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Dp(16Cbr1-Fam3b)1Rhr
Cytogenetic Marker Detail
Symbol

Name
ID
Dp(16Cbr1-Fam3b)1Rhr
duplication, Chr 16, H R Reeves 1
MGI:3487250
Synonyms
Dp(16Cbr1-ORF9)1Rhr, Is(16Cbr1-ORF9)1Rhr, Is(16Mx2-Cbr1)1Rhr, Is(16Mx2-Cbrl)1Rhr, Ts(1616)1Rhr
Feature Type
chromosomal duplication
Genetic Map
Chromosome 16
Syntenic

Mapping data(1)
Sequence Map
Chr16:93607837-97504936 bp
From MGI annotation of GRCm38

  3897100 bp   ±  kb flank

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Mouse Genome Browser
Mutations,
alleles, and
phenotypes
All mutations/alleles(1) : Targeted(1)
Human Diseases Modeled in Mice Using Dp(16Cbr1-Fam3b)1Rhr (1)    Mutations Annotated to Human Diseases (1)   
Polymorphisms
SNPs within 2kb(19481 from dbSNP Build 137)    SNPs within 2kb including multiple locations(19565)
References
(Earliest) J:93223 Olson LE, et al., A chromosome 21 critical region does not cause specific down syndrome phenotypes. Science. 2004 Oct 22;306(5696):687-90
(Latest) J:212324 Lane AA, et al., Triplication of a 21q22 region contributes to B cell transformation through HMGN1 overexpression and loss of histone H3 Lys27 trimethylation. Nat Genet. 2014 Jun;46(6):618-23
All references(15)
Disease annotation references (3)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
07/21/2015
MGI 5.22
The Jackson Laboratory