The protein encoded by this gene is a member of the four-transmembrane L6 superfamily. Members of this family function in various cellular processes including cell proliferation, motility, and adhesion via their interactions with integrins. In human brain tissue, this gene is expressed at high levels in the parietal lobe, occipital lobe, hippocampus, pons, white matter, corpus callosum, and cerebellum. Knockout of the homologous gene in mouse results in a neurobehavioral phenotype with suggested enhanced motor coordination. A deletion mutation in the human gene is associated with specific language impairment-5. [provided by RefSeq, Jul 2016]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| TM4SF20-20-RE | 20 (40 μL) | 200 μL |  |
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| TM4SF20-20-OR | 20 (40 μL) | 200 μL |  |
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| TM4SF20-20-GO | 20 (40 μL) | 200 μL |  |
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| TM4SF20-20-GR | 20 (40 μL) | 200 μL |  |
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| TM4SF20-20-AQ | 20 (40 μL) | 200 μL |  |
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The protein encoded by this gene is a member of the four-transmembrane L6 superfamily. Members of this family function in various cellular processes including cell proliferation, motility, and adhesion via their interactions with integrins. In human brain tissue, this gene is expressed at high levels in the parietal lobe, occipital lobe, hippocampus, pons, white matter, corpus callosum, and cerebellum. Knockout of the homologous gene in mouse results in a neurobehavioral phenotype with suggested enhanced motor coordination. A deletion mutation in the human gene is associated with specific language impairment-5. [provided by RefSeq, Jul 2016]
Gene Symbol : TM4SF20
Gene Name : Transmembrane 4 L six family member 20
Chromosome : CHR 2: 227,379,305-227,362,040
Locus : 2q36.3
Alt. Genes : ABI2
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