| C6orf89 | |||||||||||||||||||||||||||||||||||||||||||||||||||
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| Identifiers | |||||||||||||||||||||||||||||||||||||||||||||||||||
| Aliases | C6orf89 , BRAP, chromosome 6 open reading frame 89, PS1TP5TP1 | ||||||||||||||||||||||||||||||||||||||||||||||||||
| External IDs | OMIM: 616642 MGI: 2136782 HomoloGene: 12728 GeneCards: C6orf89 | ||||||||||||||||||||||||||||||||||||||||||||||||||
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| Wikidata | |||||||||||||||||||||||||||||||||||||||||||||||||||
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Uncharacterized protein C6orf89 is a protein that in humans is encoded by the C6orf89 gene. [5]
Myotubularin-related protein 6 is a protein that in humans is encoded by the MTMR6 gene.
Synaptotagmin-3 is a protein that in humans is encoded by the SYT3 gene.
Ergosterol biosynthetic protein 28 is a protein that in humans is encoded by the ERG28 gene.
Beta-taxilin is a protein that in humans is encoded by the TXLNB gene.
Rho guanine nucleotide exchange factor (GEF) 3, also known as ARHGEF3, is a human gene.
TIMMDC1 is a protein that in humans is encoded by the TIMMDC1 gene. It is a chaperone protein involved in constructing the membrane arm of mitochondrial Complex I. A frameshift mutation in an intron of this gene has been shown to cause failure to thrive, retardation of psychomotor development, infantile-onset hypotonia, and severe neurologic dysfunction. High expression of this gene has been associated with migration of lung cancer cells while depletion of the protein has been shown to affect regulation of apoptosis, the cell cycle, and cell migration.
Neuronal-specific septin-3 is a protein that in humans is encoded by the SEPT3 gene.
LisH domain-containing protein ARMC9 is a protein that in humans is encoded by the ARMC9 gene.
Transmembrane protein 47 is a protein that in humans is encoded by the TMEM47 gene.
FCH domain only protein 2 is a protein that in humans is encoded by the FCHO2 gene.
High-mobility group protein B3 is a protein that in humans is encoded by the HMGB3 gene.
Synaptotagmin-13 is a protein that in humans is encoded by the SYT13 gene.
Spartan (SPRTN) is a protein that in humans is encoded by the SPRTN gene. It is involved in DNA repair. Ruijs-Aalfs syndrome is an autosomal recessive genetic disorder. Characteristics of this disorder are features of premature aging, chromosome instability and development of hepatocellular carcinoma. Ruijs-Aalfs syndrome arises as a result of mutations in the SPRTN gene that encodes a metalloproteinase employed in the repair of protein-linked DNA breaks.
Mitochondrial pyruvate carrier 2 (MPC2) also known as brain protein 44 (BRP44) is a protein that in humans is encoded by the MPC2 gene. It is part of the Mitochondrial Pyruvate Carrier (MPC) protein family. This protein is involved in transport of pyruvate across the inner membrane of mitochondria in preparation for the pyruvate dehydrogenase reaction.
Zinc finger protein 471 is a protein that in humans is encoded by the ZNF471 gene.
Zinc finger protein 34 is a protein that in humans is encoded by the ZNF34 gene.
Ankyrin repeat domain-containing protein 13C is a protein that in humans is encoded by the ANKRD13C gene.
SLIT and NTRK-like protein 6 is a protein that in humans is encoded by the SLITRK6 gene.
Leucine-rich repeat-containing protein 39 is a protein that in humans is encoded by the LRRC39 gene.
60S ribosomal protein L10-like is a protein that in humans is encoded by the RPL10L gene.
 | This article on a gene on human chromosome 6 is a stub. You can help Wikipedia by expanding it. |
