Retina International's Scientific Newsletter - Serum Retinol-binding Protein

	Retina International's Scientific Newsletter
Editor's Notes from literature on Serum Retinol-binding Protein (SRBP, RBP4)

Recent update from: 06.02.2000

RBP4

Notes

Flanking markers: D10S571-D10S185
Binds transthyretin when loaded with Ry
Mutations cause fundus xerophthalmicus

Species: Homo sapiens

See also:

Chromosomal localisation	in man: 10q24
	in mouse:

Gene Data

Exons:

Primers:

Protein Data

Aminoacids:

Molecularweight	on SDS-PAGE:
	calculated:

Reference: (1)

References:

1. Seeliger, M.W., Biesalski, H.K., Wissinger, B., Gollnick, H., Gielen, S., Frank, J., Beck, S., and Zrenner, E. Phenotype in retinol deficiency due to a hereditary defect in retinol binding protein synthesis. 1999; Invest.Ophthalmol.Vis.Sci. 40: 3 - 11.
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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