Other mutations in this stock |
Total: 58 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4931406B18Rik |
A |
T |
7: 43,147,623 (GRCm39) |
D249E |
probably damaging |
Het |
Acacb |
A |
C |
5: 114,347,812 (GRCm39) |
|
probably null |
Het |
Adnp |
A |
G |
2: 168,025,918 (GRCm39) |
V459A |
probably damaging |
Het |
Arid3b |
T |
C |
9: 57,704,037 (GRCm39) |
K304E |
probably damaging |
Het |
Ash1l |
G |
T |
3: 88,977,816 (GRCm39) |
R2713L |
probably damaging |
Het |
Bmpr1a |
A |
C |
14: 34,136,720 (GRCm39) |
D490E |
probably benign |
Het |
Cacna1g |
A |
T |
11: 94,323,393 (GRCm39) |
C1270* |
probably null |
Het |
Cep295nl |
G |
T |
11: 118,223,866 (GRCm39) |
P326Q |
probably damaging |
Het |
Cfap100 |
T |
C |
6: 90,383,043 (GRCm39) |
I377V |
unknown |
Het |
Creb1 |
C |
T |
1: 64,615,436 (GRCm39) |
Q223* |
probably null |
Het |
Ctsc |
G |
A |
7: 87,958,767 (GRCm39) |
G349D |
probably damaging |
Het |
Ddx41 |
G |
A |
13: 55,681,769 (GRCm39) |
R311* |
probably null |
Het |
Dpcd |
A |
G |
19: 45,565,473 (GRCm39) |
Q149R |
probably benign |
Het |
Dse |
T |
A |
10: 34,060,144 (GRCm39) |
|
probably benign |
Het |
Dync2i1 |
A |
G |
12: 116,226,205 (GRCm39) |
|
probably benign |
Het |
Eef2k |
C |
T |
7: 120,488,488 (GRCm39) |
H458Y |
probably benign |
Het |
Gipr |
A |
T |
7: 18,897,538 (GRCm39) |
V90E |
probably damaging |
Het |
Gm14412 |
A |
T |
2: 177,009,189 (GRCm39) |
D22E |
probably damaging |
Het |
Gm21886 |
A |
T |
18: 80,132,950 (GRCm39) |
C69* |
probably null |
Het |
Gm5114 |
G |
A |
7: 39,058,390 (GRCm39) |
L410F |
probably benign |
Het |
Gmip |
T |
A |
8: 70,269,118 (GRCm39) |
|
probably null |
Het |
Gtf2f1 |
T |
C |
17: 57,314,101 (GRCm39) |
T128A |
possibly damaging |
Het |
Hnrnpr |
A |
G |
4: 136,059,886 (GRCm39) |
E330G |
possibly damaging |
Het |
Hoxd9 |
T |
A |
2: 74,528,718 (GRCm39) |
W107R |
probably damaging |
Het |
Iars1 |
T |
C |
13: 49,876,554 (GRCm39) |
|
probably null |
Het |
Idh2 |
TCCCAGGGCC |
TCC |
7: 79,748,079 (GRCm39) |
|
probably null |
Het |
Ifi213 |
G |
T |
1: 173,421,529 (GRCm39) |
P120Q |
probably damaging |
Het |
Il6 |
A |
T |
5: 30,219,906 (GRCm39) |
Q94L |
probably benign |
Het |
Kcnab1 |
A |
G |
3: 65,226,908 (GRCm39) |
S196G |
probably benign |
Het |
Kcnv1 |
C |
T |
15: 44,976,604 (GRCm39) |
V228I |
probably benign |
Het |
Lars2 |
A |
G |
9: 123,284,028 (GRCm39) |
T739A |
possibly damaging |
Het |
Med13 |
T |
C |
11: 86,210,661 (GRCm39) |
S494G |
probably benign |
Het |
Mtrf1 |
GCCTTC |
GC |
14: 79,660,931 (GRCm39) |
|
probably null |
Het |
Myh9 |
T |
G |
15: 77,650,024 (GRCm39) |
Q1646P |
probably damaging |
Het |
Nif3l1 |
T |
A |
1: 58,489,625 (GRCm39) |
S171R |
probably benign |
Het |
Or13n4 |
A |
G |
7: 106,422,777 (GRCm39) |
*319Q |
probably null |
Het |
Or1e1c |
A |
G |
11: 73,266,201 (GRCm39) |
I212V |
probably benign |
Het |
Or1r1 |
A |
G |
11: 73,874,603 (GRCm39) |
V277A |
probably benign |
Het |
Or51f23 |
A |
G |
7: 102,452,765 (GRCm39) |
T27A |
probably benign |
Het |
Or6c5b |
T |
C |
10: 129,245,649 (GRCm39) |
V138A |
probably benign |
Het |
Or8c8 |
T |
C |
9: 38,164,719 (GRCm39) |
M2T |
probably benign |
Het |
Pak5 |
A |
T |
2: 135,958,684 (GRCm39) |
S135T |
possibly damaging |
Het |
Prr29 |
A |
T |
11: 106,265,684 (GRCm39) |
M1L |
probably damaging |
Het |
Ptpn13 |
T |
A |
5: 103,742,502 (GRCm39) |
V2407E |
probably damaging |
Het |
Ralgapa1 |
T |
A |
12: 55,741,978 (GRCm39) |
H1310L |
probably damaging |
Het |
Raph1 |
T |
C |
1: 60,538,767 (GRCm39) |
S393G |
unknown |
Het |
Rgl2 |
T |
C |
17: 34,153,964 (GRCm39) |
F457L |
possibly damaging |
Het |
Ror2 |
A |
G |
13: 53,272,756 (GRCm39) |
I303T |
possibly damaging |
Het |
Runx2 |
G |
A |
17: 45,125,079 (GRCm39) |
P80L |
probably damaging |
Het |
Scn10a |
C |
T |
9: 119,447,921 (GRCm39) |
D1378N |
probably damaging |
Het |
Serpinc1 |
T |
A |
1: 160,821,188 (GRCm39) |
C91S |
probably benign |
Het |
Sorbs1 |
G |
C |
19: 40,365,244 (GRCm39) |
R180G |
probably benign |
Het |
Spata31d1e |
T |
C |
13: 59,889,790 (GRCm39) |
I677V |
probably benign |
Het |
Tada1 |
T |
A |
1: 166,216,217 (GRCm39) |
C139* |
probably null |
Het |
Tbr1 |
T |
A |
2: 61,636,386 (GRCm39) |
V254E |
probably damaging |
Het |
Timd4 |
A |
T |
11: 46,734,016 (GRCm39) |
I340F |
probably benign |
Het |
Tubb2a |
T |
C |
13: 34,258,515 (GRCm39) |
Y425C |
probably damaging |
Het |
Zfp292 |
A |
T |
4: 34,819,476 (GRCm39) |
M287K |
probably damaging |
Het |
|
Other mutations in Or5b113 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00936:Or5b113
|
APN |
19 |
13,341,988 (GRCm39) |
utr 5 prime |
probably benign |
|
IGL01109:Or5b113
|
APN |
19 |
13,342,063 (GRCm39) |
missense |
probably benign |
|
IGL01939:Or5b113
|
APN |
19 |
13,342,807 (GRCm39) |
missense |
probably benign |
0.14 |
IGL02188:Or5b113
|
APN |
19 |
13,342,643 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02188:Or5b113
|
APN |
19 |
13,342,396 (GRCm39) |
missense |
probably benign |
0.39 |
IGL03223:Or5b113
|
APN |
19 |
13,342,645 (GRCm39) |
missense |
probably benign |
|
R0456:Or5b113
|
UTSW |
19 |
13,342,102 (GRCm39) |
missense |
probably damaging |
0.98 |
R1066:Or5b113
|
UTSW |
19 |
13,342,451 (GRCm39) |
missense |
probably benign |
|
R1189:Or5b113
|
UTSW |
19 |
13,342,543 (GRCm39) |
missense |
probably benign |
0.03 |
R1668:Or5b113
|
UTSW |
19 |
13,342,234 (GRCm39) |
missense |
probably benign |
0.00 |
R1754:Or5b113
|
UTSW |
19 |
13,342,717 (GRCm39) |
missense |
probably damaging |
1.00 |
R1860:Or5b113
|
UTSW |
19 |
13,342,705 (GRCm39) |
missense |
possibly damaging |
0.80 |
R1861:Or5b113
|
UTSW |
19 |
13,342,705 (GRCm39) |
missense |
possibly damaging |
0.80 |
R2181:Or5b113
|
UTSW |
19 |
13,342,438 (GRCm39) |
missense |
probably benign |
0.08 |
R2219:Or5b113
|
UTSW |
19 |
13,342,901 (GRCm39) |
missense |
possibly damaging |
0.88 |
R2516:Or5b113
|
UTSW |
19 |
13,342,557 (GRCm39) |
nonsense |
probably null |
|
R4757:Or5b113
|
UTSW |
19 |
13,342,810 (GRCm39) |
missense |
probably benign |
0.23 |
R5206:Or5b113
|
UTSW |
19 |
13,342,429 (GRCm39) |
missense |
possibly damaging |
0.91 |
R5376:Or5b113
|
UTSW |
19 |
13,342,762 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5647:Or5b113
|
UTSW |
19 |
13,342,541 (GRCm39) |
missense |
probably damaging |
1.00 |
R5724:Or5b113
|
UTSW |
19 |
13,342,515 (GRCm39) |
missense |
possibly damaging |
0.62 |
R5741:Or5b113
|
UTSW |
19 |
13,342,847 (GRCm39) |
missense |
probably damaging |
0.97 |
R5906:Or5b113
|
UTSW |
19 |
13,342,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R6636:Or5b113
|
UTSW |
19 |
13,342,589 (GRCm39) |
missense |
probably benign |
0.06 |
R6637:Or5b113
|
UTSW |
19 |
13,342,589 (GRCm39) |
missense |
probably benign |
0.06 |
R7000:Or5b113
|
UTSW |
19 |
13,341,987 (GRCm39) |
start gained |
probably benign |
|
R7325:Or5b113
|
UTSW |
19 |
13,342,001 (GRCm39) |
missense |
probably benign |
0.00 |
R7773:Or5b113
|
UTSW |
19 |
13,342,598 (GRCm39) |
missense |
probably benign |
0.07 |
R7828:Or5b113
|
UTSW |
19 |
13,342,510 (GRCm39) |
missense |
probably benign |
0.10 |
R9081:Or5b113
|
UTSW |
19 |
13,342,019 (GRCm39) |
missense |
probably benign |
0.12 |
R9135:Or5b113
|
UTSW |
19 |
13,342,755 (GRCm39) |
missense |
possibly damaging |
0.46 |
R9151:Or5b113
|
UTSW |
19 |
13,342,222 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9470:Or5b113
|
UTSW |
19 |
13,342,115 (GRCm39) |
missense |
probably damaging |
1.00 |
R9792:Or5b113
|
UTSW |
19 |
13,342,514 (GRCm39) |
missense |
probably damaging |
0.99 |
R9793:Or5b113
|
UTSW |
19 |
13,342,514 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1176:Or5b113
|
UTSW |
19 |
13,342,280 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Or5b113
|
UTSW |
19 |
13,342,279 (GRCm39) |
missense |
probably damaging |
1.00 |
|