Other mutations in this stock |
Total: 62 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4933434E20Rik |
T |
C |
3: 89,969,021 (GRCm39) |
S215P |
probably benign |
Het |
Ano2 |
C |
T |
6: 126,016,460 (GRCm39) |
Q998* |
probably null |
Het |
Atg9a |
A |
T |
1: 75,164,736 (GRCm39) |
V76E |
probably damaging |
Het |
Cacna1c |
T |
C |
6: 119,034,172 (GRCm39) |
I118M |
|
Het |
Cacna1g |
T |
A |
11: 94,323,383 (GRCm39) |
I1274F |
probably damaging |
Het |
Cd300lg |
C |
T |
11: 101,937,767 (GRCm39) |
A199V |
probably benign |
Het |
Cfap61 |
C |
T |
2: 145,887,390 (GRCm39) |
R612* |
probably null |
Het |
Cpeb4 |
A |
T |
11: 31,881,417 (GRCm39) |
Y692F |
probably damaging |
Het |
Dcun1d1 |
A |
G |
3: 35,951,940 (GRCm39) |
|
probably null |
Het |
Dennd2d |
T |
A |
3: 106,398,579 (GRCm39) |
M188K |
probably benign |
Het |
Dmgdh |
A |
G |
13: 93,845,354 (GRCm39) |
|
probably null |
Het |
Efl1 |
T |
A |
7: 82,330,652 (GRCm39) |
M275K |
probably benign |
Het |
Erp29 |
G |
T |
5: 121,583,392 (GRCm39) |
A178D |
probably benign |
Het |
Fbn1 |
T |
C |
2: 125,308,594 (GRCm39) |
N156S |
possibly damaging |
Het |
Frrs1 |
C |
T |
3: 116,675,426 (GRCm39) |
T118I |
probably damaging |
Het |
Frrs1l |
A |
G |
4: 56,968,230 (GRCm39) |
W181R |
probably benign |
Het |
Gprc5b |
C |
A |
7: 118,583,482 (GRCm39) |
W129L |
probably damaging |
Het |
Hoxc9 |
A |
G |
15: 102,890,593 (GRCm39) |
H170R |
probably benign |
Het |
Il12rb2 |
C |
T |
6: 67,333,617 (GRCm39) |
D221N |
probably benign |
Het |
Lmo1 |
T |
C |
7: 108,742,819 (GRCm39) |
N28S |
probably benign |
Het |
Lrrfip2 |
T |
A |
9: 111,006,525 (GRCm39) |
|
probably null |
Het |
Macf1 |
A |
T |
4: 123,400,130 (GRCm39) |
F722I |
probably damaging |
Het |
Mical1 |
T |
C |
10: 41,355,772 (GRCm39) |
|
probably null |
Het |
Mtcl3 |
A |
G |
10: 29,073,240 (GRCm39) |
Y844C |
probably damaging |
Het |
Mtmr11 |
C |
T |
3: 96,071,855 (GRCm39) |
T223M |
possibly damaging |
Het |
Mup21 |
A |
G |
4: 62,068,468 (GRCm39) |
V66A |
probably benign |
Het |
Nav2 |
C |
A |
7: 49,111,672 (GRCm39) |
A726D |
possibly damaging |
Het |
Nbeal1 |
G |
C |
1: 60,276,310 (GRCm39) |
V684L |
probably benign |
Het |
Nudt21 |
A |
T |
8: 94,746,227 (GRCm39) |
V157D |
probably benign |
Het |
Numa1 |
T |
C |
7: 101,639,806 (GRCm39) |
I52T |
possibly damaging |
Het |
Obscn |
T |
C |
11: 58,946,442 (GRCm39) |
D4421G |
probably benign |
Het |
Oog3 |
T |
C |
4: 143,886,801 (GRCm39) |
I106M |
probably benign |
Het |
Or10g9 |
A |
T |
9: 39,912,106 (GRCm39) |
V139E |
probably benign |
Het |
Or2g25 |
T |
C |
17: 37,970,403 (GRCm39) |
T274A |
possibly damaging |
Het |
Or2z9 |
T |
C |
8: 72,853,793 (GRCm39) |
L63P |
probably damaging |
Het |
Or51f1 |
T |
A |
7: 102,505,706 (GRCm39) |
Y261F |
probably damaging |
Het |
Or5w20 |
T |
G |
2: 87,726,755 (GRCm39) |
C71G |
possibly damaging |
Het |
Orai2 |
T |
A |
5: 136,179,437 (GRCm39) |
I199F |
probably damaging |
Het |
P2rx5 |
C |
A |
11: 73,055,692 (GRCm39) |
L50M |
probably damaging |
Het |
Pdia2 |
T |
C |
17: 26,416,634 (GRCm39) |
E215G |
possibly damaging |
Het |
Pds5a |
A |
T |
5: 65,823,570 (GRCm39) |
S74T |
possibly damaging |
Het |
Phlpp2 |
A |
G |
8: 110,666,785 (GRCm39) |
S1105G |
probably damaging |
Het |
Pi4kb |
T |
A |
3: 94,891,888 (GRCm39) |
D189E |
probably benign |
Het |
Pigw |
G |
A |
11: 84,768,585 (GRCm39) |
T248M |
probably damaging |
Het |
Pnlip |
T |
A |
19: 58,670,134 (GRCm39) |
V458D |
probably damaging |
Het |
Ppm1l |
G |
A |
3: 69,225,044 (GRCm39) |
V49I |
probably benign |
Het |
Prl3b1 |
T |
A |
13: 27,426,473 (GRCm39) |
M1K |
probably null |
Het |
Rad1 |
T |
A |
15: 10,493,367 (GRCm39) |
C265S |
probably benign |
Het |
Rnaset2b |
C |
T |
17: 7,265,427 (GRCm39) |
S237F |
probably benign |
Het |
S1pr2 |
T |
C |
9: 20,879,238 (GRCm39) |
I197V |
probably benign |
Het |
Smyd4 |
A |
G |
11: 75,281,082 (GRCm39) |
Q185R |
probably benign |
Het |
Sox5 |
T |
A |
6: 144,100,759 (GRCm39) |
T77S |
probably benign |
Het |
Sox7 |
A |
G |
14: 64,185,291 (GRCm39) |
Y109C |
probably damaging |
Het |
Styxl2 |
C |
T |
1: 165,954,676 (GRCm39) |
V25I |
probably damaging |
Het |
Tln1 |
G |
A |
4: 43,545,922 (GRCm39) |
R898C |
probably damaging |
Het |
Tmprss11b |
T |
A |
5: 86,812,173 (GRCm39) |
E158V |
probably damaging |
Het |
Tnpo3 |
C |
A |
6: 29,562,875 (GRCm39) |
R614L |
possibly damaging |
Het |
Vmn2r100 |
T |
A |
17: 19,742,296 (GRCm39) |
D223E |
probably benign |
Het |
Zc3h12d |
A |
T |
10: 7,743,345 (GRCm39) |
M372L |
probably benign |
Het |
Zfp28 |
G |
T |
7: 6,386,593 (GRCm39) |
|
probably benign |
Het |
Zfp963 |
A |
T |
8: 70,195,759 (GRCm39) |
H231Q |
probably damaging |
Het |
Zscan4b |
A |
G |
7: 10,634,867 (GRCm39) |
S459P |
probably benign |
Het |
|
Other mutations in Rtl1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00672:Rtl1
|
APN |
12 |
109,559,434 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01981:Rtl1
|
APN |
12 |
109,558,369 (GRCm39) |
missense |
possibly damaging |
0.72 |
IGL02418:Rtl1
|
APN |
12 |
109,556,883 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03164:Rtl1
|
APN |
12 |
109,559,367 (GRCm39) |
missense |
probably damaging |
1.00 |
FR4304:Rtl1
|
UTSW |
12 |
109,557,632 (GRCm39) |
small deletion |
probably benign |
|
R0109:Rtl1
|
UTSW |
12 |
109,561,841 (GRCm39) |
start gained |
probably benign |
|
R0141:Rtl1
|
UTSW |
12 |
109,559,382 (GRCm39) |
missense |
probably damaging |
1.00 |
R0312:Rtl1
|
UTSW |
12 |
109,556,661 (GRCm39) |
missense |
probably damaging |
0.99 |
R0389:Rtl1
|
UTSW |
12 |
109,556,797 (GRCm39) |
missense |
possibly damaging |
0.77 |
R0390:Rtl1
|
UTSW |
12 |
109,557,820 (GRCm39) |
missense |
unknown |
|
R0548:Rtl1
|
UTSW |
12 |
109,558,089 (GRCm39) |
missense |
probably damaging |
0.98 |
R0561:Rtl1
|
UTSW |
12 |
109,560,363 (GRCm39) |
missense |
probably damaging |
0.99 |
R0624:Rtl1
|
UTSW |
12 |
109,559,153 (GRCm39) |
missense |
probably damaging |
0.97 |
R0746:Rtl1
|
UTSW |
12 |
109,559,394 (GRCm39) |
missense |
probably damaging |
1.00 |
R1353:Rtl1
|
UTSW |
12 |
109,558,633 (GRCm39) |
missense |
probably benign |
0.00 |
R1868:Rtl1
|
UTSW |
12 |
109,556,970 (GRCm39) |
missense |
probably damaging |
1.00 |
R1935:Rtl1
|
UTSW |
12 |
109,558,354 (GRCm39) |
missense |
probably benign |
0.42 |
R2000:Rtl1
|
UTSW |
12 |
109,560,321 (GRCm39) |
missense |
probably damaging |
1.00 |
R2094:Rtl1
|
UTSW |
12 |
109,557,831 (GRCm39) |
missense |
unknown |
|
R2125:Rtl1
|
UTSW |
12 |
109,560,355 (GRCm39) |
missense |
possibly damaging |
0.64 |
R2166:Rtl1
|
UTSW |
12 |
109,556,988 (GRCm39) |
missense |
probably damaging |
1.00 |
R2247:Rtl1
|
UTSW |
12 |
109,561,413 (GRCm39) |
missense |
possibly damaging |
0.77 |
R2274:Rtl1
|
UTSW |
12 |
109,561,101 (GRCm39) |
missense |
unknown |
|
R2919:Rtl1
|
UTSW |
12 |
109,557,582 (GRCm39) |
missense |
unknown |
|
R2998:Rtl1
|
UTSW |
12 |
109,561,530 (GRCm39) |
missense |
probably damaging |
0.99 |
R4554:Rtl1
|
UTSW |
12 |
109,560,762 (GRCm39) |
missense |
possibly damaging |
0.53 |
R4566:Rtl1
|
UTSW |
12 |
109,559,293 (GRCm39) |
missense |
probably damaging |
1.00 |
R4887:Rtl1
|
UTSW |
12 |
109,558,138 (GRCm39) |
missense |
probably damaging |
0.96 |
R5399:Rtl1
|
UTSW |
12 |
109,556,736 (GRCm39) |
missense |
probably damaging |
1.00 |
R5512:Rtl1
|
UTSW |
12 |
109,557,805 (GRCm39) |
missense |
unknown |
|
R5616:Rtl1
|
UTSW |
12 |
109,559,173 (GRCm39) |
missense |
unknown |
|
R5644:Rtl1
|
UTSW |
12 |
109,558,013 (GRCm39) |
missense |
probably benign |
0.03 |
R5647:Rtl1
|
UTSW |
12 |
109,561,113 (GRCm39) |
missense |
unknown |
|
R5695:Rtl1
|
UTSW |
12 |
109,560,531 (GRCm39) |
missense |
probably damaging |
1.00 |
R5714:Rtl1
|
UTSW |
12 |
109,560,114 (GRCm39) |
missense |
probably damaging |
0.99 |
R5786:Rtl1
|
UTSW |
12 |
109,559,053 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5917:Rtl1
|
UTSW |
12 |
109,558,087 (GRCm39) |
missense |
possibly damaging |
0.82 |
R5948:Rtl1
|
UTSW |
12 |
109,557,033 (GRCm39) |
missense |
possibly damaging |
0.86 |
R6051:Rtl1
|
UTSW |
12 |
109,559,458 (GRCm39) |
missense |
probably damaging |
1.00 |
R6251:Rtl1
|
UTSW |
12 |
109,560,083 (GRCm39) |
missense |
probably benign |
0.16 |
R6342:Rtl1
|
UTSW |
12 |
109,558,735 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6433:Rtl1
|
UTSW |
12 |
109,561,630 (GRCm39) |
missense |
unknown |
|
R6815:Rtl1
|
UTSW |
12 |
109,560,937 (GRCm39) |
missense |
probably damaging |
0.98 |
R6968:Rtl1
|
UTSW |
12 |
109,561,113 (GRCm39) |
missense |
unknown |
|
R7002:Rtl1
|
UTSW |
12 |
109,560,381 (GRCm39) |
missense |
probably damaging |
0.97 |
R7020:Rtl1
|
UTSW |
12 |
109,558,749 (GRCm39) |
missense |
possibly damaging |
0.72 |
R7026:Rtl1
|
UTSW |
12 |
109,559,595 (GRCm39) |
missense |
probably damaging |
0.99 |
R7027:Rtl1
|
UTSW |
12 |
109,557,848 (GRCm39) |
small deletion |
probably benign |
|
R7196:Rtl1
|
UTSW |
12 |
109,559,221 (GRCm39) |
missense |
possibly damaging |
0.83 |
R7239:Rtl1
|
UTSW |
12 |
109,558,909 (GRCm39) |
missense |
probably benign |
0.05 |
R7476:Rtl1
|
UTSW |
12 |
109,557,539 (GRCm39) |
missense |
unknown |
|
R7589:Rtl1
|
UTSW |
12 |
109,560,279 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7655:Rtl1
|
UTSW |
12 |
109,557,442 (GRCm39) |
missense |
unknown |
|
R7656:Rtl1
|
UTSW |
12 |
109,557,442 (GRCm39) |
missense |
unknown |
|
R7657:Rtl1
|
UTSW |
12 |
109,561,818 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7720:Rtl1
|
UTSW |
12 |
109,560,864 (GRCm39) |
missense |
possibly damaging |
0.96 |
R7772:Rtl1
|
UTSW |
12 |
109,559,619 (GRCm39) |
missense |
probably damaging |
1.00 |
R7840:Rtl1
|
UTSW |
12 |
109,560,589 (GRCm39) |
missense |
probably benign |
0.08 |
R7890:Rtl1
|
UTSW |
12 |
109,559,251 (GRCm39) |
missense |
possibly damaging |
0.57 |
R7893:Rtl1
|
UTSW |
12 |
109,560,355 (GRCm39) |
missense |
possibly damaging |
0.64 |
R7894:Rtl1
|
UTSW |
12 |
109,561,031 (GRCm39) |
missense |
possibly damaging |
0.70 |
R7909:Rtl1
|
UTSW |
12 |
109,558,914 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7909:Rtl1
|
UTSW |
12 |
109,556,611 (GRCm39) |
missense |
unknown |
|
R7986:Rtl1
|
UTSW |
12 |
109,558,492 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8007:Rtl1
|
UTSW |
12 |
109,558,060 (GRCm39) |
missense |
possibly damaging |
0.86 |
R8146:Rtl1
|
UTSW |
12 |
109,557,145 (GRCm39) |
missense |
probably benign |
0.01 |
R8193:Rtl1
|
UTSW |
12 |
109,558,650 (GRCm39) |
missense |
probably benign |
0.03 |
R8263:Rtl1
|
UTSW |
12 |
109,560,180 (GRCm39) |
missense |
probably damaging |
0.99 |
R8273:Rtl1
|
UTSW |
12 |
109,559,149 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8512:Rtl1
|
UTSW |
12 |
109,561,051 (GRCm39) |
missense |
unknown |
|
R8514:Rtl1
|
UTSW |
12 |
109,560,307 (GRCm39) |
missense |
possibly damaging |
0.52 |
R8748:Rtl1
|
UTSW |
12 |
109,561,492 (GRCm39) |
missense |
probably benign |
0.39 |
R9036:Rtl1
|
UTSW |
12 |
109,559,691 (GRCm39) |
missense |
probably benign |
0.03 |
R9104:Rtl1
|
UTSW |
12 |
109,560,718 (GRCm39) |
missense |
probably benign |
0.21 |
R9151:Rtl1
|
UTSW |
12 |
109,560,007 (GRCm39) |
missense |
|
|
R9238:Rtl1
|
UTSW |
12 |
109,561,017 (GRCm39) |
missense |
possibly damaging |
0.72 |
R9292:Rtl1
|
UTSW |
12 |
109,556,673 (GRCm39) |
missense |
possibly damaging |
0.91 |
R9329:Rtl1
|
UTSW |
12 |
109,556,673 (GRCm39) |
missense |
possibly damaging |
0.91 |
R9332:Rtl1
|
UTSW |
12 |
109,557,291 (GRCm39) |
missense |
probably benign |
0.01 |
R9342:Rtl1
|
UTSW |
12 |
109,558,884 (GRCm39) |
missense |
probably damaging |
1.00 |
R9350:Rtl1
|
UTSW |
12 |
109,557,226 (GRCm39) |
nonsense |
probably null |
|
R9446:Rtl1
|
UTSW |
12 |
109,556,604 (GRCm39) |
makesense |
probably null |
|
R9523:Rtl1
|
UTSW |
12 |
109,561,113 (GRCm39) |
missense |
unknown |
|
R9524:Rtl1
|
UTSW |
12 |
109,556,973 (GRCm39) |
missense |
probably damaging |
1.00 |
R9535:Rtl1
|
UTSW |
12 |
109,561,698 (GRCm39) |
missense |
unknown |
|
R9535:Rtl1
|
UTSW |
12 |
109,557,171 (GRCm39) |
missense |
probably damaging |
1.00 |
R9564:Rtl1
|
UTSW |
12 |
109,556,713 (GRCm39) |
missense |
probably benign |
0.19 |
R9615:Rtl1
|
UTSW |
12 |
109,556,835 (GRCm39) |
missense |
possibly damaging |
0.65 |
R9661:Rtl1
|
UTSW |
12 |
109,557,346 (GRCm39) |
missense |
possibly damaging |
0.79 |
R9674:Rtl1
|
UTSW |
12 |
109,559,024 (GRCm39) |
missense |
possibly damaging |
0.50 |
R9720:Rtl1
|
UTSW |
12 |
109,559,882 (GRCm39) |
missense |
possibly damaging |
0.50 |
Z1088:Rtl1
|
UTSW |
12 |
109,558,753 (GRCm39) |
missense |
probably benign |
0.02 |
|