Divergent human and mouse orthologs of a novel gene (WBSCR15/Wbscr15) reside within the genomic interval commonly deleted in Williams syndrome

Cytogenetics and Cell Genetics

Volumn 90, Issue 3-4, 2000, Pages 285-290

  Doyle, J L ^a   DeSilva, U ^a   Miller, W ^b   Green, Eric D ^a  

^a NATIONAL HUMAN GENOME RESEARCH INSTITUTE   (United States)

^b Pennsylvania State University   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACID; COMPLEMENTARY DNA; DNA;

AMINO ACID SEQUENCE; ANIMAL TISSUE; ARTICLE; CHROMOSOME 7Q; CHROMOSOME DELETION; GENE DELETION; GENE LOCATION; GENE MAPPING; GENE SEQUENCE; GENETIC CODE; GENETIC ORGANIZATION; GENOME; HUMAN; HUMAN TISSUE; MOUSE; NONHUMAN; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; PROTEIN EXPRESSION; WILLIAMS BEUREN SYNDROME;

ADAPTOR PROTEINS, SIGNAL TRANSDUCING; AMINO ACID SEQUENCE; ANIMALS; BASE SEQUENCE; CLONING, MOLECULAR; EXONS; EXPRESSED SEQUENCE TAGS; GENE EXPRESSION PROFILING; HUMANS; INTRONS; MICE; MOLECULAR SEQUENCE DATA; OPEN READING FRAMES; PHYSICAL CHROMOSOME MAPPING; PROTEINS; RNA SPLICE SITES; RNA, MESSENGER; SEQUENCE DELETION; SEQUENCE HOMOLOGY; WILLIAMS SYNDROME;

EID: 0034528516     PISSN: 03010171     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (30)

1. Basic local alignment search tool
2. Gapped BLAST and PSI-BLAST: A new generation of protein database search programs
3. The Pfam protein families database
4. Neuropsychological, neurological, and neuroanatomical profile of Williams syndrome
5. Prediction of complete gene structures in human genomic DNA
6. Williams syndrome
7. Comparative mapping of the region of human chromosome 7 deleted in Williams syndrome
8. Comparative genomic sequence analysis of the human and mouse cystic fibrosis transmembrane conductance regulator genes
9. Hemizygosity at the elastin locus in a developmental disorder, Williams syndrome
10. A computer program for aligning a cDNA sequence with a genomic DNA sequence
11. Genes for two autosomal recessive forms of chronic granulomatous disease assigned to 1q25 (NCF2) and 7q11.23 (NCF1)
12. Williams-Beuren syndrome: Genes and mechanisms
13. Rapid production of full-length cDNAs from rare transcripts: Amplification using a single gene-specific oligonucleotide primer
14. A p47-phox pseudogene carries the most common mutation causing p47-phox-deficient chronic granulomatous disease
15. Long human-mouse sequence alignments reveal novel regulatory elements: A reason to sequence the mouse genome
16. A complete physical contig and partial transcript map of the Williams syndrome critical region
17. The PROSITE database, its status in 1999
18. On the trail of genetic culprits in Williams syndrome
19. Evolutionary parameters of the transcribed mammalian genome: An analysis of 2,820 orthologous rodent and human sequences
20. Comparative analysis of 1196 orthologous mouse and human full-length mRNA and protein sequences
21. Natural history of Williams syndrome: Physical characteristics
22. PSORT: A program for detecting sorting signals in proteins and predicting their subcellular localization
23. Identification of genes from a 500-kb region at 7q11.23 that is commonly deleted in Williams syndrome patients
24. PMS2-related genes flank the rearrangement breakpoints associated with Williams syndrome and other diseases on human chromosome 7
25. Williams-Beuren syndrome: Unraveling the mysteries of a microdeletion disorder
26. A physical map, including a BAC/PAC clone contig, of the Williams-Beuren syndrome-deletion region at 7q11.23
27. The gene for replication factor C subunit 2 (RFC2) is within the 7q11.23 Williams syndrome deletion
28. A duplicated gene in the breakpoint regions of the 7q11.23 Williams-Beuren syndrome deletion encodes the initiator binding protein TFII-1 and BAP-135, a phosphorylation target of BTK
29. Using neural networks for prediction of the subcellular location of proteins
30. PipMaker - A web server for aligning two genomic DNA sequences