Pikachurin
From Proteopedia
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| - | == | + | ==PIKACHURIN GENE== 0 |
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This is a default text for your page '''Pikachurin'''. Click above on '''edit this page''' to modify. Be careful with the < and > signs. | This is a default text for your page '''Pikachurin'''. Click above on '''edit this page''' to modify. Be careful with the < and > signs. | ||
| - | You may include any references to papers as in: | + | You may include any references to papers as in: Hu H, Li J, Zhang Z, Yu M (February 2011). "Pikachurin interaction with dystroglycan is diminished by defective O-mannosyl glycosylation in congenital muscular dystrophy models and rescued by LARGE overexpression". Neurosci. Lett. 489 (1): 10–5. |
| + | http://www.uniprot.org/uniprot/Q63HQ2. | ||
== Function ==Has a Dual function of photoreceptor visual synapse formation and visual perception | == Function ==Has a Dual function of photoreceptor visual synapse formation and visual perception | ||
| - | == Disease ==Visual Impairments were seen in mice with deleted pikachurin gene. | + | == Disease ==Visual Impairments were seen in mice with deleted pikachurin gene. Congenital muscular dystrophies (CMD) such as muscle-eye-brain disease caused by defective glycosylation of α-dystroglycan (α-DG) exhibit defective photoreceptor synaptic function. |
== Relevance == | == Relevance == | ||
Revision as of 21:44, 7 October 2016
==PIKACHURIN GENE== 0
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