Citations for
1CNGB1, GRAP2, PRPH2, ROM1
The cGMP-gated channel and related glutamic acid-rich proteins interact with peripherin-2 at the rim region of rod photoreceptor disc membranes.
Poetsch A, Molday LL, Molday RS.
J Biol Chem 276(51):48009-16. Epub 2001 Oct 18. 2001
2PRPH2, ROM1
Rom-1 is required for rod photoreceptor viability and the regulation of disk morphogenesis.
Clarke G, Goldberg AF, Vidgen D, Collins L, Ploder L, Schwarz L, Molday LL, Rossant J, Szel A, Molday RS, Birch DG, McInnes RR.
Nat Genet 25(1):67-73. 2000
3PRPH2, ROM1
Disulfide-mediated oligomerization of Peripherin/Rds and Rom-1 in photoreceptor disk membranes. Implications for photoreceptor outer segment morphogenesis and degeneration.
Loewen CJ, Molday RS.
J Biol Chem 275(8):5370-8. 2000
4PRPH2, ROM1
Analysis of the rds/peripherin.rom1 complex in transgenic photoreceptors that express a chimeric protein.
Kedzierski W, Weng J, Travis GH.
J Biol Chem 274(41):29181-7. 1999
5ROM1
Putative association of a mutant ROM1 allele with retinitis pigmentosa.
Martinez-Mir A, Vilela C, Bayes M, Valverde D, Dain L, Beneyto M, Marco M, Baiget M, Grinberg D, Balcells S, Gonzalez-Duarte R, Vilageliu L.
Hum Genet 99(6):827-30. 1997
6PRPH2, ROM1, RP7
Dominant and digenic mutations in the peripherin/RDS and ROM1 genes in retinitis pigmentosa.
Dryja TP, Hahn LB, Kajiwara K, Berson EL.
Invest Ophthalmol Vis Sci 38(10):1972-82. 1997
7ROM1
Mutation analysis of the ROM1 gene in retinitis pigmentosa.
Bascom RA, Liu L, Heckenlively JR, Stone EM, McInnes RR.
Hum Mol Genet 4(10):1895-902. 1995
8ROM1
A heterozygous putative null mutation in ROM1 without a mutation in peripherin/RDS in a family with retinitis pigmentosa.
Sakuma H, et al.
Genomics 27 : 384-386. 1995
9ROM1, VMD4
A recombination event excludes the ROM1 locus from the best's vitelliform macular dystrophy region.
Stšhr H, et al.
Hum Genet 95 : 219-222. 1995
10ROM1, BEST1
Refining the locus for Best vitelliform macular dystrophy and mutation analysis of the candidate gene ROM1.
Nichols BE, Bascom R, Litt M, McInnes R, Sheffield VC, Stone EM.
Am J Hum Genet 54(1):95-103. 1994
11ROM1, PRPH2, RP7
Digenic retinitis pigmentosa due to mutations at the unlinked peripherin/RDS and ROM1 loci.
Kajiwara K, et al.
Science 264 : 1604-1608. 1994
12ROM1
Polymorphisms and rare sequence variants at the ROM1 locus.
Bascom RA, et al.
Hum Mol Genet 2 : 1975-1977. 1993
13ROM1
Cloning of the human and murine ROM1 genes : genomic organization and sequence conservation.
Bascom RA, et al.
Hum Mol Genet 2 : 385-391. 1993
14ROM1
ROM1 : a candidate gene for autosomal dominant retinitis pigmentosa (ADRP), Usher syndrome type 1, and Best vitelliform macular dystrophy.
Bascom RA, et al.
Am J Hum Genet 51 : A6. 1992
15ROM1
Localization of the photoreceptor gene ROMI to human chromosome 11 and mouse chromosome 19 : sublocalization to human 11q13 between PGA and PYGM.
Bascom RA, et al.
Am J Hum Genet 51 : 1028-1035. 1992
16ROM1
Identification of a new mammalian photoreceptor-specific gene family.
Bascom R, et al.
Am J Hum Genet 45 : A172. 1989