FR306562
- Summary
- Sequence
| Summary | |
|---|---|
| ID | FR306562 |
| Description | |
| Accession | XR_000167 |
| Sequence Ontology | mature_transcript |
| Organism | |
| Genome Mapping | |
| human(hg18) 1 region | chr14:100365415-100397061(+)  |
| Cross Reference | |
| Gene Association / Sense Overlap / 5'UTR | |
| human(hg18) | CR593817 (uc001yif.1 ), hCG_25025 (uc001yid.1 ) |
| Gene Association / Sense Overlap / Exon | |
| human(hg18) | CR593817 (uc001yif.1 ), hCG_25025 (uc001yid.1 ) |
| Gene Association / Sense Overlap / Intron | |
| human(hg18) | FP504 (uc001yhv.2 , uc001yhw.2 , uc001yhx.2 , uc001yhy.2 , uc001yhz.2 , uc001yia.2 , uc001yib.2 , uc001yic.2 , uc001yie.2 , uc010avz.1 ), hCG_25025 (uc001yid.1 ) |
| Gene Association / Sense Overlap / 3'UTR | |
| human(hg18) | CR593817 (uc001yif.1 ), FP504 (uc001yhv.2 , uc001yhw.2 , uc001yhx.2 , uc001yhy.2 , uc001yhz.2 , uc001yia.2 , uc001yib.2 , uc001yic.2 , uc001yie.2 , uc010avz.1 ), hCG_25025 (uc001yid.1 ) |
| Sequence Similarity | |
| MicroArray / Affymetrix GeneChip Exon Array / hg18 | ||
|---|---|---|
| Probe | Transcript Cluster | Probe Locus |
| 5917516 | 3552103 |
chr14:100365537-100365561(+) |
| 5004089 | 3552103 |
chr14:100365621-100365645(+) |
| 682943 | 3552103 |
chr14:100366047-100366071(+) |
| 6264247 | 3552103 |
chr14:100366070-100366094(+) |
| 5145422 | 3552103 |
chr14:100366491-100366515(+) |
| 4592485 | 3552103 |
chr14:100366842-100366866(+) |
| MicroArray / Invitrogen Ncode Noncoding RNA Array / hg18 | ||
|---|---|---|
| Probe | Target Transcript | Probe Locus |
| IVGNh22236 | CR610233 |
chr14:100366645-100366705(+) |
| Reference | |
|---|---|
|
RNAdb--a comprehensive mammalian noncoding RNA database.
Pang KC.,Stephen S.,Engström PG.,Tajul-Arifin K.,Chen W.,Wahlestedt C.,Lenhard B.,Hayashizaki Y. and Mattick JS. Nucleic Acids Res 33 (Database issue), D125-30 (2005)
Novel imprinted DLK1/GTL2 domain on human chromosome 14 contains motifs that mimic those implicated in IGF2/H19 regulation.
Wylie AA.,Murphy SK.,Orton TC. and Jirtle RL. Genome Res 10 (11), 1711-8 (2000)
Identification of an imprinted gene, Meg3/Gtl2 and its human homologue MEG3, first mapped on mouse distal chromosome 12 and human chromosome 14q.
Miyoshi N.,Wagatsuma H.,Wakana S.,Shiroishi T.,Nomura M.,Aisaka K.,Kohda T.,Surani MA.,Kaneko-Ishino T. and Ishino F. Genes Cells 5 (3), 211-20 (2000) | |
