The gene TSGA14, adjacent to the imprinted gene MEST, escapes genomic imprinting

Gene

Volumn 288, Issue 1-2, 2002, Pages 57-63

  Yamada, Takahiro ^a,b   Kayashima, Tomohiko ^a   Yamasaki, Kentaro ^a   Ohta, Tohru ^a   Yoshiura, Koh Ichiro ^a   Matsumoto, Naomichi ^a   Fujimoto, Seiichiro ^b   Niikawa, Norio ^a   Kishino, Tatsuya ^a  

^a NAGASAKI UNIVERSITY   (Japan)

^b HOKKAIDO UNIVERSITY   (Japan)

Author keywords

7q32; Imprinted domain; MEST; TSGA14; Two alternatively spliced transcripts

Indexed keywords

AMINO ACID; PROTEIN; PROTEIN A14; UNCLASSIFIED DRUG;

ALLELE; ARTICLE; BRAIN; CONTROLLED STUDY; COPG2IT1 GENE; EXON; FETUS; FETUS (ANATOMY); GENE; GENOME IMPRINTING; HUMAN; HUMAN TISSUE; LIVER; MEST GENE; METHYLATION; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; TESTIS; TSGA14 GENE;

ALLELES; BASE SEQUENCE; CHROMOSOME MAPPING; CPG ISLANDS; DNA METHYLATION; FEMALE; GENE EXPRESSION; GENE ORDER; GENES; GENOMIC IMPRINTING; HUMANS; MALE; MOLECULAR SEQUENCE DATA; PROTEINS; TRANSCRIPTION, GENETIC;

EID: 0037123358     PISSN: 03781119     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0378-1119(02)00428-6     Document Type: Article

References (10)

1. Construction of physical and transcript map in the putative 7q32 imprinted region flanking MEST/PEG1
2. Human PEG1/MEST, an imprinted gene on chromosome 7
3. Identification of novel imprinted transcripts in the Prader-Willi syndrome and Angelman syndrome deletion region: Further evidence for regional imprinting control
4. A catalogue of imprinted genes and parent-of-origin effects in humans and animals
5. Imprinting in clusters: Lessons from Beckwith-Wiedemann syndrome
6. Maternal-specific methylation of the human IGF2R gene is not accompanied by allele-specific transcription
7. Characterization of the C3 YAC contig from proximal mouse chromosome 17 and analysis of allelic expression of genes flanking the imprinted Igf2r gene
8. Deletions of a differentially methylated CpG island at the SNRPN gene define a putative imprinting control region
9. Mapping of eight testis-specific genes to mouse chromosomes
10. The novel gene, γ2-COP (COPG2), in the 7q32 imprinted domain escapes genomic imprinting