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Mammalian Genome 8, $27-$49 (1998).
Mammal ian Genome ........
�9 Springer-Verlag New York Inc. 1998
Mouse Chromosome 2
Josephine Peters, 1'* Linda D. Siracusa, 2'** Daniel P o m p , 3 A a m i r R. Zuberi , 4 Deanna Church, 5 Revati Koratkar , 2 Catherine M. Abbot t 6
1Mammalian Genetics Unit, Medical Research Council, Didcot, Oxon OX11 0RD, UK ajefferson Cancer Center, Jefferson Medical College, Department of Microbiology and Immunology, 233 South 10th Street, Philadelphia, Pennsylvania 19107-5541, USA 3Department of Animal Science, University of Nebraska-Lincoln, Lincoln, Nebraska 68583-0908, USA 4The Jackson Laboratory, 600 Main Street, Bar Harbor, Maine 04609, USA SSamuel Lunenfeld Research Institute, Mt. Sinai Hospital, Rm 884, 600 University Avenue, Toronto, Ontario MG5 1X5, Canada 6Human Genetics Unit, Molecular Medicine Centre, The University of Edinburgh, Western General Hospital, Crewe Road, Edinburgh EH4 2XU, UK
Received: 1 December 1997
Introduction
This report collates information about the genetic organization of mouse Chromosome 2 (Chr 2). A consensus linkage map of Chr 2 was generated based on a foundation of genetic crosses in which multiple loci were mapped, providing the relative order of loci along the length of the chromosome. The remaining loci were subsequently added to produce a map that serves as a guide for genetic, molecular, and physical analyses. The consensus map is not absolute; locus positions are reassessed each year and may change, since new information is continually integrated into the map.
determined and that the estimated location of each locus is inher- ently subject to significant error. Furthermore, evidence suggesting the presence of a QTL may also be indicative of two or more tightly linked loci that cannot be separated statistically. All QTL listed have been detected with forms of interval analysis with significant levels of LOD (3.0 or P < 0.001), or have been con- firmed in multiple crosses or in congenic lines. The electronic version of this report shows a range of position for each QTL listed in Table 1.
Identification of YACs that carry Chr 2 markers
Locus list
Table 1 now lists more than 1100 loci on mouse Chr 2. The asterisk (*) in the first column indicates the new loci assigned to mouse Chr 2 since the last report. Fifty-seven new genes including two new mutations, sooty foot (soo) and ebouriffe (ebo), 91 new DNA markers, and 6 new quantitative trait loci (QTL) have been added. It has been established that pa is not Epb4.2 (38773). The gene for lethal milk was reported to be a zinc transporter (Znt4) at the 1 lth IMGS by Huang and Gitschier. The microsatellite loci, D2Mit301-D2Mit530, have been added; up-to-date listings can be obtained by contacting the Whitehead Institute/MIT Center for Genome Research at http:/www-genome.wi.mit.edu. The D2Cph loci (10555) and D2Ncvs loci (21638) have not yet been included.
The consensus map was constructed by first creating a skeleton map based predominantly on multilocus backcross analysis. Data from three and four-point crosses were next incorporated, and loci mapped only in two-point crosses were added last. Placement of loci mapped only in RI strains was estimated by averaging interval distances between flanking markers. Some histocompatibility loci were positioned by analysis of congenic strains.
The consensus map should be used as a guide for gene local- ization. Gene order is established unambiguously only for those loci mapped in the same cross. Order for closely linked genes that have not yet been mapped with respect to each other was inferred on the basis of recombination distances.
Quantitative trait loci (QTL)
Twenty QTL have now been assigned to mouse Chr 2. It is im- portant to note that the true identity of each QTL has not yet been
* Chair ** Co-Chair Correspondence to: J. Peters
Chr 2 containing YACs are listed in the electronic version of this report. The libraries screened include the Princeton and the origi- nal Whitehead/MIT C57BL/6 YAC libraries, and the combined St. Mary's and ICRF C57BL/10 and C3H libraries (available through the Baylor College of Medicine). Information concerning Chr 2 YACs der ived from the more recent Whi tehead/MIT-820 C57BL/6 library can be accessed at http://www.informatics.jax. org/mitmaps.html.
Comparative maps
Mouse Chr 2 shows regions of conserved homology with human Chrs 2, 7, 9, 10, 11, 15, and 20. Table 1 lists the 179 loci mapping to mouse Chr 2 that have also been localized in the human genome, along with their corresponding human gene symbol and human chromosomal location. The Online Mendelian Inheritance in Man database and the Genome DataBase provide references for the mapping of human homologs.
Legend for Chromosome Committee Map
The information about each locus for a chromosome appears on one line of the map. At the left is a small figure of the whole chromosome. A box on the chromosome figure indicates which portion of the chromosome is expanded for view on that page. To the right of the small figure is the corresponding expanded cen- timorgan scale. For each locus on the chromosome a line extends from the scale to the marker or group of markers at that position. From left-to-right, the columns are:
Symbol New
an asterisk * appears in the column if this is a newly discovered locus since the last published committee report
$28 J. Peters et al.: Mouse Chromosome 2
Confidence of placement on the map filled circles = high confidence, mapping to high resolution in at least one cross with multiple other loci; half-filled circles = intermediate confidence, mapping in one or few crosses relative to one or a few markers; or open circles = low confidence, e.g., mapping by in-situ hybridization only or in a QTL-analysis
Name of locus an asterisk incidates name is truncated at 50 characters
Method of localization L = linkage crosses; I = in-situ hybridization; S = somatic cell hybridization studies; H = radiation cell hybrids; R = RI strain analysis; C = cytogenetic assignment; D = deletion analysis; P = physical mapping; T = partial t-haplotype analy- sis; 0 = other
Trait a 'T ' in the column indicates that the locus has known associ- ated phenotypic traits
Cytogenetic Band Human Homolog
symbol of the human gene if a human homolog is known Human Location
human cytogenetic localization for the homolog up to four Reference Numbers;
in the Mouse Genome Database, reference numbers are of the form J : # ~ ; these numbers represent the ~ # portion of this identifier. Additional references may be available through the Web.
Acknowledgments. Comments on the map are welcomed. We apologize for omissions and respectfully request investigators to send the missing pieces. We thank investigators who generously shared their unpublished results. We thank the staff of the Mouse Genome Database for their help. We are grateful to Rachael Selley for excellent assistance.
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MIT
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MIT
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MIT
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MIT
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3
Ref
eren
ces
2013
3 10
66,2
3388
10
66,2
3388
22
461
2246
1 22
461
3413
6 34
136
3413
6 34
136
2073
8 34
136
3413
6 20
133,
2004
1 28
411
2246
1 62
10
2151
0 20
410
2912
6,34
960
2246
1 81
18
3413
6 17
235
2013
3,22
207,
2244
6 88
88,9
413
2338
8 22
461
2246
1 34
136
3413
6 34
136
3413
6 20
038,
2279
8,24
190,
3879
39
021
2624
0,31
804
1483
0 37
096
1043
9 23
388
3413
6 34
136
1048
9 29
126
2912
6 17
235,
2311
4
3413
6 29
126
2419
3 17
330,
1897
3,22
019
3379
9 13
63
1723
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114
2419
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@
r o
Sym
bol
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pl
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in in
lens
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Chr
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seg
men
t, C
hr 2
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Naz
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le T
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Chr
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seg
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hr 2
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umod
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seg
men
t, C
hr 2
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NA
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hr 2
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don
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14
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Chr
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seg
men
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hr 2
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don
16
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Chr
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D
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seg
men
t, C
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D
NA
seg
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D
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seg
men
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seg
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ta F
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dele
tion,
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5 de
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n, C
hr 2
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wel
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dupl
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2, H
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doge
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L 29
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Sym
bol
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k In
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OR
k In
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New
C
on f,
N
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n, C
hr 2
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in
vers
ion,
Chr
2, R
oder
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4O
inve
rsio
n, C
hr 2
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45
inve
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n, C
hr 2
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58
inse
rtion
, Chr
17
piec
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to in
verte
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hr 2
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t of
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mat
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na
tura
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d an
tigen
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Dro
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trans
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fact
or r
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ed, I
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poly
tropi
c m
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63
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tor,
endo
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pho
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tase
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r typ
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tran
sloc
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n, C
hr 2
and
4, D
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proc
al tr
ansl
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Chr
2 a
nd 6
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isso
n-97
re
cipr
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tran
sloc
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n, C
hr 2
and
8, A
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reci
proc
al tr
ansl
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lon,
Chr
2 a
nd 1
1 D
avis
son-
4 re
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tran
sloc
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n, C
hr 2
and
12
Dav
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proc
al tm
nslo
catio
n, C
hr 2
and
14
Gan
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proc
al tr
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Chr
2 a
nd 1
5, A
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reci
proc
al tr
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Chr
2 a
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9, H
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thal
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body
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duce
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late
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rel
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mal
spe
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D
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seg
men
t, C
hr 2
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enm
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25
DN
A s
egm
ent,
Chr
2, B
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mei
er 2
7, e
xpre
ssed
D
NA
seg
men
t, C
hr 2
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mei
er 2
8, e
xpre
ssed
D
NA
seg
men
t, C
hr 2
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m &
Wom
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Gen
etic
s 01
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NA
seg
men
t, C
hr 2
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Chr
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~ D
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seg
men
t, C
hr 2
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Chr
2, B
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NA
seg
men
t, C
hr 2
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Chr
2,
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A s
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13"
ham
& W
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13"
DN
A s
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ent,
Chr
2, B
ri ha
m &
Wom
en's
Gen
etic
s 14
" D
NA
seg
men
t, C
hr 2
, Den
y C
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peni
an 1
D
NA
seg
men
t, C
hr 2
, G. C
onsa
lez
1, e
xpre
ssed
D
NA
seg
men
t, C
hr 2
, G. C
onsa
lez
2, e
xpre
ssed
D
NA
seg
men
t, C
hr 2
, G. C
onsa
lez
3, e
xpre
ssed
D
NA
seg
men
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Ref
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4 24
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4 37
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3722
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3722
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126
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2 17
854
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4,34
884
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