Other mutations in this stock |
Total: 70 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Agrn |
A |
G |
4: 156,253,675 (GRCm39) |
|
probably null |
Het |
Alb |
G |
C |
5: 90,615,214 (GRCm39) |
R242P |
probably damaging |
Het |
Anxa2r2 |
A |
T |
13: 120,488,529 (GRCm39) |
S7T |
possibly damaging |
Het |
Aph1b |
T |
C |
9: 66,691,823 (GRCm39) |
T195A |
probably benign |
Het |
Apoe |
G |
T |
7: 19,430,535 (GRCm39) |
R236S |
possibly damaging |
Het |
Arap3 |
G |
T |
18: 38,111,505 (GRCm39) |
T1137K |
probably damaging |
Het |
Arhgap45 |
C |
T |
10: 79,864,672 (GRCm39) |
A908V |
probably benign |
Het |
Atp13a1 |
T |
C |
8: 70,258,209 (GRCm39) |
C965R |
probably damaging |
Het |
C7 |
A |
G |
15: 5,041,587 (GRCm39) |
Y440H |
probably damaging |
Het |
Cacna2d2 |
T |
C |
9: 107,401,397 (GRCm39) |
|
probably null |
Het |
Ddah2 |
C |
A |
17: 35,280,026 (GRCm39) |
R173S |
possibly damaging |
Het |
Dnajc11 |
T |
C |
4: 152,058,682 (GRCm39) |
Y337H |
probably damaging |
Het |
Dnajc25 |
A |
G |
4: 59,020,483 (GRCm39) |
K302R |
probably benign |
Het |
Dnajc6 |
A |
T |
4: 101,463,874 (GRCm39) |
Q209L |
probably damaging |
Het |
Drosha |
G |
A |
15: 12,859,522 (GRCm39) |
V577I |
probably benign |
Het |
Ebf2 |
G |
T |
14: 67,628,016 (GRCm39) |
|
probably null |
Het |
Epx |
A |
G |
11: 87,766,160 (GRCm39) |
|
probably null |
Het |
Fam107b |
A |
G |
2: 3,773,884 (GRCm39) |
N21S |
probably benign |
Het |
Fasn |
G |
A |
11: 120,707,154 (GRCm39) |
S857F |
probably damaging |
Het |
Fat1 |
A |
G |
8: 45,406,336 (GRCm39) |
N1029S |
probably damaging |
Het |
Gas8 |
A |
G |
8: 124,253,275 (GRCm39) |
I208V |
probably benign |
Het |
Gm3269 |
T |
C |
14: 16,026,209 (GRCm39) |
I88T |
probably benign |
Het |
Gm8005 |
C |
A |
14: 42,258,919 (GRCm39) |
L136F |
|
Het |
Grid2ip |
C |
A |
5: 143,368,393 (GRCm39) |
P743Q |
probably damaging |
Het |
H2-T15 |
A |
T |
17: 36,367,675 (GRCm39) |
V221D |
probably damaging |
Het |
Hbs1l |
C |
T |
10: 21,240,659 (GRCm39) |
T626I |
probably benign |
Het |
Hdac3 |
T |
A |
18: 38,087,972 (GRCm39) |
|
probably benign |
Het |
Hnrnpab |
T |
C |
11: 51,496,400 (GRCm39) |
Y94C |
probably damaging |
Het |
Homer2 |
T |
C |
7: 81,299,414 (GRCm39) |
D17G |
probably damaging |
Het |
Ikbke |
C |
T |
1: 131,199,569 (GRCm39) |
R308Q |
probably damaging |
Het |
Ints10 |
A |
G |
8: 69,277,771 (GRCm39) |
T682A |
possibly damaging |
Het |
Klhl3 |
G |
A |
13: 58,261,146 (GRCm39) |
|
probably benign |
Het |
Klk1b9 |
A |
T |
7: 43,445,514 (GRCm39) |
T235S |
probably benign |
Het |
Kmt2c |
T |
C |
5: 25,520,717 (GRCm39) |
T1798A |
probably benign |
Het |
Kri1 |
TTCCTCCTCCTCCTCCTCCTCCTCCTCCTC |
TTCCTCCTCCTCCTCCTCCTCCTCCTC |
9: 21,192,352 (GRCm39) |
|
probably benign |
Het |
Krtap4-6 |
T |
C |
11: 99,556,440 (GRCm39) |
I96V |
unknown |
Het |
Lef1 |
A |
C |
3: 130,994,003 (GRCm39) |
R354S |
probably damaging |
Het |
Lrp6 |
A |
T |
6: 134,488,208 (GRCm39) |
L296* |
probably null |
Het |
Maml2 |
T |
C |
9: 13,532,945 (GRCm39) |
Y720H |
|
Het |
Mmrn1 |
A |
G |
6: 60,954,490 (GRCm39) |
N924D |
probably benign |
Het |
Myh7b |
A |
G |
2: 155,474,156 (GRCm39) |
K1624E |
probably damaging |
Het |
Nos3 |
T |
A |
5: 24,588,610 (GRCm39) |
V1112D |
probably damaging |
Het |
Or2y14 |
T |
C |
11: 49,404,512 (GRCm39) |
F16L |
probably damaging |
Het |
Or4c111 |
C |
T |
2: 88,843,893 (GRCm39) |
V172I |
probably benign |
Het |
Or5an1b |
C |
A |
19: 12,299,651 (GRCm39) |
C180F |
probably damaging |
Het |
Or5w13 |
A |
G |
2: 87,523,704 (GRCm39) |
I174T |
probably damaging |
Het |
Or6c70 |
A |
T |
10: 129,710,346 (GRCm39) |
N93K |
probably damaging |
Het |
Phospho1 |
T |
C |
11: 95,721,645 (GRCm39) |
L105S |
probably damaging |
Het |
Prss35 |
T |
A |
9: 86,638,023 (GRCm39) |
N264K |
probably benign |
Het |
Ptpn13 |
A |
G |
5: 103,677,578 (GRCm39) |
D732G |
probably benign |
Het |
Rab18 |
A |
T |
18: 6,783,123 (GRCm39) |
T64S |
possibly damaging |
Het |
Rft1 |
A |
G |
14: 30,399,773 (GRCm39) |
Q319R |
probably benign |
Het |
Rgs7 |
T |
A |
1: 174,921,396 (GRCm39) |
M220L |
probably benign |
Het |
Rnf13 |
A |
G |
3: 57,671,772 (GRCm39) |
N28S |
probably benign |
Het |
Setd3 |
A |
T |
12: 108,078,548 (GRCm39) |
I311N |
probably damaging |
Het |
Setd5 |
G |
A |
6: 113,098,725 (GRCm39) |
R786H |
probably damaging |
Het |
Slc26a6 |
T |
C |
9: 108,733,143 (GRCm39) |
|
probably null |
Het |
Slc26a9 |
A |
T |
1: 131,691,634 (GRCm39) |
T626S |
probably benign |
Het |
Stambp |
A |
T |
6: 83,540,910 (GRCm39) |
|
probably null |
Het |
Stom |
A |
T |
2: 35,206,041 (GRCm39) |
N229K |
probably benign |
Het |
Tlr1 |
A |
T |
5: 65,084,130 (GRCm39) |
L149* |
probably null |
Het |
Trpc3 |
C |
A |
3: 36,692,677 (GRCm39) |
V772F |
probably benign |
Het |
Ube3a |
A |
G |
7: 58,893,102 (GRCm39) |
|
probably benign |
Het |
Ugt2b35 |
T |
A |
5: 87,149,369 (GRCm39) |
F207I |
probably damaging |
Het |
Usp53 |
A |
T |
3: 122,746,884 (GRCm39) |
D360E |
possibly damaging |
Het |
Vmn2r96 |
T |
G |
17: 18,793,832 (GRCm39) |
S59A |
probably benign |
Het |
Wdr70 |
A |
G |
15: 8,108,700 (GRCm39) |
C149R |
probably benign |
Het |
Wnt3 |
A |
G |
11: 103,703,290 (GRCm39) |
T258A |
possibly damaging |
Het |
Zfp729b |
T |
C |
13: 67,739,371 (GRCm39) |
T965A |
probably benign |
Het |
Zfp764l1 |
C |
T |
7: 126,992,496 (GRCm39) |
C38Y |
probably null |
Het |
|
Other mutations in Eqtn |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R0088:Eqtn
|
UTSW |
4 |
94,808,227 (GRCm39) |
missense |
probably damaging |
0.99 |
R0904:Eqtn
|
UTSW |
4 |
94,795,892 (GRCm39) |
missense |
probably benign |
0.18 |
R1605:Eqtn
|
UTSW |
4 |
94,816,587 (GRCm39) |
missense |
possibly damaging |
0.83 |
R2290:Eqtn
|
UTSW |
4 |
94,815,179 (GRCm39) |
small deletion |
probably benign |
|
R4072:Eqtn
|
UTSW |
4 |
94,808,199 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4073:Eqtn
|
UTSW |
4 |
94,808,199 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4074:Eqtn
|
UTSW |
4 |
94,808,199 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4075:Eqtn
|
UTSW |
4 |
94,808,199 (GRCm39) |
missense |
possibly damaging |
0.91 |
R5379:Eqtn
|
UTSW |
4 |
94,795,825 (GRCm39) |
missense |
probably damaging |
1.00 |
R5485:Eqtn
|
UTSW |
4 |
94,813,193 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5691:Eqtn
|
UTSW |
4 |
94,811,965 (GRCm39) |
critical splice acceptor site |
probably null |
|
R6252:Eqtn
|
UTSW |
4 |
94,796,006 (GRCm39) |
missense |
probably damaging |
0.98 |
R6707:Eqtn
|
UTSW |
4 |
94,796,056 (GRCm39) |
missense |
probably benign |
0.01 |
R6873:Eqtn
|
UTSW |
4 |
94,815,258 (GRCm39) |
missense |
probably damaging |
0.99 |
R7209:Eqtn
|
UTSW |
4 |
94,813,806 (GRCm39) |
missense |
probably damaging |
1.00 |
R7235:Eqtn
|
UTSW |
4 |
94,811,936 (GRCm39) |
missense |
probably damaging |
0.98 |
R7651:Eqtn
|
UTSW |
4 |
94,811,944 (GRCm39) |
missense |
possibly damaging |
0.52 |
R9566:Eqtn
|
UTSW |
4 |
94,813,185 (GRCm39) |
missense |
probably damaging |
0.98 |
X0063:Eqtn
|
UTSW |
4 |
94,816,555 (GRCm39) |
critical splice donor site |
probably null |
|
Z1177:Eqtn
|
UTSW |
4 |
94,795,788 (GRCm39) |
missense |
probably benign |
0.28 |
|