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1. Subscription: Automated Splice Site and Exon Definition Analysis Server
If your guest access to the ASSEDA server has been exhausted, you have been automatically directed here to the Cytognomix website. The server is described in our recent paper, “Prediction of Mutant mRNA Splice Isoforms by Information Theory-Based Exon Definition.” You may obtain an subscription through our secure Paypal account which provides unrestricted access to the site. The annual fee is $200 (plus applicable taxes), which entitles you to unrestricted use of the server for 365 days*. Please provide your account Email address below and payment information as requested. We will notify you by Email when the guest account has been converted to a subscription.
*ASSEDA and the backup server are generally available 24/7, however we cannot assure 100% uptime
2. Software: Shannon pipeline plug-in for mRNA splicing mutation analyis
This product is available either as a stand-alone workbench or remote server versions from our distributor, CLC bio.
Careers
Located in the London Ontario, Cytognomix Inc. offers employees rewarding and challenging careers in an exciting, evolving market. Quite simply, Cytognomix is a pioneer in the genomics and genome bioinformatics industry.
We welcome new employees with a pioneering spirit. Fresh ideas. Different perspectives. Creative minds.
Experience in software development, bioinformatics, genome-scale thinking are sought.
Cytognomix is growing in a variety of areas. Currently there are no open positions at Cytognomix.
Cytognomix receives new US Patent
US patent (8,209,129) was issued today on Single Copy DNA probes that include divergent repetitive sequences, thus extending the portions of the genome that can be used for such probes beyond traditional single copy sequences. The technology also increases the density of genomic DNA probes for higher resolution genetic analysis beyond what is used in FISH, genomic microarrays for array comparative genomic hybridization, and solution capture hybrdization arrays for sequence enrichment in deep sequencing. The patent has been licensed to Cytognomix.
Products
Shannon pipeline:
Genome-scale interpretation of mutations (Try it now!)
Software to predict splicing mutations along a chromosome
About Us
Cytognomix is a London, Ontario based biotechnology company developing software-based solutions and reagents for clinical genomics. The company has a significant intellectual property portfolio, which emphasizes products for clinical diagnostic applications. Current products include mutation interpretation software, DNA probe reagents and companion software to detect chromosome abnormalities at the molecular level.
Cytognomix’s proprietary Single Copy (sc) technology brings precise, sensitive, and informative genetic disease management tools to advanced clinical laboratories for detection of chromosome anomalies related to genetic disease. Cytognomix designs and produces molecular cytogenetic tests using fluorescent in-situ hybridization scFISH probes. In addition, microarray-based comparative genomic hybridization (aCGH) can use SC technology to increase reproducibility and reduce cost per sample. A key Cytognomix tool is our proprietary genome browser interface that simplifies selection of single copy probes for nearly any gene-mapped disease. Cytognomix’s scFISH probes will assure correct diagnosis and make possible more personalized treatment than conventional approaches.
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Subtelomeric SC-FISH probes Catalog(Continued)
|
|
Chr. Target
|
scFISH probes1
|
Competitor Recombinant probes2 | |||
| Catalog Number | Chr |
Length(bp) |
Distance from Telomere (kb)3
|
Estimated clone size |
Approx distance of STS from telomere (kb)4 | |
| ST-0000131 | 8ptel | 2271 | 455.377 – 457.645 | |||
| 2154 | 71.870 | - 74.023 | 100 kb6 | 194 ± 100 | ||
| ST-0000132 | 8qtel | |||||
| ST-0000133 | 8qtel | 2949 | 145.868 – 148.816 | |||
| ST-0000134 | 9ptel | 1754 | 243.057 – 244.809 | 115 kb | 140 ± 1159 | |
| ST-0000135 | 9qtel | 2232 | 248.993 – 251.226 | 95 kb | 223 ± 95 | |
| ST-0000136 | 9qtel | 2707 | 231.636 – 234.340 | |||
| ST-0000137 | 9qtel | 2278 | 257.634 – 259.785 | |||
| ST-0000138 | 10ptel | 2132^+ | 363.852 – 365.942 | 80 kb6 | 328 ± 80 | |
| ST-0000139 | 10ptel | 2051+ | 320.896 – 322.898 | |||
| ST-0000140 | 10ptel | 3203+ | 282.669 – 285.872 | |||
| ST-0000141 | 10ptel | 2526^+ | 151.566 – 154.092 | |||
| 1820 | 75 kb | 193 ± 75 | ||||
| ST-0000142 | 10qtel | 184.961 – 186.780 | ||||
| ST-0000143 | 11ptel | 2884 | 1,205.118 | - 1,208.002 | 110 kb6 | 290 ± 110 |
| 2489* | ||||||
| ST-0000144 | 11ptel | 66.589 – 69.078 | ||||
| 2462 | 1,781.588 | - 1,784.049 | 160 kb | unknown | ||
| ST-0000145 | 11qtel | |||||
| ST-0000146 | 11qtel | 2026* | 33.471 – 31.445 | |||
| 1914 | 100 kb | 0-209 | ||||
| ST-0000147 | 12ptel | 180.472 – 182.385 | ||||
| 3456 | 165 kb | 180 ± 165 | ||||
| ST-0000148 | 12qtel | 154.406 – 157.861 | ||||
| ST-0000149 | 13qtel | 3209 | 366.172 – 369.380 | 75 kb | 2,900 ± 75 | |
| ST-0000150 | 14qtel | 1866 | 3,155.170 | - 3,157.035 | 160 kb | (4,100-4,200) ± 117 |
| ST-0000151 | 14qtel | 3839 | 3,128.031 | - 3,131.869 | ||
| ST-0000152 | 14qtel | 1984* | 1,022.102 – 1,020.118 | |||
| ST-0000153 | 14qtel | 2617* | 1,019.175 – 1,016.558 | |||
| ST-0000154 | 15qtel | 1607 | 131.552 – 133.158 | 100kb | 420 ± 100 | |
| ST-0000155 | 16ptel | 3361* | 73.825 – 77.186 | 110 kb | 3056± 110 | |
| 2082* | ||||||
| ST-0000156 | 16ptel | 56.610 – 58.692 | ||||
| 2567 | 110 kb6 | 210 ± 110 | ||||
| ST-0000157 | 16qtel | 183.506 – 186.072 | ||||
| ST-0000158 | 17ptel | 2593 | 895.021 – 897.613 | 70 kb6 | 105 ± 70 | |
| ST-0000159 | 17ptel | 4984 | 859.347 – 864.330 | |||
| 2219* | ||||||
| ST-0000160 | 17ptel | 101.957 – 104.176 | ||||
| 6191* | ||||||
| ST-0000161 | 17qtel | 106.452 – 100.262 | ||||
| 3026 | 160 kb | 750 ± 160 | ||||
| ST-0000162 | 17qtel | 848.341 – 871.383 | ||||
| 2530 | 80.057 | 170 kb | (154-285) ± 40 | |||
| ST-0000163 | 18qtel | - 82.584 | ||||
| ST-0000164 | 19ptel | 1815 | 1,745.686 | - 1,747.500 | 80 kb | unknown |
| ST-0000165 | 19ptel | 2094 | 1,721.659 | - 1,723.752 | ||
| 2400* | ||||||
| ST-0000166 | 19ptel | 265.605 – 268.005 | ||||
| 4137* | ||||||
| ST-0000167 | 19ptel | 249.688 – 253.825 | ||||
| 2721 | 121.866 | 160 kb | 244 ± 160 | |||
| ST-0000168 | 19qtel | - 124.586 | ||||
| ST-0000169 | 19qtel | 2399 | 88.475 | - 90.874 | ||
| ST-0000170 | 20ptel | 2616 | 365.951 | - 368.566 | 160 kb | 0-240 |
| 3133 | 109.581 | 140 kb | 62-202 | |||
| ST-0000171 | 20qtel | - 112.713 | ||||
| ST-000172 | 20qtel | 3695 | 114.557 | - 118.251 | ||
| ST-0000173 | 20qtel | 2166 | 140.088 | - 142.253 | ||
| ST-0000174 | 20qtel | 2997 | 186.460 | - 189.456 | ||
| ST-0000175 | 21qtel | 4370 | 47.861 | - 52.230 | 170 kb | 0-337 |
| ST-0000176 | 22qtel | 3550 | 176.274 | - 178.618 | 80 kb | (161-168) ± 73 |
| ST-0000177 | Xptel | 1896 | 2,329.080 | - 2,330.975 | 175kb | 324 ± 175 (X,Y homology)8 |
| 3700* | ||||||
| ST-0000178 | Xptel | 155.557 – 159.257 | ||||
| 2529 | 645.399 | 170kb | 0-258 | |||
| ST-0000179 | Xqtel | - 647.927 | ||||
| ST-0000180 | Yptel | 2446 | 2,562.365 | - 2,564.810 | 175kb | Unknown (X,Y homology)8 |
| ST-0000181 | Yptel | 2000 | 2,567.816 | - 2,569.815 | 170kb |
Patent Information
Previous Page
1 scFISH probes developed from April 2003 genome draft are labeled with asterisk (*). The remaining probes were from April 01 draft except 1p (Nov 02), 2q, 3q, 4p, 5p, 6, 8q, 9p (June 02). Sequence IDs corresponding to these probes contain the UCSC database version number in the descriptions of these products.
2 Many of conventional FISH probes were developed by Knight et al. Am. J. Hum. Genet. 67: 320, 2000, and by Abbott Laboratories/Vysis, Inc.
3Distance from probe to end of the telomere reported in this table is based on the length of the interval from the probe boundary coordinates to the terminal nucleotide coordinates of each chromosome end in the April 03 version of genome sequence. The computer program BLAT at the Genome Browser website (genome.ucsc.edu) was used to determine these coordinates. Due to inaccuracy in the BLAT algorithm, the coordinates of probe boundaries may differ from the actual coordinates slightly.
4 The position of STS/ marker associated with the conventional FISH probe was determined in the April 03 version of the genome sequence. Often a single STS/ marker is identified on a clone. There is insufficient information available to determine the positions of STS markers on some of these clones. As a result, error in positioning a probe on the chromosome (ie. ± ) is generally the size of the clone provided in: American Journal of Human Genetics 67: p. 320, 2000, and by Abbott/Vysis, Inc . A standard deviation less than the estimated clone size indicates that more than one STS was localized to the clone.
6 Indicates clones with cross hybridizations to other chromosomes.
7 Probe recognizes a neighboring paralogous sequence in addition to the known interval.
8 Reported STS located on X chromosome only, but both commercial probes for sex chromosomes show homology with each other.
9 Probe detect four paralogs: three of which are on chromosome 9 and one which is on chromosome 2.
unknown = Reported STS/ markers could not be placed on genome sequence as they could not be located in all available genome databases or through communication with authors.
^hybridization was detected when probe was combined with other 10ptel probes labeled with “^”.
+ hybridization was detected when probe was combined with other 10ptel probes labeled with “+”.
Subtelomeric SC-FISH probes Catalog
|
|
Chr. Target
|
scFISH probes1
|
Competitor Recombinant probes2 | |||
| Catalog Number | Chr |
Length(bp) | Distance from Telomere (kb)3
|
Estimated clone size | Approx distance of STS from telomere (kb)4 | |
| ST-0000101 | 1ptel | 2531* | 1,045.411 – 1,047.942 | 90 kb | unknown | |
| 3930* | 1,048.515 – 1,052.445 | |||||
| ST-0000102 | 1ptel | |||||
| 3512* | 1,053.361 – 1,056.873 | |||||
| ST-0000103 | 1ptel | |||||
| 2671 | 3,858.025 | - 3,860.694 | ||||
| ST-0000104 | 1ptel | |||||
| 1853 | 7,939.921 | - 7,941.773 | 100 kb | 236 ± 100 | ||
| ST-0000105 | 1qtel | |||||
| ST-0000106 | 1qtel | 1632* | 97.847 – 96.215 | |||
| 2503 | 89.194-86.692 | |||||
| ST-0000107 | 1qtel | |||||
| 2653 | 175 kb | 322 ± 175 | ||||
| ST-0000108 | 2ptel | 112.585 – 115.237 | ||||
| 3355 | 2,398.933 | - 2,402.287 | 60 kb | 390 ± 46 | ||
| ST-0000109 | 2qtel | |||||
| ST-0000110 | 3ptel | 2093* | 181.265-183..325 | 80 kb | 248 ± 80 | |
| 1834* | 199.161-200..994 | |||||
| ST-0000111 | 3ptel | |||||
| 2953 | 762.774 | - 765.726 | 95 kb6 | 997 ± 95 | ||
| ST-0000112 | 3qtel | |||||
| 2022* | ||||||
| ST-0000113 | 3qtel | 595.753 – 593.731 | ||||
| ST-0000114 | 4ptel | 1796 | 246.384 – 248.179; 417.863 – 419.7107 | 145 kb6 | (220-292) ± 73 | |
| 2426 | 442.967 | - 445.387 | 130 kb | 930 ± 130 | ||
| ST-0000115 | 4qtel | |||||
| ST-0000116 | 5ptel | 2189 | 86.825 | - 89.013 | 191kb | unknown |
| 2795 | 2,032.602 | - 2,035.396 | 105 kb | 227 ± 105 | ||
| ST-0000117 | 5qtel | |||||
| ST-0000118 | 5qtel | 2661 | 2,019.454 | - 2,022.114 | ||
| ST-0000119 | 5qtel | 2633* | 627.290 – 624.657 | |||
| ST-0000120
|
5qtel | 1753* | 422.516 – 420.763 | |||
| ST-0000121 | 6ptel | 2152 | 199.487 | - 201.638 | 80 kb | unknown |
| 2554 | 175.551 | - 178.104 | 100 kb | (276-282) ± 94 | ||
| ST-0000122 | 6qtel | |||||
| ST-0000123 | 7ptel | 2872 | 815.565 | - 818.439 | 60 kb | 218 ± 59 |
| 2434* | ||||||
| ST-0000124 | 7ptel | 143.257 – 145.691 | ||||
| 2348* | ||||||
| ST-0000125 | 7ptel | 146.749 – 149.097 | ||||
| 2574 | 1,095.575 | - 1,098.148 | 95 kb | 225 ± 95 | ||
| ST-0000126 | 7qtel | |||||
| 1517* | ||||||
| ST-0000127 | 7qtel | 28.945 – 27.428 | ||||
| 1634* | ||||||
| ST-0000128 | 7qtel | 5.405 – 3.771 | ||||
| 1865* | ||||||
| ST-0000129 | 7qtel | 81.313 – 79.448 | ||||
| ST-0000130 | 8ptel | 2079 | 483.728 – 485.805 | 135 kb | 1,200 ± 135 |
Patent Information
Next Page
Read more >>
Standard Fish Probes Catalog (Continued)
| Chromosome /Disorder | Catalog Number | GenBank Accession | Gene | Interval | Cytogenetic nomenclature |
| 16/AML-M4 | ST-0000034 | NT_000691 | PM53 | ~20 kb downstream | ish inv(16)(p13q22)(PM5 sp) |
| (Acute Myelogenous leukemia – M4) | ST-0000035 | NT_000691 | PM53 | ~60 kb downstream | |
| ST-0000036 | NT_000691 | PLA2G103
PKD PM5 |
IVS 3
IVS 12-Exon 15 ~100 kb upstream |
ish inv(16)(p13q22)(PLA2G10 mv, PKD mv, PM5 sp) | |
| ST-0000037 | NT_000691 | PLA2G103
PKD PM5 |
IVS 3
Exon 15-IVS 20 ~100 kb upstream & ~300 kb downstream |
||
| ST-0000038 | NT_025903 | ABCC1/MDR1 | IVS 6 | ish inv (16)(p13q22)(ABCC1st) | |
| 16/Ruben- stein-Taybi Sx | ST-0000039 | NT_000671 | CREBBP | IVS 19 – IVS 20 | ish del(16)(p13.3)(CREBBP-) |
| ST-0000040 | NT_000671 | CREBBP | IVS 19 | ||
| 17/Smith- Magenis Sx | ST-0000041 | NT_000770 | ADORA2B4 | Promoter-IVS 1 | ish del (17)(p11.2p11.2)(ADORA2B-) |
| ST-0000042 | NT_000770 | ADORA2B4 | IVS 1 | ||
| ST-0000043 | U80184 | FLI1 | IVS 12-IVS 14 | ish del (17)(p11.2p11.2)(FLI1-) | |
| ST-0000044 | U80184 | FLI1 | IVS 15-Exon 21 | ||
| ST-0000045 | NT_000760 | MFAP4 | IVS 2 – 3 UTR | ish del(17)(p11.2p11.2)(MFAP4-) | |
| ST-0000046 | AL035367 | ZNF179-PAIP1;
LLGL/HUGL; SHMT1 |
Between ZNF179 PAIP1; IVS7-Exon 13; IVS 4 | ishdel (17)(p11.2p11.2) (ZNF179/PAIP1/SHMT1-) | |
| ST-0000047 | AL035367 | LLGL/HUGL | Promoter –Exon 1
Promoter – IVS1 |
ish del(17)(p11.2p11.2)(LGLL/HUGL-) | |
| 17/Charcot-
Marie–Tooth 1A |
ST-0000048 | AC005703 | PMP22 | Promoter
(~5 kb upstream) |
ish dup(17)(p11.2p11.2)( PMP22++) |
| ST-0000049 | AC005703 | PMP22 | IVS 3 | ||
| ST-0000050 | AC005703 | PMP224 | IVS 3 | ||
| 17/ Miller-Dieker Sx | ST-0000051 | NT_000774 | PAFAH1B1 | ~5kb downstream | ish del(17)(p13.3)(PAFAH1B1/EIF-3-)
|
| EIF-35 | IVS 24–IVS 27 | ||||
| ST-0000052 | NT_000774 | PAFAH1B1 | ~7-8 kb downstream | ||
| EIF-35
|
IVS 15-IVS 19 | ||||
| ST-0000053 | NT_000774 | PAFAH1B1 | ~13 kb downstream | ||
| ST-0000054 | EIF-35
|
IVS 5-IVS 11 | |||
| Alagille Sx | ST-0000055 | AL035456.24 | JAG1 | IVS 2-IVS 3 | ish del(20)(p12.3p12.3)(JAG1-) |
| ST-0000056 | AL035456.24 | JAG1 | IVS 5-IVS 8 | ||
| 21/Down Sx | ST-0000057 | AP000160 | DSCR4 | ~39 kb upstream | ish (21)(q22.2q22.3)(DSCR4x3) |
| ST-0000058 | AP000160 | DSCR4 | ~30 kb upstream | ||
| ST-0000059 | AP000160 | DSCR4 | ~20 kb upstream | ||
| 21/ ALL | ST-0000060 | AP000057 | AML1/RUNX | Promoter-exon 1 | ish t(12;21)(p13;q22)(AML1 st) |
| 22/ DiGeorge Sx | ST-0000061 | NT_001039 | HIRA | IVS 21-IVS 24 | ish del(22)(q11.2)(HIRA-) |
| ST-0000062 | NT_001039 | HIRA | IVS 13-IVS 15 | ||
| ST-0000063 | NT_001039 | HIRA | IVS 12-IVS 13 | ||
| ST-0000064 | NT_001039 | HIRA | IVS 2-IVS 4 | ||
| ST-0000065 | |||||
| 22/CML; ALL | ST-0000066 | U07000 | BCR | Proximal to major
breakpoint in CML |
ish t(9;22)(q34;q11.2)(BCR st) |
| ST-0000067 | U07000 | BCR | Proximal to major breakpoint in CML | ||
| ST-0000069 | U07000 | BCR | IVS 8 | ish t(9;22)(q34;q11.2)(BCR mv) | |
| X/ Kallman Sx | ST-0000070 | NT_ 001457 | GS2 | Promoter- IVS 2 | ish del(X)(p22.31)(GS2-) |
| ST-0000071 | AC006062 | KAL1 | IVS 6-IVS 7 | ish del(X)(p22.31)(KAL1-) | |
| ST-0000072 | AC006062 | KAL1 | ~8 kb downstream | ||
| X/ Turner; Leri- Weill Sx | ST-0000073 | NT_001151 | SHOX | IVS 2- exon 3 | ish del(X)(p22.33)(SHOX-) |
| ST-0000074 | NT_001151 | SHOX | IVS 4 | ||
| ST-0000075 | NT_001151 | SHOX | IVS 6 | ||
| ST-0000076 | NT_001159 | TBL1 | IVS 3 | ish del(X)(p22.22-22.31)(TBL1-) | |
| ST-0000077 | NT_001159 | TBL1 | Exon 15- 3 |
|
Standard Fish Probes Catalog
Table 1. scFISH probes used to detect cytogenetic abnormalities
| Chromosome /Disorder | Catalog Number | GenBank Accession | Gene | Interval** | Cytogenetic nomenclature |
| 1/Monosomy 1p36 Sx | ST-0000001 | AL031282 | CDC2L1 | IVS 11-3 UTR | ish del (1)(p36.3)(CDC2L1-) |
| ST-0000002 | AL031282 | CDC2L1 | 3 UTR | ||
| 4/ Wolf-Hirschorn Sx | ST-0000003 | NT_000102 | HD | Exon 67 – 0.2 kb downstream | ish del (4)(p16.3)(HD-) |
| 5/Cri-du-Chat Sx | ST-0000004 | NT_000149 | CTNND2 | IVS 17 | ish del (5)(p15.2)(CTNND2-) |
| ST-0000005 | NT_000149 | CTNND2 | IVS 14 | ||
| ST-0000006 | NT_000149 | CTNND2 | IVS 13 | ||
| ST-0000007 | NT_000147 | SEMA5A | IVS 3 | ish del (5)(p15.31)(SEMA5A-) | |
| ST-0000008 | NT_000147 | SEMA5A | IVS 3 | ||
| ST-0000009 | NT_000147 | SEMA5A | IVS 3 | ||
| ST-0000010 | AF119117 | SLC6A3 | IVS 3 | ish del (5)(p15.33)(SLC6A3-) | |
| 7/Williams Sx | ST-0000011 | NT_000398 | L1MK1 | IVS 2 | ish del(7)(q11.23q11.23)(LIMK1-) |
| ST-0000012 | NT_000398 | L1MK1 | IVS 13-3UTR | ||
| 8/Langer- | ST-0000013 | NT_002886 | TRPS1 | IVS 1 | ish del(8)(q23.3q24.1)(TRPS1-) |
| Giedeon Sx | ST-0000014 | NT_002886 | TRPS1 | IVS 1 | |
| 9/CML | ST-0000015 | U07561 | ABL1 | Exon 1b-IVS 1b | ish t(9;22)(q34;q11.2)(ABL st) |
| (Chronic myelogenous leukemia) | ST-0000016 | U07562 | ABL1 | IVS 1b | |
| ST-0000017 | U07563 | ABL1 | IVS 3 | ish t(9;22)(q34;q11.2)(ABL mv) | |
| ST-0000018 | U07563 | ABL1 | IVS 3 | ||
| ST-0000019 | U07563 | ABL1 | IVS 4-IVS 6 | ish t(9;22)(q34;q11.2)(ABL mv) | |
| ST-0000020 | U07563 | ABL1 | Exon 11-IVS 11 | ||
| 12/ALL (Acute lymphocytic leukemia) | ST-0000021 | NT_000601 | TEL/ETV6 | IVS2 | ish t(12;21)(p13;q22)(TEL sp) |
| ST-0000022 | NT_000601 | TEL/ETV6 | IVS3 | ||
| ST-0000023 | NT_000601 | TEL/ETV6 | IVS5-IVS6 | ||
| 13/ Aneuploidy | ST-0000024 | AL355338 | ZIC2 | ~5.8 kb downstream | ish del(13)(q32)(ZIC2-) or |
| ST-0000025 | AL355338 | ZIC2 | ~2 kb upstream | ish del(13)(q32)(ZIC2x3) | |
| 15/Prader-Willi, Angelman & Duplication Sx | ST-0000026 | AC004600 | UBE3A | IVS 8-IVS 9 | ish del(15)(q11.2q11.2)(UBE3A-) |
| ST-0000027 | AC004737 | IC/SNRPN | IVS 3 to Exon u1B2 | ish del(15)(q11.2q11.2)(IC/ SNRPN-) | |
| ST-0000028 | U41384.1 | SNRPN | Promoter – IVS 1 | ish dup(15)(q11.2q13)(UBE3A++, | |
| ST-0000029 | AC004737 | IC/SNRPN | IVS 5-Exon u1B2-IVS 3 | IC/SNRPN++), and ish dic(15q11.2q13) (UBE3A++,IC/SNRPN++) | |
| ST-0000030 | AC004737 | IC/SNRPN | IVS 5-Exon u1B | ||
| ST-0000031 | AC006596 | MAGEL2 | CDS- 3 UTR-2 kb downstream | ish del(15)(q11.1q11.2)(MAGEL2-) or | |
| ST-0000032 | AC006596 | MAGEL2 | ~4 kb downstream | ish dup (15)(q11.2q11.2)(MAGEL2++) | |
| ST-0000033 | AC006596 | MAGEL2 | ~22 kb downstream |
Next Page
** WWW hyperlinks are to localized probe sequence in ContigView browser (v9.30a.1; 2 December 2002) at http://www.ensembl.org/Homo_sapiens/