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Symbol
Name
ID
Chromosome
Ednrb
endothelin receptor type B
MGI:102720
14
30 mapping experiments
Experiment Type Details Chromosome Reference
CROSS Cross Type: Backcross
14 J:14299 Beechey CV, Linkage studies with T(2;14)48H. Mouse Genome. 1991;89:257
CROSS Cross Type: Backcross
14 J:28912 Cattanach BM, Research News. Mouse Genome. 1995;93(3):853-61
CROSS Cross Type: Backcross
14 J:28912 Cattanach BM, Research News. Mouse Genome. 1995;93(3):853-61
CROSS Cross Type: Backcross
14 J:5291 Eicher EM, et al., The T6 translocation in the mouse: its use in trisomy mapping, centromere localization, and cytological identification of linkage group 3. Genetics. 1972 Aug;71(4):621-32
CROSS Cross Type: Backcross
14 J:102 Kidwell JF, et al., Pugnose-a recessive mutation in linkage group 3 of mice. J Hered. 1961;52:145-148
CROSS Cross Type: Backcross
14 J:102 Kidwell JF, et al., Pugnose-a recessive mutation in linkage group 3 of mice. J Hered. 1961;52:145-148
CROSS Cross Type: Intercross
14 J:102 Kidwell JF, et al., Pugnose-a recessive mutation in linkage group 3 of mice. J Hered. 1961;52:145-148
CROSS Cross Type: Backcross
14 J:5030 Kidwell JF, et al., Pugnose linkage in the mouse. J Hered. 1966 Nov-Dec;57(6):229-30
CROSS Cross Type: Backcross
14 J:5030 Kidwell JF, et al., Pugnose linkage in the mouse. J Hered. 1966 Nov-Dec;57(6):229-30
CROSS Cross Type: Backcross
14 J:5030 Kidwell JF, et al., Pugnose linkage in the mouse. J Hered. 1966 Nov-Dec;57(6):229-30
CROSS Cross Type: Backcross
14 J:42684 Koide T, et al., A new inbred strain JF1 established from Japanese fancy mouse carrying the classic piebald allele [published erratum appears in Mamm Genome 1998 Apr;9(4):344]. Mamm Genome. 1998 Jan;9(1):15-9
CROSS Cross Type: Backcross
14 J:16291 Metallinos DL, et al., Fine structure mapping and deletion analysis of the murine piebald locus. Genetics. 1994 Jan;136(1):217-23
CROSS Cross Type: Backcross
14 J:16291 Metallinos DL, et al., Fine structure mapping and deletion analysis of the murine piebald locus. Genetics. 1994 Jan;136(1):217-23
CROSS Cross Type: Backcross
14 J:62508 Okamura T, et al., Molecular cloning and characterization of mouse testis poly(A) binding protein II encoded by the Pabp3 gene, which transcomplements meiotic mutant sme2 of S. pombe. Biochem Genet. 2000 Feb;38(1-2):1-11
CROSS Cross Type: Backcross
14 J:14290 Rasberry C, et al., Location of talipes (Tal). Mouse Genome. 1990;87:89
CROSS Cross Type: Backcross
14 J:299 Snell GD, Inheritance in the House Mouse, the Linkage Relations of Short-Ear, Hairless, and Naked. Genetics. 1931 Jan;16(1):42-74
CROSS Cross Type: Single backcross
14 J:299 Snell GD, Inheritance in the House Mouse, the Linkage Relations of Short-Ear, Hairless, and Naked. Genetics. 1931 Jan;16(1):42-74
CROSS Cross Type: Backcross
14 J:299 Snell GD, Inheritance in the House Mouse, the Linkage Relations of Short-Ear, Hairless, and Naked. Genetics. 1931 Jan;16(1):42-74
CROSS Cross Type: Backcross
14 J:299 Snell GD, Inheritance in the House Mouse, the Linkage Relations of Short-Ear, Hairless, and Naked. Genetics. 1931 Jan;16(1):42-74
CROSS Cross Type: Backcross
14 J:5825 Womack JE, et al., Mapping of nucleoside phosphorylase (Np-1) and esterase 10 (Es-10) on mouse chromosome 14. Biochem Genet. 1977 Apr;15(3-4):347-55
TEXT 14 J:16291 Metallinos DL, et al., Fine structure mapping and deletion analysis of the murine piebald locus. Genetics. 1994 Jan;136(1):217-23
TEXT 14 J:33677 O'Brien TP, et al., Complementation mapping of skeletal and central nervous system abnormalities in mice of the piebald deletion complex. Genetics. 1996 May;143(1):447-61
TEXT-Genetic Cross 14 J:33677 O'Brien TP, et al., Complementation mapping of skeletal and central nervous system abnormalities in mice of the piebald deletion complex. Genetics. 1996 May;143(1):447-61
TEXT-Physical Mapping 14 J:74603 Kurihara LJ, et al., Candidate genes required for embryonic development: a comparative analysis of distal mouse chromosome 14 and human chromosome 13q22. Genomics. 2002 Feb;79(2):154-61
TEXT-Physical Mapping 14 J:78120 Peterson KA, et al., Functional and comparative genomic analysis of the piebald deletion region of mouse chromosome 14. Genomics. 2002 Aug;80(2):172-84
TEXT-Physical Mapping 14 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 14 J:118320 Owens SE, et al., Genome-wide linkage identifies novel modifier loci of aganglionosis in the Sox10Dom model of Hirschsprung disease. Hum Mol Genet. 2005 Jun 1;14(11):1549-58
TEXT-QTL 14 J:58047 Rasmussen E, et al., Identification of quantitative trait loci for haloperidol-induced catalepsy on mouse chromosome 14. J Pharmacol Exp Ther. 1999 Sep;290(3):1337-46
TEXT-QTL 14 J:89229 Ulbrich M, et al., Genetic modifiers that aggravate the neurological phenotype of the wobbler mouse. Neuroreport. 2002 Mar 25;13(4):535-9
TEXT-Radiation Hybrid 14 J:68900 The Jackson Laboratory Mouse Radiation Hybrid Database, Mouse T31 Radiation Hybrid Data Load. Database Release. 2004;

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last database update
11/07/2017
MGI 6.11
The Jackson Laboratory