Recent update from: 04.06.2000
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Description
PROML1 is a protein involved either in the generation of plasma membrane evaginations or in membrane remodelling on formation of a disk rim and closed disks of rod photoreceptors. Exons: 23
Markers / RFLPs:
D4S1602
Transcripts:
Regulatory elements:
Primers: Mutated exon |
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| Assignment: 4p16 | Involvement in Retinal Degenerations:
click here to see a compilation of
several Mutations found to underlie |
| Subunits: 1 | Amino acids:
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| Modifications: | Mr/ Weight:
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| Cofactors:
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Click on entry to see database record online
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| Protein | Subtype | Locus | Species | EC-No. | Swissprot | PIR | Prosite |
Click on entry to see database record online
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| Gene | Subtype | Locus | Species | Genbank | Unigene | Medline |
Click on entry to see database record online
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| Gene | Subtype | Locus | Species | Genome Database | Mouse Genome Database | OMIM | Locus Link |
1. Maw, M.A., Corbeil, D., Koch, J., Hellwig, A., Wilson-Wheeler, J.C., Bridges, R.J., Kumaramanickavel, G., John, S., Nancarrow, D., Röper, K., Weigmann, A., Huttner, W.B., and Denton, M.J. A frameshift mutation in prominin (mouse)-like 1 causes human retinal degeneration. 2000; Hum.Mol.Genet. 9: 27 - 34.
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Contact the editor: irpamp@irpa.org |
This site is maintained and edited by
Dr. rer. medic. Markus Preising, Dipl.Biol. Molecular Genetics Laboratory Department of Paediatric Ophthalmology, Strabismology and Ophthalmogenetics University of Regensburg Head: Prof. Dr. med. Birgit Lorenz |
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