F-actin-binding protein is a protein that in humans is encoded by the TRIOBP gene. [5] [6] [7] [8]
This gene encodes a protein that interacts with Trio, which is involved with neural tissue development and in controlling actin cytoskeleton organization, cell motility, and cell growth. This trio-binding protein also associates with F-actin and stabilizes F-actin structures. Domains contained in this encoded protein are an N-terminal pleckstrin homology domain and a C-terminal coiled-coil region. Mutations in this gene have been associated with a form of autosomal-recessive nonsyndromic deafness. Multiple alternatively-spliced transcript variants that would encode different isoforms have been found for this gene, though some transcripts may be subject to nonsense-mediated decay (NMD). [8]
Usher syndrome type-1G protein is a protein that in humans is encoded by the USH1G gene.
Transmembrane protease, serine 3 is an enzyme that in humans is encoded by the TMPRSS3 gene.
Dynamin-3 is a protein that in humans is encoded by the DNM3 gene. The protein encoded by this gene is a member of the dynamin family which possess mechanochemical properties involved in actin-membrane processes, predominantly in membrane budding. DNM3 is upregulated in Sézary's syndrome.
Claudin-14 is a protein that in humans is encoded by the CLDN14 gene. It belongs to a related family of proteins called claudins.
ADP-ribosylation factor-like protein 6 is a protein that in humans is encoded by the ARL6 gene.
Myosin-XVIIIa is a protein that in humans is encoded by the MYO18A gene.
HCLS1-associated protein X-1 is a protein that in humans is encoded by the HAX1 gene.
Coronin-1C is a protein that in humans is encoded by the CORO1C gene.
NADH dehydrogenase [ubiquinone] flavoprotein 3, mitochondrial is an enzyme that in humans is encoded by the NDUFV3 gene.
Protein SGT1 is a protein that in humans is encoded by the ECD gene.
Actin-binding Rho-activating protein is a protein that in humans is encoded by the ABRA gene. The mouse and rat homologues are known as STARS and MS1 respectively.
WAS/WASL-interacting protein family member 2 is a protein that in humans is encoded by the WIPF2 gene.
Transmembrane channel-like protein 2 is a protein that in humans is encoded by the TMC2 gene.
Zinc finger protein 346 is a protein that in humans is encoded by the ZNF346 gene.
Cell migration-inducing and hyaluronan-binding protein (CEMIP), formerly known as KIAA1199, is a protein that in humans is encoded by the CEMIP gene. CEMIP has been shown to bind hyaluronic acid and catalyze its depolymerization independently of CD44 and hyaluronidases. Such function has been also been validated in mice.
MARVEL domain-containing protein 2 is a protein that in humans is encoded by the MARVELD2 gene.
Myosin-XV is a protein that in humans is encoded by the MYO15A gene.
Tropomodulin 2 (neuronal) also known as TMOD2 is a protein which in humans is encoded by the TMOD2 gene.
Cofilin 2 (muscle) also known as CFL2 is a protein which in humans is encoded by the CFL2 gene.
Espin, also known as autosomal recessive deafness type 36 protein or ectoplasmic specialization protein, is a protein that in humans is encoded by the ESPN gene. Espin is a microfilament binding protein.