Adams et al. (1993). GenBank, EST Data base. Accession No.: 659423. Publically available Aug. 19, 1993. (Also has ESTO1442 No.). |
GenBank.RTM. Accession No. D90162 for, "Human DNA from chromosome 8 containing translocation breakpoint" Sep., 1990. |
GenBank.RTM. Accession No. L42101 for, "Homo sapiens (subclone 10.sub.-- g10 from P1 H23) DNA sequence" May, 1995. |
GenBank.RTM. Accession No. L81793 for, "Homo sapiens (subclone 2.sub.-- d6 from P1 H28) DNA sequence, complete sequence" Apr., 1997. |
GenBank.RTM. Accession No. U51280 for, "Human chromosome 11 cosmid cSRL-183c2 containing Cys-tRNA synthetase (CARS) gene" Apr., 1996. |
GenBank.RTM. Accession No. U52111 for "Human Xq28 genomic DNA in the region of the ALD locus containing the genes for creatine transporter (SLC6A8), CDM, adrenoleukodystrophy (ALD), Na+-isocitrate dehydrogenase gamma subunit (IDH), and translocon-associated protein delta (TRAP) genes, complete cds, plexin related protein (PLEXR) and serine kinase (SK) genes, partial cds, Xq281u1 gene and cytochrome C (CCp) pseudogene" Oct., 1996. |
GenBank.RTM. Accession No. U52112 for, "Human Xq28 genomic DNA in the region of the L1CAM locus containing the genes for neural cell adhesion molecule L1 (L1CAM), arginine-vasopressin receptor (AVPR2), C1 p115 (C1), ARD1 N-acetyltransferase related protein (TE2), renin-binding protein (RbP), host cell factor 1 (HCF1), and interleukin-1 receptor-associated kinase (IRAK) genes, complete cds, and Xq281u2 gene" Oct., 1996. |
GenBank.RTM. Accession No. U72789 for, "Human cosmid U197H5, complete sequence" Oct., 1996. |
GenBank.RTM. Accession No. U80459 for, "Human Xq13 5' end of PAC 92E23 containing the X inactivation transcript (XIST) gene, complete sequence" Apr., 1997. |
GenBank.RTM. Accession No. U81831 for, "Human cosmid LL12NC01-67C6, ETV6 gene, intron 1A, partial sequence" Jan., 1997. |
GenBank.RTM. Accession No. U82213 for, "Human chromosome 10 clone LA10NC01.sub.-- 6.sub.-- E.sub.-- 6, complete sequence" Jan., 1997. |
Gen Bank.RTM. Accession No. U91323, "Human chromosome 16p13 BAC clone CIT987SK-972D3 complete sequence" Mar., 1997. |
GenBank.RTM. Accession No. U91324 for, "Human chromosome 2 BAC clone CIT987SK-100B4 complete sequence" Mar., 1997. |
GenBAnk.RTM. Accession No. U91325 for, "Human chromosome 16p13.11 BAC clone CIT987SK-731F11 complete sequence" Mar., 1997. |
GenBank.RTM. Accession No. U95739 for, "Human chromosome 16p11.2-p12 BAC clone CIT987SK-224D6 complete sequence" Apr., 1997. |
GenBank.RTM. Accession No. U95740 for, "Human chromosome 16p13.1 BAC clone CIT987SK-362G6 complete sequence" Apr., 1997. |
GenBank.RTM. Accession No. U95742 for, "Human chromosome 16p13.1 BAC clone CIT987SK-551G9 complete sequence" Apr., 1997. |
GenBank.RTM. Accession No. U96629 for, "Human chromosome 8 BAC clone CIT987SK-2A8 complete sequence" Apr., 1997. |
GenBank.RTM. Accession No. Y08683 for, "H. sapiens mRNA for carnitine palmitoyltransferase I type II" Mar., 1997. |
GenBank.RTM. Accession No. Y10196 for, "H sapiens PEX gene" Jul., 1997. |
GenBank.RTM. Accession No. Z68129 for, "H. sapiens IDH gamma gene and TRAP delta gene" Jun., 1997. |
GenBank.RTM. Accession No. Z68276 for, "Human DNA sequence from cosmid L190B4, Huntington's Disease Region, chromosome 4p16.3" Apr., 1996. |
GenBank.RTM. Accession No. Z68756 for, "Human DNA sequence from cosmid L191F1, Huntington's Disease Region, chromosome 4p16 3 contains Huntington Disease (HD) gene, CpG island ESTs and U7 small nuclear RNA" Mar., 1996. |
GenBank.RTM. Accession No. Z70280 for, "Human DNA sequence from cosmid V210E9, between markers DXS366 and DXS87 on chomosome X" Mar., 1996. |
GenBank.RTM. Accession No. Z73420 for, "Human DNA sequence from cosmid E146D10, on chromosome 22q11.2-qter, Contains rhodanese, rohu gene and ESTs" Jun., 1997. |
GenBank.RTM. Accession No. Z73496 for, "Human DNA sequence from cosmid cU120E2, on chromosome X contains Lowe oculocerebrorenal syndrome (OCRL) ESTs and STS" Nov., 1996. |
GenBank.RTM. Accession No. Z73967 for, "Human DNA sequence from cosmid 315B17, between markers DXS366 and DXS87 on chromosome X contains ESTs" Jun., 1996. |
GenBGank.RTM. Accession No. Z73988 for, "Human DNA sequence from cosmid N120B6 on chromosome 22q12-qter" Jun., 1997. |
GenBank.RTM. Accession No. Z74739 for, "Human DNA sequence from PAC 214K23, BRCA2 gene region chromosome 13q12-13 contains BRCA2 exons 1-24, Interferon Induced 56Kd pseudogene and ESTs" Apr., 1997. |
GenBank.RTM. Accession No. Z75744 for, "Human DNA sequence from cosmid N117B5 on chromosome 22q12-qter contains EST" Jul., 1996. |
GenBank.RTM. Accession No. Z79996 for, "Human DNA sequence from cosmid B33F2 on chromosome 22q11.2-qter contains ESTs" Jun., 1997. |
GenBank.RTM. Accession No. Z81315 for, "Human DNA sequence from fosmid F62D4 on chromosome 22q12-qter" Oct., 1996. |
GenBank.RTM. Accession No. Z81330 for, "Human DNA sequence from cosmid H2A1KLT on chromosome 9q34 contains ORFX gene, STS" Nov., 1996. |
GenBank.RTM. Accession No. Z82205 for, "Human DNA sequence from PAC 363L9 on chromosome X, contains STS and polymorphic CA repeat" May, 1997. |
GenBank.RTM. Accession No. Z82251 for, "Human DNA sequence from clone N87F1" Nov., 1996. |
GenBank.RTM. Accession No. Z82975 for, "Human DNA sequence from PAC 36J3, between markers DXS1192 and DXS102 on chromosome X" Nov., 1996. |
GenBank.RTM. Accession No. Z83820 for, "Human DNA sequence from PAC 215K18 on chromosome X contains ESTs and STS" Mar., 1997. |
GenBank.RTM. Accession No. Z83821 for, "Human DNA sequence from PAC 296K21 on chromosome X contains cytokeratin exon, delta-aminolevulinate synthase (erythroid), 5-aminolevulinic acid synthase. (EC 2.3.1.37), 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase (EC 2.7.1.105, EC 3.1.3.46), ESTs and STS" Mar., 1997. |
GenBank.RTM. Accession No. Z84474 for, "Human DNA sequence from PAC 111M5 on chromosome 6 Contains BBC1, RFP finger protein, EST, tRNAs, and polymorphic repeat" Mar., 1997. |
GenBank.RTM. Accession No. Z86000 for, "Human DNA sequence from PAC 151B14 on chromosome 22q12-qter contains somatostatin receptor subtype 3 (SSTR3), tRNA, ESTs, CpG island and STS" Feb., 1997. |
GenBank.RTM. Accession No. Z94057 for, "Human DNA sequence from PAC 518E13 on chromosome 1, Contains tenascin-R (restrictin) ESTs and STS" Jun., 1997. |
GenBank.RTM. Accession No. AA506343 for, "ni15a11.s1 NCI.sub.-- CGAP.sub.-- Co4 Homo sapiens cDNA clone 968060 similar to gb:D38081 Thromboxane A2 Receptor (Human); contains element PTR5 repetitive element" Jul., 1997. |
GenBank.RTM. Accession No. AC000003 for, "Genomic sequence from Human 17, complete sequence" Jun., 1997. |
GenBank.RTM. Accession No. AC000045 for, "00064,complete sequence" Oct., 1996. |
GenBank.RTM. Accession No. AC000063 for, "Human cosmid clone LUCA19 from 3p21.3, complete sequence" Nov., 1996. |
GenBank.RTM. Accession No. AC000065 for, "Human BAC clone RG085C05 from 7q21-7q22, complete sequence" Nov., 1996. |
GenBank.RTM. Accession No. AC000117 for, "Human BAD clone RG062A19 from 7q22, complete sequence" Jan., 1997. |
GenBank.RTM. Accession No. AC000118 for, "Human BAC clone RG072E11 from 7q21-7q22, complete sequence" Jan., 1997. |
GenBank.RTM. Accession No. AC000966 for, "Homo sapiens (subclone 1.sub.-- a7 from P1 H28) DNA sequence, complete sequence" Apr., 1997. |
GenBank.RTM. Accession No. AC001228 U90582 for, "244Kb Contig from Human Chromosome 11p15.5 spanning D11S1 through D11S25, complete sequence" Apr., 1997. |
GenBank.RTM. Accession No. AC002040 for, "Homo sapiens Chromosome 16 BAC clone CIT987-SK142A6 complete genomic sequence, complete sequence" Jun., 1997. |
GenBank.RTM. Accession No. AC002070 for, "Huamn BAC clone 7E17 from 12q, complete sequence" May, 1997. |
GenBank.RTM. Accession No. AC002072 for, "Human PAC clone DJ218B13 from Xq23, complete sequence" May, 1997. |
GenBank.RTM. Accession No. AC002074 for, "Human BAC clone GS056H18 from 7q31-q32, complete sequence" May, 1997. |
GenBank.RTM. Accession No. AC002076 for, "Human BAC clone GS345D13 from 7q31-q32, complete sequence" May, 1997. |
GenBank.RTM. Accession No. AC002314 for, "Human DNA from chromosome 19 cosmid R28052, genomic sequence, complete sequence" Jul., 1997. |
GenBank.RTM. Accession No. AD000092 for, "Homo sapiens DNA from Chromosome 19p13.2 cosmids R31240, R30272 and R28549 containing the EKLF, GCDH, CRTC, and RAD23A genes, genomic sequence" Apr., 1997. |
GenBank.RTM. Accession No. AD000823 for, "Homo sapiens DNA from chromosome 19-cosmid R31874, genomic sequence" Feb., 1997. |
GenBank.RTM. Accession No. AD000827 for, "Homo sapiens DNA from chromosome 19-cosmid R31158" Feb., 1997. |
GenBank.RTM. Accession No. AD000833 for "Homo sapiens DNA from chromosome 19-cosmid f19399 (.about.17 kb EcoRI restriction fragment)" Feb., 1997. |
GenBank.RTM. Accession No. AF001548 for, "Homo sapiens chromosome 16 BAC clone CIT987SK-815A9 complete sequence" May., 1997. |
GenBank.RTM. Accession No. AF001550 for, "Homo sapiens chromosome 16 BAC clone CIT987SK-334D11 complete sequence" May, 1997. |
Abdulla, S. et al., "Divergent Intron Arrangement in the MB1/LMP7 Proteasome Gene Pair," Immunogenetics, vol. 44, 254-258 (1996). |
Altschul, S.F. et al., "Basic Local Alignment Search Tool," J. Mol. Biol., vol. 215, 403-410 (1990). |
Andersson, B. et al., "Complete Sequence of a 38.4-kb Human Cosmid Insert Containing the Polymorphic Marker DXS455 from Xq28," DNA Seq., vol. 5, No. 4, 219-223 (1995). |
Andre, C. et al., "Sequence Analysis of Two Genomic Regions Containing the KIT and the FMS Receptor Tyrosine Kinase Genes," Genomics, vol. 39, 216-226 (1997). |
Beck, S. et al., "Evolutionary Dynamics of Non-Coding Sequences Within the Class II Region of the Human MHC," J. Mol. Biol., vol. 255, 1-13 (1996). |
Bouffard, G.G. et al., "A Collection of 1814 Human Chromosome 7-Specific STSs," Genome Res., vol. 7, 59-64 (1997). |
Christmanson, L. et al., "The Human Islet Amyloid Polypeptide (IAPP) Gene Organization, Chromosomal Localization and Functional Identification of a Promote Region," FEBS lett., vol. 267, No. 1, 160-166 (1990). |
Claverie, J.M. and Makalowski, W., "Alu Alert," Nature, vol. 371 p. 752 (1994). |
Francis, F. et al., "Genomic Organization of the Human PEX Gene Mutated in X-Linked Dominant Hypophosphatemic Rickets," Genome Res., vol. 7, No. 6, 5735-85 (1997). |
Gong, W. et al., "A Transcription Map of the DiGeorge and Velo-Cardio-Facial Syndrome Minimal Critical Region on 22q11," Hum. Mol. Genet., vol. 5, No. 6, 789-800 (1996). |
Gottlieb, S. et al., "The DiGeorge Syndrome Minimal Critical Region Contains a Goosecoid-like (GSCL) Homeobox Gene that is expressed Early in Human Development," Am. J. Hum. Genet., vol. 60, 1194-1201 (1997). |
Imbeaud, S. et al., "Insensitivity to Anti-Mullerian Hormone Due to a Mutation in the Human Anti-Mullerian Hormone Receptor," Nat. Genet., vol. 11, 38238-8 (1995). |
Jurka, J. and Milosavljevic, A., "Reconstruction and Analysis of Human Alu Genes," J. Mol. Evol., vol. 32, 105-121 (1991). |
Kato, N. et al., "Localization of the Rat Stimulatory G-Protein Alpha Subunit (GNPAS) Gene to Rat Chromosome 3 by Linkage Analysis," Mamm. Genome, vol. 7, No. 8, 628-629 (1996). |
Kornreich, R. et al., "Nucleotide Sequence of the Human .alpha.-Galactosidase A Gene," Nucleic Acids Res., vol. 17, no. 8, 3301-3302 (1989);. |
Kuchinke, W. et al., "Identification of mRNAs Regulted by Interferon-.gamma. in Cultured Rat Astrocytes by PCR Differential Display," Neuroimmunomodulation, vol. 2, 347-355 (1995). |
Lamerdin, J.E. et al., "Sequence Analysis of the ERCC2 Gene Regions in Human, Mouse, and Hamster Reveals Three Linked Genes," Genomics, vol. 34, 399-409 (1996). |
Lennard, A. et al., "Cloning and Chromosome Mapping of the Human Interleukin-1 Receptor Antagonist Gene," Cytokine, vol. 4, No. 2, 83-89 (1992). |
Matassi, G. et al., "Characterization of the Recombination Hot Spot Involved in the Genomic Rearrangement Leading to the Hybrid D-CE-D Gene in the D.sup.VI Phenotype," Am. J. Hum. Genet., vol. 60, 808-817 (1997). |
Oeltjen, J.C. et al., "Sixty-nine Kilobases of Contiguous Human Genomic Sequence Containing the .alpha.-Galactosidase A and Bruton's Tyrosine Kinase Loci," Mamm. Genome, vol. 6, 334-338 (1995). |
Pyerin, W., "Human Casein Kinase II: Structures, Genes, Expression and Requirement in Cell Growth Stimulation," Advan. Enzyme Regul., vol. 34, 225-246 (1994). |
Rao, E. et al., "Pseudoautosomal Deletions Encompassing a Novel Homeobox Gene Cause Growth Failure in Idiopathic Short Stature and Turner Syndrome," nature Genet., vol. 16, 54-63 (1997). |
Roark, J.H. et al., "Breakdown of B Cell Tolerance in a Mouse Model of Systemic Lupus Erythematosus," J. Exp. Med., vol. 181, 1157-1167 (1995). |
Sinnett, D. et al., "Alu RNA Transcripts in Human Embryonal Carcinoma Cells Model of Post-transcriptional Selection of Master Sequences," J. Mol. Biol., vol. 226, 689-706 (1992). |
Stenman, G. et al., "Regional Assignment of the Human 4-Hydroxyphenylpyruvate Dioxygenase Gene (HPD) to 12q24.fwdarw.qter by Fluorescence in Situ Hybridization," Cytogenet. Cell Genet., vol.71, 374-376 (1995). |
Tsukada, S. et al., "Deficient Expression of a B Cell Cytoplasmic Tyrosine Kinase in Human X-Linked Agammaglobulinemia," Cell, vol. 72, 279-290 (1993). |
van Heyningen, V. and Little, P.F.R., "Report of the Fourth International Workshop on Human Chromosome 11 Mapping 1994" Cytogenet. Cell Genet., vol. 69, 127-58 (1995). |
Vetrie, D. et al., "The Gene Involved in X-Linked Agammaglobulinaemia is a Member of the src Family of Protein-Tyrosine Kinases," Nature, vol. 361, 226-233 (1993). |
Virkkunen, P. et al., "Structural Comparison of Human and Rat Prostate-Specific Acid Phosphatase Genes and Their Promoters: Identificaton of Putative Androgen Response Elements," Biochem. and Biophys. Res. Commun., vol. 202, no. 1, 49-57 (1994). |
Vorechovsky, I. et al., "Isolation of Cosmid and cDNA Clones in the Region Surrounding the BTK Gene at Xq21.3-q22," Genomics, vol. 21, 517-524 (1994). |
Wiginton, D.A. et al., "Complete Sequence and Structure of the Gene for Human Adenosine Deaminase," Biochemistry, vol. 25, 8234-8244 (1996). |
Xiao, L. and Casero, R., "Differential Transcription of the Human Spermidine/Spermine N.sup.1 -Acetyltransferase (SSAT) Gene in Human Lung Carcinoma Cells," Biochem. J., vol. 313, 691-696 (1996). |
Copy of GenBank.RTM. search using nucleotide sequence mouse siva gene. |
Fitzgerald, L. A. et al., "Protein Sequence of Endothelial Glycoprotein IIIa Derived from a cDNA Clone," J. Biol. Chem, vol. 262, no. 9, 3936-3939 (1987). |
Frachet, P. et al., "GPIIb and GPIIa Amino Acid Sequences Deduced from Human Megakaryocyte cDNAs," Mol. Biol. Rep., vol. 14, 27-33 (1990). |
Lanza, F. et al., "Characterization of the Human Platelet Glycoprotein IIIa Gene," J. Biol. chem., vol. 265, no. 30, 18098-18103 (1990). |
Prasad, K.V.S. et al., "CD27, a Member of the Tumor Necrosis Factor Receptor Family, Induces Apoptosis and Binds to Siva, a Proapoptotic Protein," PNAS USA, vol. 94, 6346-6351 (1997). |
Zimrin, A.B. et al., "Structure of Platelet Glycoprotein IIIa A Common Subunit for Two Different Membrane Receptors," J. Clin. Invest., vol. 81, 1470-1475 (1988). |
Zimrin, A.B. et al., "The Genomic Organization of Platelet Glycoprotein IIIa," J. Biol. Chem., vol. 265, No. 15, 8590-8595 (1990). |