Symbol Name ID Chromosome |
Ess2
ess-2 splicing factor MGI:107854 16 |
Experiment Type | Details | Chromosome | Reference |
---|---|---|---|
FISH |
Band: B1-B3 |
16 | J:44451 Botta A, et al., Comparative mapping of the DiGeorge syndrome region in mouse shows inconsistent gene order and differential degree of gene conservation. Mamm Genome. 1997 Dec;8(12):890-5 |
FISH |
Band: B1-B3 |
16 | J:35457 Rizzu P, et al., Cloning and comparative mapping of a gene from the commonly deleted region of DiGeorge and Velocardiofacial syndromes conserved in C. elegans. Mamm Genome. 1996 Sep;7(9):639-43 |
TEXT | 16 | J:38617 Gong W, et al., Structural and mutational analysis of a conserved gene (DGSI) from the minimal DiGeorge syndrome critical region. Hum Mol Genet. 1997 Feb;6(2):267-76 | |
TEXT | 16 | J:110101 Paylor R, et al., Tbx1 haploinsufficiency is linked to behavioral disorders in mice and humans: implications for 22q11 deletion syndrome. Proc Natl Acad Sci U S A. 2006 May 16;103(20):7729-34 | |
TEXT-Physical Mapping | 16 | J:44451 Botta A, et al., Comparative mapping of the DiGeorge syndrome region in mouse shows inconsistent gene order and differential degree of gene conservation. Mamm Genome. 1997 Dec;8(12):890-5 | |
TEXT-Physical Mapping | 16 | J:58432 Kimber WL, et al., Deletion of 150 kb in the minimal DiGeorge/velocardiofacial syndrome critical region in mouse. Hum Mol Genet. 1999 Nov;8(12):2229-37 | |
TEXT-Physical Mapping | 16 | J:60871 Lund J, et al., Comparative sequence analysis of 634 kb of the mouse chromosome 16 region of conserved synteny with the human velocardiofacial syndrome region on chromosome 22q11.2. Genomics. 2000 Feb 1;63(3):374-83 | |
TEXT-Physical Mapping | 16 | J:54501 Lund J, et al., Sequence-ready physical map of the mouse chromosome 16 region with conserved synteny to the human velocardiofacial syndrome region on 22q11.2. Mamm Genome. 1999 May;10(5):438-43 | |
TEXT-Physical Mapping | 16 | J:45079 Puech A, et al., Comparative mapping of the human 22q11 chromosomal region and the orthologous region in mice reveals complex changes in gene organization. Proc Natl Acad Sci U S A. 1997 Dec 23;94(26):14608-13 | |
TEXT-Physical Mapping | 16 | J:64380 Puech A, et al., Normal cardiovascular development in mice deficient for 16 genes in 550 kb of the velocardiofacial/DiGeorge syndrome region. Proc Natl Acad Sci U S A. 2000 Aug 29;97(18):10090-5 | |
TEXT-Physical Mapping | 16 | J:83362 Shiohama A, et al., Molecular cloning and expression analysis of a novel gene DGCR8 located in the DiGeorge syndrome chromosomal region. Biochem Biophys Res Commun. 2003 Apr 25;304(1):184-90 | |
TEXT-Physical Mapping | 16 | J:49844 Sutherland HF, et al., Cloning and comparative mapping of the DiGeorge syndrome critical region in the mouse. Genomics. 1998 Aug 15;52(1):37-43 | |
TEXT-Physical Mapping | 16 | J:80000 The FANTOM Consortium and The RIKEN Genome Exploration Research Group Phase I & II Team, Analysis of the mouse transcriptome based on functional annotation of 60,770 full-length cDNAs. Nature. 2002;420:563-573 | |
TEXT-QTL | 16 | J:38193 Galili N, et al., A region of mouse chromosome 16 is syntenic to the DiGeorge, velocardiofacial syndrome minimal critical region. (Correction: vol. 7(4):399). Genome Res. 1997 Jan;7(1):17-26 | |
TEXT-Radiation Hybrid | 16 | J:68900 The Jackson Laboratory Mouse Radiation Hybrid Database, Mouse T31 Radiation Hybrid Data Load. Database Release. 2004; |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
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last database update 12/10/2024 MGI 6.24 |
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