1 | MAGEL2, MKRN3, NDN, PWS
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| A paternal deletion of MKRN3, MAGEL2 and NDN does not result in Prader-Willi syndrome.
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| Kanber D, Giltay J, Wieczorek D, Zogel C, Hochstenbach R, Caliebe A, Kuechler A, Horsthemke B, Buiting K.
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| Eur J Hum Genet 17(5):582-90. Epub 2008 Dec 10.
2009
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2 | MKRN1, MKRN2, MKRN3, MKRNP5, MKRNP6
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| The ancient source of a distinct gene family encoding proteins featuring RING and C(3)H zinc-finger motifs with abundant expression in developing brain and nervous system.
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| Gray TA, Hernandez L, Carey AH, Schaldach MA, Smithwick MJ, Rus K, Marshall Graves JA, Stewart CL, Nicholls RD.
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| Genomics 66(1):76-86. 2000
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3 | PWS, MKRN3, MKRN3AS
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| A novel imprinted gene, encoding a RING zinc-finger protein, and overlapping antisense transcript in the prader-willi syndrome critical region.
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| Jong MT, et al.
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| Hum Mol Genet 8(5):783-93. 1999
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4 | IC15, MKRN3, PWS, SNRPN, SNURF
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| Conserved characteristics of heterochromatin-forming DNA at the 15q11-q13 imprinting center.
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| Greally JM, Gray TA, Gabriel JM, Song L, Zemel S, Nicholls RD.
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| Proc Natl Acad Sci U S A 96(25):14430-5 1999
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5 | BRCA1, MKRN1, MKRN2, MKRN3, MKRNP1, MKRNP2, MKRNP3, MKRNP4, MKRNP5, MKRNP6, RNF139, SIAH1, SIAH2
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| RING fingers mediate ubiquitin-conjugating enzyme (E2)-dependent ubiquitination.
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| Lorick KL, Jensen JP, Fang S, Ong AM, Hatakeyama S, Weissman AM.
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| Proc Natl Acad Sci U S A 96(20):11364-9 1999
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6 | AS, D15F375S1, D15F376S1, DEXI, GABRA5, HERC2P1, HERC2P2, HERC2P3, MKRN3, PWS, UBE3A
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| Integrated YAC contig map of the Prader-Willi/Angelman region on chromosome 15q11-q13 with average STS spacing of 35 kb.
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| Christian SL, Bhatt NK, Martin SA, Sutcliffe JS, Kubota T, Huang B, Mutirangura A, Chinault AC, Beaudet AL, Ledbetter DH.
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| Genome Res 8(2):146-57. 1998
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7 | AS, IC15, IPW, PWS, MKRN3
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| Minimal definition of the imprinting center and fixation of a chromosome 15q11-q13 epigenotype by imprinting mutations.
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| Saitoh S, et al.
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| Proc Natl Acad Sci U S A 93 : 7811-7815. 1996
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8 | MKRN3
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| The ZNF127 gene encodes a novel C3HC4 zinc-finger protein and its expression is regulated by genomic imprinting.
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| Jong MTC, et al.
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| Am J Hum Genet 53 : 697. 1993
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9 | MKRN3
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| A BsaBI RFLP detected for probe pML34 (D15S9) on chromosome 15q.
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| Hamabe J, et al.
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| Nucleic Acids Res 19 : 4789. 1991
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10 | MKRN3, D15S10, D15S11, D15S12, D15S13, D15S14, D15S15, D15S16, D15S17, D15S18
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| Mapping, characterization, and diagnostic utilization of 10 DNA segments from the proximal long arm of human chromosome 15.
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| Latt SA, et al.
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| (HGM9) Cytogenet Cell Genet 46 : 644. 1987
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11 | PWS, MKRN3, D15S10, D15S14, D15S15, D15S16, D15S17, D15Z2
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| Isolation of molecular probes associated with the chromosome 15 instability in the Prader-Willy syndrome.
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| Donlon TA, et al.
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| Proc Natl Acad Sci U S A 83 : 4408-4412. 1986
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