Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A130010J15Rik |
A |
G |
1: 192,857,154 (GRCm39) |
I169V |
probably benign |
Het |
Arrdc5 |
A |
G |
17: 56,604,856 (GRCm39) |
S144P |
probably benign |
Het |
Astn1 |
A |
G |
1: 158,495,179 (GRCm39) |
M92V |
probably benign |
Het |
Atg5 |
A |
G |
10: 44,195,544 (GRCm39) |
I189M |
probably damaging |
Het |
Atmin |
A |
G |
8: 117,684,277 (GRCm39) |
T646A |
probably damaging |
Het |
Atp1a2 |
G |
A |
1: 172,115,000 (GRCm39) |
R262W |
probably damaging |
Het |
Atp6v1g2 |
A |
G |
17: 35,455,785 (GRCm39) |
K16E |
probably damaging |
Het |
Bex6 |
G |
A |
16: 32,005,278 (GRCm39) |
E29K |
possibly damaging |
Het |
Casd1 |
A |
G |
6: 4,608,705 (GRCm39) |
Y101C |
probably damaging |
Het |
Ccdc168 |
A |
C |
1: 44,098,890 (GRCm39) |
I736S |
probably benign |
Het |
Cdx1 |
T |
C |
18: 61,168,984 (GRCm39) |
D70G |
possibly damaging |
Het |
Cebpz |
T |
C |
17: 79,242,983 (GRCm39) |
T224A |
probably benign |
Het |
Cep170b |
T |
C |
12: 112,702,164 (GRCm39) |
V319A |
possibly damaging |
Het |
Chrna2 |
C |
T |
14: 66,386,912 (GRCm39) |
R353W |
possibly damaging |
Het |
Chst5 |
A |
T |
8: 112,617,176 (GRCm39) |
V148E |
probably benign |
Het |
Clhc1 |
T |
A |
11: 29,507,771 (GRCm39) |
W162R |
probably benign |
Het |
Csmd1 |
T |
A |
8: 16,129,992 (GRCm39) |
Q1710L |
probably damaging |
Het |
Ddb1 |
A |
C |
19: 10,590,300 (GRCm39) |
M276L |
probably benign |
Het |
Dot1l |
C |
T |
10: 80,621,712 (GRCm39) |
R455C |
probably damaging |
Het |
Dync2h1 |
A |
G |
9: 7,148,735 (GRCm39) |
V903A |
probably benign |
Het |
Eno1b |
T |
C |
18: 48,180,542 (GRCm39) |
V240A |
possibly damaging |
Het |
Erich1 |
T |
G |
8: 14,140,527 (GRCm39) |
|
probably benign |
Het |
Ermp1 |
A |
C |
19: 29,617,328 (GRCm39) |
S227A |
probably benign |
Het |
Etv1 |
C |
A |
12: 38,885,115 (GRCm39) |
P143Q |
probably null |
Het |
Gimap8 |
A |
T |
6: 48,627,502 (GRCm39) |
I159F |
probably benign |
Het |
Gpr4 |
G |
A |
7: 18,956,503 (GRCm39) |
V142M |
possibly damaging |
Het |
Gucy1a1 |
C |
T |
3: 82,020,639 (GRCm39) |
C86Y |
probably benign |
Het |
Ifngr2 |
T |
G |
16: 91,358,667 (GRCm39) |
|
probably null |
Het |
Insrr |
A |
T |
3: 87,710,488 (GRCm39) |
N398I |
probably damaging |
Het |
Iws1 |
A |
G |
18: 32,217,719 (GRCm39) |
E441G |
probably damaging |
Het |
Larp7-ps |
A |
G |
4: 92,079,893 (GRCm39) |
S32P |
probably damaging |
Het |
Megf10 |
A |
T |
18: 57,414,785 (GRCm39) |
K732* |
probably null |
Het |
Mprip |
T |
A |
11: 59,640,334 (GRCm39) |
|
probably benign |
Het |
Mrgprb8 |
T |
C |
7: 48,038,953 (GRCm39) |
V208A |
probably benign |
Het |
Msc |
G |
C |
1: 14,825,908 (GRCm39) |
P22R |
probably benign |
Het |
Opcml |
G |
A |
9: 28,812,886 (GRCm39) |
E193K |
probably damaging |
Het |
Or4k15b |
A |
T |
14: 50,272,171 (GRCm39) |
S230T |
probably damaging |
Het |
Oxsr1 |
A |
C |
9: 119,123,560 (GRCm39) |
H71Q |
probably benign |
Het |
Pkp2 |
T |
A |
16: 16,064,831 (GRCm39) |
W452R |
probably damaging |
Het |
Prrc2b |
C |
T |
2: 32,072,582 (GRCm39) |
T20I |
probably damaging |
Het |
Rasgrp3 |
T |
C |
17: 75,810,136 (GRCm39) |
S279P |
probably damaging |
Het |
Serpina3m |
G |
T |
12: 104,355,529 (GRCm39) |
K65N |
probably benign |
Het |
Serpine2 |
A |
G |
1: 79,788,411 (GRCm39) |
V182A |
probably damaging |
Het |
Slc10a1 |
A |
G |
12: 81,002,822 (GRCm39) |
V272A |
possibly damaging |
Het |
Slc25a29 |
A |
T |
12: 108,793,358 (GRCm39) |
N73K |
probably damaging |
Het |
Slit1 |
G |
A |
19: 41,594,819 (GRCm39) |
R1184W |
probably damaging |
Het |
Srrm2 |
T |
C |
17: 24,031,403 (GRCm39) |
|
probably benign |
Het |
Stk11ip |
A |
G |
1: 75,502,165 (GRCm39) |
|
probably benign |
Het |
Tcerg1 |
A |
G |
18: 42,697,210 (GRCm39) |
K767R |
possibly damaging |
Het |
Tmem82 |
T |
C |
4: 141,343,598 (GRCm39) |
K224R |
probably benign |
Het |
Tmprss11g |
A |
G |
5: 86,647,415 (GRCm39) |
L41S |
probably damaging |
Het |
Trim42 |
T |
C |
9: 97,248,150 (GRCm39) |
N182S |
probably benign |
Het |
Ttn |
T |
C |
2: 76,660,432 (GRCm39) |
T7430A |
probably benign |
Het |
Wwp1 |
T |
C |
4: 19,650,390 (GRCm39) |
T259A |
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 |
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 |
R7312:Rtl1
|
UTSW |
12 |
109,561,672 (GRCm39) |
missense |
unknown |
|
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 |
|