Other mutations in this stock |
Total: 87 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A230072I06Rik |
C |
T |
8: 12,329,899 (GRCm39) |
S118L |
unknown |
Het |
Adprs |
A |
G |
4: 126,211,947 (GRCm39) |
Y122H |
probably damaging |
Het |
Ankrd52 |
T |
C |
10: 128,222,007 (GRCm39) |
S544P |
probably benign |
Het |
Aopep |
A |
G |
13: 63,338,298 (GRCm39) |
N558S |
probably benign |
Het |
Arhgef7 |
A |
G |
8: 11,850,503 (GRCm39) |
E111G |
probably damaging |
Het |
Atp11a |
A |
G |
8: 12,896,054 (GRCm39) |
M755V |
probably benign |
Het |
Atp2a2 |
A |
G |
5: 122,629,778 (GRCm39) |
I97T |
probably damaging |
Het |
Bmp3 |
G |
A |
5: 99,027,768 (GRCm39) |
D463N |
possibly damaging |
Het |
Cacna2d4 |
T |
C |
6: 119,255,230 (GRCm39) |
|
probably benign |
Het |
Ccdc28a |
G |
A |
10: 18,106,188 (GRCm39) |
S46F |
possibly damaging |
Het |
Ccdc40 |
G |
A |
11: 119,155,125 (GRCm39) |
G1122S |
probably benign |
Het |
Cenpw |
T |
G |
10: 30,076,455 (GRCm39) |
T8P |
probably benign |
Het |
Cfap44 |
G |
C |
16: 44,253,785 (GRCm39) |
G893R |
possibly damaging |
Het |
Cimap3 |
A |
T |
3: 105,906,886 (GRCm39) |
M171K |
possibly damaging |
Het |
Cops7a |
A |
T |
6: 124,938,323 (GRCm39) |
C110S |
probably damaging |
Het |
Cstl1 |
A |
G |
2: 148,597,245 (GRCm39) |
N134S |
probably damaging |
Het |
Cyp2s1 |
G |
T |
7: 25,511,114 (GRCm39) |
|
probably null |
Het |
Dio2 |
T |
A |
12: 90,696,617 (GRCm39) |
N124Y |
probably damaging |
Het |
Efr3a |
G |
T |
15: 65,717,830 (GRCm39) |
V337F |
possibly damaging |
Het |
Eva1b |
A |
C |
4: 126,043,446 (GRCm39) |
H162P |
probably damaging |
Het |
Exoc5 |
C |
T |
14: 49,273,493 (GRCm39) |
E301K |
probably damaging |
Het |
F13b |
G |
A |
1: 139,435,941 (GRCm39) |
S249N |
probably damaging |
Het |
Fam120b |
C |
T |
17: 15,646,446 (GRCm39) |
|
probably benign |
Het |
Gbf1 |
T |
C |
19: 46,250,231 (GRCm39) |
L396S |
probably damaging |
Het |
Gck |
T |
A |
11: 5,859,139 (GRCm39) |
K143* |
probably null |
Het |
Gck |
C |
A |
11: 5,860,370 (GRCm39) |
V91L |
probably damaging |
Het |
Glt8d2 |
T |
C |
10: 82,496,644 (GRCm39) |
N138S |
probably damaging |
Het |
Gm4884 |
T |
C |
7: 40,692,387 (GRCm39) |
F119L |
probably benign |
Het |
Igsf11 |
T |
C |
16: 38,829,240 (GRCm39) |
S45P |
probably damaging |
Het |
Iho1 |
T |
C |
9: 108,289,695 (GRCm39) |
T176A |
probably damaging |
Het |
Il10 |
G |
A |
1: 130,950,271 (GRCm39) |
V142M |
probably damaging |
Het |
Insc |
A |
T |
7: 114,368,237 (GRCm39) |
H9L |
probably damaging |
Het |
Iqsec1 |
G |
T |
6: 90,786,740 (GRCm39) |
|
probably benign |
Het |
Katnb1 |
A |
G |
8: 95,825,050 (GRCm39) |
S611G |
possibly damaging |
Het |
Kcnb1 |
A |
G |
2: 166,947,459 (GRCm39) |
I463T |
possibly damaging |
Het |
Lao1 |
A |
G |
4: 118,821,399 (GRCm39) |
N90S |
probably benign |
Het |
Med16 |
T |
A |
10: 79,732,635 (GRCm39) |
M710L |
probably benign |
Het |
Mroh2a |
G |
C |
1: 88,185,524 (GRCm39) |
E1510D |
probably damaging |
Het |
Mtus1 |
G |
A |
8: 41,469,233 (GRCm39) |
|
probably benign |
Het |
Mybpc3 |
A |
G |
2: 90,950,682 (GRCm39) |
|
probably benign |
Het |
Ndor1 |
C |
T |
2: 25,138,366 (GRCm39) |
V405M |
possibly damaging |
Het |
Nell2 |
A |
G |
15: 95,330,782 (GRCm39) |
V213A |
probably benign |
Het |
Nme8 |
T |
C |
13: 19,862,018 (GRCm39) |
I204V |
probably benign |
Het |
Nup133 |
A |
T |
8: 124,656,082 (GRCm39) |
N466K |
probably benign |
Het |
Nxt1 |
A |
G |
2: 148,517,390 (GRCm39) |
T44A |
probably benign |
Het |
Or14c46 |
T |
C |
7: 85,918,187 (GRCm39) |
E270G |
probably benign |
Het |
Or2ag15 |
A |
T |
7: 106,340,832 (GRCm39) |
I103N |
probably benign |
Het |
Or2y12 |
C |
T |
11: 49,426,401 (GRCm39) |
L130F |
probably benign |
Het |
Or4e1 |
T |
C |
14: 52,700,669 (GRCm39) |
T239A |
probably damaging |
Het |
Or4f7 |
A |
T |
2: 111,644,699 (GRCm39) |
I124K |
possibly damaging |
Het |
Or7e168 |
C |
T |
9: 19,720,165 (GRCm39) |
L184F |
probably damaging |
Het |
Pced1a |
T |
C |
2: 130,263,827 (GRCm39) |
K275R |
probably benign |
Het |
Pdcd11 |
A |
G |
19: 47,099,398 (GRCm39) |
|
probably null |
Het |
Phldb2 |
A |
C |
16: 45,591,029 (GRCm39) |
|
probably benign |
Het |
Piwil1 |
C |
A |
5: 128,824,387 (GRCm39) |
S490Y |
probably damaging |
Het |
Plekhh3 |
T |
C |
11: 101,054,501 (GRCm39) |
|
probably benign |
Het |
Ppargc1b |
A |
T |
18: 61,449,034 (GRCm39) |
|
probably benign |
Het |
Psg19 |
C |
T |
7: 18,530,942 (GRCm39) |
V71I |
possibly damaging |
Het |
Ptk6 |
T |
C |
2: 180,838,724 (GRCm39) |
|
probably benign |
Het |
Pus7 |
A |
G |
5: 23,983,090 (GRCm39) |
S126P |
probably damaging |
Het |
Rab6b |
T |
A |
9: 103,017,576 (GRCm39) |
|
probably null |
Het |
Ranbp3 |
G |
A |
17: 57,016,272 (GRCm39) |
R347Q |
possibly damaging |
Het |
Sanbr |
A |
T |
11: 23,570,214 (GRCm39) |
|
probably benign |
Het |
Sbf1 |
A |
T |
15: 89,186,701 (GRCm39) |
L866Q |
probably damaging |
Het |
Slc25a34 |
A |
G |
4: 141,349,663 (GRCm39) |
V164A |
possibly damaging |
Het |
Smg1 |
A |
G |
7: 117,751,898 (GRCm39) |
|
probably null |
Het |
Spin1 |
G |
T |
13: 51,303,048 (GRCm39) |
V214L |
probably benign |
Het |
Spmip2 |
A |
T |
3: 79,313,142 (GRCm39) |
Y72F |
probably damaging |
Het |
Sptbn1 |
T |
C |
11: 30,092,289 (GRCm39) |
N492S |
probably benign |
Het |
Stk-ps2 |
A |
G |
1: 46,068,955 (GRCm39) |
|
noncoding transcript |
Het |
Taar7f |
T |
C |
10: 23,926,312 (GRCm39) |
I302T |
probably benign |
Het |
Tdrd1 |
C |
A |
19: 56,831,630 (GRCm39) |
H340Q |
probably benign |
Het |
Thumpd3 |
A |
G |
6: 113,044,762 (GRCm39) |
D498G |
probably benign |
Het |
Tpgs2 |
A |
G |
18: 25,282,242 (GRCm39) |
L103P |
probably damaging |
Het |
Trip10 |
A |
G |
17: 57,568,633 (GRCm39) |
|
probably null |
Het |
Trip6 |
A |
T |
5: 137,310,436 (GRCm39) |
H269Q |
probably benign |
Het |
Trmt12 |
T |
C |
15: 58,744,743 (GRCm39) |
V47A |
possibly damaging |
Het |
Trpm7 |
A |
T |
2: 126,654,691 (GRCm39) |
S1416T |
probably benign |
Het |
Tsks |
G |
A |
7: 44,603,883 (GRCm39) |
A438T |
probably benign |
Het |
Ttn |
T |
C |
2: 76,727,630 (GRCm39) |
|
probably benign |
Het |
Twf2 |
G |
A |
9: 106,090,155 (GRCm39) |
V136M |
possibly damaging |
Het |
Uty |
A |
C |
Y: 1,197,223 (GRCm39) |
Y115D |
probably damaging |
Het |
Vcan |
A |
G |
13: 89,839,380 (GRCm39) |
S2055P |
probably damaging |
Het |
Yes1 |
A |
G |
5: 32,842,039 (GRCm39) |
Q521R |
possibly damaging |
Het |
Zfp114 |
A |
T |
7: 23,880,685 (GRCm39) |
T344S |
possibly damaging |
Het |
Zfp661 |
A |
T |
2: 127,420,532 (GRCm39) |
V89D |
possibly damaging |
Het |
Zfp91 |
A |
T |
19: 12,747,834 (GRCm39) |
Y430N |
probably damaging |
Het |
|
Other mutations in Ecel1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01161:Ecel1
|
APN |
1 |
87,080,915 (GRCm39) |
missense |
possibly damaging |
0.84 |
IGL01431:Ecel1
|
APN |
1 |
87,079,226 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01992:Ecel1
|
APN |
1 |
87,077,577 (GRCm39) |
splice site |
probably benign |
|
IGL02040:Ecel1
|
APN |
1 |
87,082,645 (GRCm39) |
missense |
probably benign |
0.32 |
IGL02230:Ecel1
|
APN |
1 |
87,079,916 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02801:Ecel1
|
APN |
1 |
87,079,725 (GRCm39) |
missense |
probably damaging |
1.00 |
Capulin
|
UTSW |
1 |
87,081,023 (GRCm39) |
missense |
probably damaging |
0.99 |
R1723:Ecel1
|
UTSW |
1 |
87,082,143 (GRCm39) |
missense |
probably benign |
0.37 |
R2118:Ecel1
|
UTSW |
1 |
87,075,997 (GRCm39) |
missense |
probably damaging |
1.00 |
R2119:Ecel1
|
UTSW |
1 |
87,075,997 (GRCm39) |
missense |
probably damaging |
1.00 |
R2120:Ecel1
|
UTSW |
1 |
87,075,997 (GRCm39) |
missense |
probably damaging |
1.00 |
R2122:Ecel1
|
UTSW |
1 |
87,075,997 (GRCm39) |
missense |
probably damaging |
1.00 |
R3815:Ecel1
|
UTSW |
1 |
87,080,622 (GRCm39) |
missense |
probably damaging |
0.97 |
R3836:Ecel1
|
UTSW |
1 |
87,078,378 (GRCm39) |
missense |
probably damaging |
1.00 |
R4211:Ecel1
|
UTSW |
1 |
87,079,872 (GRCm39) |
missense |
probably damaging |
1.00 |
R4685:Ecel1
|
UTSW |
1 |
87,080,668 (GRCm39) |
splice site |
probably null |
|
R4841:Ecel1
|
UTSW |
1 |
87,081,023 (GRCm39) |
missense |
probably damaging |
0.99 |
R4842:Ecel1
|
UTSW |
1 |
87,081,023 (GRCm39) |
missense |
probably damaging |
0.99 |
R4888:Ecel1
|
UTSW |
1 |
87,076,449 (GRCm39) |
splice site |
probably benign |
|
R4976:Ecel1
|
UTSW |
1 |
87,078,861 (GRCm39) |
missense |
probably benign |
0.17 |
R5032:Ecel1
|
UTSW |
1 |
87,081,975 (GRCm39) |
missense |
probably damaging |
0.97 |
R5119:Ecel1
|
UTSW |
1 |
87,078,861 (GRCm39) |
missense |
probably benign |
0.17 |
R5393:Ecel1
|
UTSW |
1 |
87,080,598 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5798:Ecel1
|
UTSW |
1 |
87,079,205 (GRCm39) |
missense |
probably damaging |
1.00 |
R5862:Ecel1
|
UTSW |
1 |
87,077,318 (GRCm39) |
missense |
probably benign |
0.19 |
R5874:Ecel1
|
UTSW |
1 |
87,075,731 (GRCm39) |
missense |
probably benign |
0.24 |
R6341:Ecel1
|
UTSW |
1 |
87,078,193 (GRCm39) |
splice site |
probably null |
|
R6351:Ecel1
|
UTSW |
1 |
87,077,231 (GRCm39) |
missense |
possibly damaging |
0.56 |
R6534:Ecel1
|
UTSW |
1 |
87,082,564 (GRCm39) |
missense |
probably benign |
0.13 |
R7405:Ecel1
|
UTSW |
1 |
87,081,238 (GRCm39) |
critical splice donor site |
probably null |
|
R7422:Ecel1
|
UTSW |
1 |
87,077,334 (GRCm39) |
missense |
probably damaging |
1.00 |
R7850:Ecel1
|
UTSW |
1 |
87,079,745 (GRCm39) |
missense |
probably damaging |
1.00 |
R7939:Ecel1
|
UTSW |
1 |
87,077,256 (GRCm39) |
missense |
probably benign |
0.19 |
R7950:Ecel1
|
UTSW |
1 |
87,075,991 (GRCm39) |
missense |
probably damaging |
0.98 |
R8022:Ecel1
|
UTSW |
1 |
87,081,052 (GRCm39) |
missense |
probably benign |
0.34 |
R8856:Ecel1
|
UTSW |
1 |
87,079,760 (GRCm39) |
missense |
probably damaging |
1.00 |
R8954:Ecel1
|
UTSW |
1 |
87,076,349 (GRCm39) |
nonsense |
probably null |
|
R8967:Ecel1
|
UTSW |
1 |
87,078,862 (GRCm39) |
missense |
probably damaging |
0.98 |
R9248:Ecel1
|
UTSW |
1 |
87,081,112 (GRCm39) |
missense |
probably benign |
0.00 |
R9395:Ecel1
|
UTSW |
1 |
87,082,350 (GRCm39) |
missense |
probably damaging |
0.99 |
R9487:Ecel1
|
UTSW |
1 |
87,075,716 (GRCm39) |
missense |
probably damaging |
1.00 |
R9620:Ecel1
|
UTSW |
1 |
87,080,853 (GRCm39) |
missense |
possibly damaging |
0.65 |
R9676:Ecel1
|
UTSW |
1 |
87,079,743 (GRCm39) |
missense |
probably damaging |
1.00 |
R9694:Ecel1
|
UTSW |
1 |
87,080,853 (GRCm39) |
missense |
possibly damaging |
0.65 |
|