Mapping Data Summary

• Symbol: Limk1
• Name: LIM domain kinase 1
• ID: MGI:104572
• Chromosome: 5

19 mapping experiments

Experiment Type	Details	Chromosome	Reference
CROSS	Cross Type: Backcross Mapping Panel: JAX (BSS)	5	J:68983 Durkin ME, et al., Integration of a c-myc Transgene Results in Disruption of the Mouse Gtf2ird1 Gene, the Homologue of the Human GTF2IRD1 Gene Hemizygously Deleted in Williams-Beuren Syndrome. Genomics. 2001 Apr 1;73(1):20-7
CROSS	Cross Type: Backcross Mapping Panel: JAX (BSS)	5	J:39491 Gao Z, et al., Chromosome localization of the mouse zonadhesin gene and the human zonadhesin gene (ZAN). Genomics. 1997 Apr 1;41(1):119-22
CROSS	Cross Type: Backcross Mapping Panel: JAX (BSS)	5	J:43669 Himmelbauer H, et al., IRS-PCR-based mapping of the Huntingtin interacting protein (HIP1) on mouse Chromosome 5. Mamm Genome. 1998 Jan;9(1):26-31
CROSS	Cross Type: Backcross Mapping Panel: JAX (BSS)	5	J:43669 Himmelbauer H, et al., IRS-PCR-based mapping of the Huntingtin interacting protein (HIP1) on mouse Chromosome 5. Mamm Genome. 1998 Jan;9(1):26-31
CROSS	Cross Type: Backcross Mapping Panel: JAX (BSS)	5	J:58545 Perez Jurado LA, et al., TBL2, a novel transducin family member in the WBS deletion: characterization of the complete sequence, genomic structure, transcriptional variants and the mouse ortholog. Cytogenet Cell Genet. 1999;86(3-4):277-84
CROSS	Cross Type: Backcross Mapping Panel: JAX (BSS)	5	J:29439 Proschel C, et al., Limk1 is predominantly expressed in neural tissues and phosphorylates serine, threonine and tyrosine residues in vitro. Oncogene. 1995 Oct 5;11(7):1271-81
CROSS	Cross Type: Backcross Mapping Panel: JAX (BSS)	5	J:40407 Sutton VR, et al., Regional localization of the mouse argininosuccinate lyase gene to chromosome 5. Mamm Genome. 1997;8(11):871
CROSS	Cross Type: Backcross Mapping Panel: JAX (BSS)	5	J:65086 Valero MC, et al., Fine-scale comparative mapping of the human 7q11.23 region and the orthologous region on mouse chromosome 5G: the low-copy repeats that flank the williams-beuren syndrome deletion arose at breakpoint sites of an evolutionary inversion(s) [In Process Citation]. Genomics. 2000 Oct 1;69(1):1-13
CROSS	Cross Type: Backcross Mapping Panel: JAX (BSS)	5	J:43550 Wang YK, et al., A mouse single-copy gene, Gtf2i, the homolog of human GTF2I, that is duplicated in the Williams-Beuren syndrome deletion region. Genomics. 1998 Mar 1;48(2):163-70
FISH	Band: G1	5	J:36719 Mao X, et al., Assignment of the human and mouse LIM-kinase genes (LIMK1; Limk1) to chromosome bands 7q11.23 and 5G1, respectively, by in situ hybridization. Cytogenet Cell Genet. 1996;74(3):190-1
IN SITU	Band: G2	5	J:34622 Bernard O, et al., Structure and chromosomal localization of the genomic locus encoding the Kiz1 LIM-kinase gene. Genomics. 1996 Aug 1;35(3):593-6
IN SITU	Band: G2	5	J:34622 Bernard O, et al., Structure and chromosomal localization of the genomic locus encoding the Kiz1 LIM-kinase gene. Genomics. 1996 Aug 1;35(3):593-6
TEXT-Genetic Cross		5	J:28711 Cheng AK, et al., The murine LIM-kinase gene (limk) encodes a novel serine threonine kinase expressed predominantly in trophoblast giant cells and the developing nervous system. Mech Dev. 1995 Aug;52(2-3):187-97
TEXT-Physical Mapping		5	J:73830 DeSilva U, et al., Generation and comparative analysis of approximately 3.3 Mb of mouse genomic sequence orthologous to the region of human chromosome 7q11.23 implicated in Williams syndrome. Genome Res. 2002 Jan;12(1):3-15
TEXT-Physical Mapping		5	J:55324 DeSilva U, et al., Comparative mapping of the region of human chromosome 7 deleted in williams syndrome. Genome Res. 1999 May;9(5):428-36
TEXT-Physical Mapping		5	J:55324 DeSilva U, et al., Comparative mapping of the region of human chromosome 7 deleted in williams syndrome. Genome Res. 1999 May;9(5):428-36
TEXT-Physical Mapping		5	J:64707 Martindale DW, et al., Comparative genomic sequence analysis of the williams syndrome region (LIMK1-RFC2) of human chromosome 7q11.23. Mamm Genome. 2000 Oct;11(10):890-8
TEXT-Physical Mapping		5	J:65086 Valero MC, et al., Fine-scale comparative mapping of the human 7q11.23 region and the orthologous region on mouse chromosome 5G: the low-copy repeats that flank the williams-beuren syndrome deletion arose at breakpoint sites of an evolutionary inversion(s) [In Process Citation]. Genomics. 2000 Oct 1;69(1):1-13
TEXT-Radiation Hybrid		5	J:68900 The Jackson Laboratory Mouse Radiation Hybrid Database, Mouse T31 Radiation Hybrid Data Load. Database Release. 2004;