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