Other mutations in this stock |
Total: 76 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
5730409E04Rik |
T |
A |
4: 126,505,475 (GRCm39) |
M1K |
probably null |
Het |
5730507C01Rik |
A |
C |
12: 18,581,967 (GRCm39) |
R119S |
possibly damaging |
Het |
Abca1 |
T |
A |
4: 53,090,251 (GRCm39) |
|
probably null |
Het |
Aff1 |
G |
A |
5: 103,988,923 (GRCm39) |
G830D |
probably damaging |
Het |
AI987944 |
T |
C |
7: 41,023,873 (GRCm39) |
T369A |
possibly damaging |
Het |
Arhgap40 |
C |
G |
2: 158,381,190 (GRCm39) |
C349W |
probably damaging |
Het |
Atic |
T |
A |
1: 71,615,286 (GRCm39) |
D438E |
probably benign |
Het |
Barhl2 |
A |
T |
5: 106,601,365 (GRCm39) |
M338K |
probably benign |
Het |
Btd |
T |
C |
14: 31,388,747 (GRCm39) |
V156A |
probably damaging |
Het |
Catspere2 |
A |
G |
1: 177,874,552 (GRCm39) |
K140E |
unknown |
Het |
Ccdc82 |
T |
C |
9: 13,262,397 (GRCm39) |
V319A |
probably damaging |
Het |
Celsr1 |
G |
T |
15: 85,915,263 (GRCm39) |
N903K |
probably damaging |
Het |
Cenpf |
T |
A |
1: 189,389,968 (GRCm39) |
N1288I |
probably damaging |
Het |
Ciao1 |
G |
A |
2: 127,086,857 (GRCm39) |
T252I |
probably benign |
Het |
Cma2 |
T |
C |
14: 56,210,573 (GRCm39) |
C87R |
probably damaging |
Het |
Cops7a |
T |
A |
6: 124,939,401 (GRCm39) |
R83W |
probably damaging |
Het |
Cxcr6 |
A |
T |
9: 123,639,613 (GRCm39) |
M205L |
possibly damaging |
Het |
Dcc |
A |
G |
18: 71,553,409 (GRCm39) |
L749P |
probably benign |
Het |
Dync1i2 |
C |
T |
2: 71,081,323 (GRCm39) |
T484I |
possibly damaging |
Het |
Epas1 |
A |
T |
17: 87,136,455 (GRCm39) |
K742N |
probably damaging |
Het |
Evc2 |
A |
G |
5: 37,506,094 (GRCm39) |
T138A |
probably benign |
Het |
F5 |
T |
C |
1: 164,035,457 (GRCm39) |
I1877T |
probably damaging |
Het |
Fat1 |
T |
G |
8: 45,406,201 (GRCm39) |
V984G |
probably benign |
Het |
Fat4 |
T |
A |
3: 39,034,928 (GRCm39) |
V2860D |
probably damaging |
Het |
Foxn4 |
C |
T |
5: 114,394,955 (GRCm39) |
R324Q |
probably benign |
Het |
Gapdhs |
C |
T |
7: 30,436,427 (GRCm39) |
R120H |
probably damaging |
Het |
Gcnt3 |
T |
C |
9: 69,941,659 (GRCm39) |
D303G |
probably benign |
Het |
Gng11 |
A |
T |
6: 4,008,066 (GRCm39) |
Y43F |
probably benign |
Het |
Hectd4 |
A |
C |
5: 121,455,308 (GRCm39) |
M651L |
probably benign |
Het |
Ifngr2 |
T |
A |
16: 91,357,484 (GRCm39) |
Y200N |
probably benign |
Het |
Iqgap3 |
T |
C |
3: 88,005,708 (GRCm39) |
V512A |
probably benign |
Het |
Kdm2a |
A |
C |
19: 4,378,240 (GRCm39) |
D187E |
probably damaging |
Het |
Klhl8 |
A |
G |
5: 104,019,911 (GRCm39) |
V370A |
probably damaging |
Het |
Kmt2a |
G |
A |
9: 44,747,967 (GRCm39) |
|
probably benign |
Het |
Krt12 |
C |
A |
11: 99,311,650 (GRCm39) |
V184F |
probably benign |
Het |
Lrrc8c |
A |
T |
5: 105,754,623 (GRCm39) |
I133F |
probably benign |
Het |
Lsmem1 |
GTACATACATACATACATACATACATACA |
GTACATACATACATACATACATACATACATACA |
12: 40,235,260 (GRCm39) |
|
probably null |
Het |
Map1a |
C |
G |
2: 121,136,889 (GRCm39) |
S2568R |
possibly damaging |
Het |
Mbnl1 |
C |
A |
3: 60,532,593 (GRCm39) |
Q301K |
probably damaging |
Het |
Med12l |
A |
T |
3: 59,001,038 (GRCm39) |
K724N |
probably damaging |
Het |
Mroh2a |
A |
C |
1: 88,169,340 (GRCm39) |
I672L |
probably benign |
Het |
Mybph |
C |
T |
1: 134,121,374 (GRCm39) |
P45S |
probably benign |
Het |
Myo15a |
T |
A |
11: 60,392,527 (GRCm39) |
S2157T |
probably damaging |
Het |
Or14j2 |
G |
T |
17: 37,886,164 (GRCm39) |
T50K |
probably damaging |
Het |
Or1ab2 |
T |
C |
8: 72,863,623 (GRCm39) |
V71A |
probably benign |
Het |
Or2t35 |
T |
A |
14: 14,407,880 (GRCm38) |
Y217* |
probably null |
Het |
Or5h25 |
T |
C |
16: 58,930,967 (GRCm39) |
E2G |
probably benign |
Het |
Otogl |
A |
G |
10: 107,634,218 (GRCm39) |
I1419T |
possibly damaging |
Het |
Ovol1 |
A |
T |
19: 5,601,667 (GRCm39) |
F118L |
probably damaging |
Het |
Pak5 |
T |
C |
2: 135,958,680 (GRCm39) |
D136G |
probably damaging |
Het |
Pik3r2 |
T |
C |
8: 71,223,250 (GRCm39) |
Y417C |
probably damaging |
Het |
Ppp2r2a |
T |
C |
14: 67,254,052 (GRCm39) |
N372S |
probably benign |
Het |
Prss30 |
G |
T |
17: 24,191,806 (GRCm39) |
N238K |
possibly damaging |
Het |
Prss33 |
C |
A |
17: 24,053,785 (GRCm39) |
|
probably null |
Het |
Ptpn4 |
T |
C |
1: 119,692,788 (GRCm39) |
E187G |
probably damaging |
Het |
Ptprg |
A |
T |
14: 12,207,357 (GRCm38) |
N100I |
probably damaging |
Het |
Rbpms2 |
T |
C |
9: 65,558,324 (GRCm39) |
V130A |
probably benign |
Het |
Rdh7 |
A |
T |
10: 127,724,481 (GRCm39) |
M1K |
probably null |
Het |
Rtp3 |
A |
C |
9: 110,815,751 (GRCm39) |
S205A |
probably benign |
Het |
Ryr3 |
G |
T |
2: 112,539,618 (GRCm39) |
D3207E |
probably damaging |
Het |
Scn9a |
T |
A |
2: 66,313,803 (GRCm39) |
T1972S |
probably benign |
Het |
Scnn1b |
T |
C |
7: 121,501,551 (GRCm39) |
V122A |
probably benign |
Het |
Slc15a4 |
A |
G |
5: 127,686,043 (GRCm39) |
L213S |
probably damaging |
Het |
Slc27a5 |
T |
A |
7: 12,725,173 (GRCm39) |
I425F |
probably damaging |
Het |
Spata31d1b |
A |
G |
13: 59,864,442 (GRCm39) |
D530G |
probably benign |
Het |
Tcf25 |
T |
A |
8: 124,108,289 (GRCm39) |
S115T |
probably benign |
Het |
Tet2 |
A |
G |
3: 133,172,613 (GRCm39) |
L1883P |
possibly damaging |
Het |
Trim21 |
T |
A |
7: 102,211,105 (GRCm39) |
R205* |
probably null |
Het |
Ttc23 |
G |
T |
7: 67,375,069 (GRCm39) |
|
probably null |
Het |
Tut7 |
T |
C |
13: 59,947,717 (GRCm39) |
E466G |
possibly damaging |
Het |
Unc13d |
T |
C |
11: 115,959,499 (GRCm39) |
K658R |
probably null |
Het |
Vmn1r43 |
A |
G |
6: 89,846,572 (GRCm39) |
F305L |
possibly damaging |
Het |
Vmn2r2 |
A |
T |
3: 64,024,551 (GRCm39) |
C677S |
probably benign |
Het |
Wnt5a |
T |
C |
14: 28,240,300 (GRCm39) |
M150T |
probably benign |
Het |
Ythdc1 |
G |
A |
5: 86,975,981 (GRCm39) |
|
probably null |
Het |
Zdbf2 |
A |
T |
1: 63,343,408 (GRCm39) |
R596* |
probably null |
Het |
|
Other mutations in Aoah |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01561:Aoah
|
APN |
13 |
21,089,905 (GRCm39) |
splice site |
probably benign |
|
IGL01561:Aoah
|
APN |
13 |
21,189,264 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL01717:Aoah
|
APN |
13 |
21,184,147 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01997:Aoah
|
APN |
13 |
21,184,108 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02212:Aoah
|
APN |
13 |
21,187,071 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02325:Aoah
|
APN |
13 |
21,101,295 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL03028:Aoah
|
APN |
13 |
21,000,752 (GRCm39) |
missense |
possibly damaging |
0.62 |
IGL03304:Aoah
|
APN |
13 |
21,099,180 (GRCm39) |
splice site |
probably benign |
|
IGL03352:Aoah
|
APN |
13 |
21,184,213 (GRCm39) |
missense |
probably benign |
0.01 |
H8562:Aoah
|
UTSW |
13 |
21,000,694 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4402001:Aoah
|
UTSW |
13 |
20,978,680 (GRCm39) |
missense |
probably benign |
0.00 |
R0255:Aoah
|
UTSW |
13 |
21,163,710 (GRCm39) |
nonsense |
probably null |
|
R0432:Aoah
|
UTSW |
13 |
21,095,368 (GRCm39) |
splice site |
probably benign |
|
R0501:Aoah
|
UTSW |
13 |
21,189,243 (GRCm39) |
missense |
probably benign |
0.16 |
R1036:Aoah
|
UTSW |
13 |
21,024,339 (GRCm39) |
splice site |
probably benign |
|
R1119:Aoah
|
UTSW |
13 |
21,099,108 (GRCm39) |
splice site |
probably benign |
|
R1203:Aoah
|
UTSW |
13 |
21,000,764 (GRCm39) |
missense |
probably damaging |
1.00 |
R1589:Aoah
|
UTSW |
13 |
21,187,118 (GRCm39) |
missense |
probably damaging |
0.99 |
R1907:Aoah
|
UTSW |
13 |
21,094,264 (GRCm39) |
missense |
probably damaging |
1.00 |
R1959:Aoah
|
UTSW |
13 |
20,978,564 (GRCm39) |
start codon destroyed |
probably null |
0.89 |
R2145:Aoah
|
UTSW |
13 |
21,024,266 (GRCm39) |
missense |
probably damaging |
1.00 |
R2237:Aoah
|
UTSW |
13 |
20,978,481 (GRCm39) |
start gained |
probably benign |
|
R3438:Aoah
|
UTSW |
13 |
21,101,242 (GRCm39) |
missense |
probably benign |
0.00 |
R4226:Aoah
|
UTSW |
13 |
21,163,696 (GRCm39) |
missense |
possibly damaging |
0.50 |
R4868:Aoah
|
UTSW |
13 |
21,099,151 (GRCm39) |
nonsense |
probably null |
|
R5026:Aoah
|
UTSW |
13 |
21,099,129 (GRCm39) |
missense |
probably damaging |
1.00 |
R5139:Aoah
|
UTSW |
13 |
21,207,407 (GRCm39) |
missense |
possibly damaging |
0.61 |
R5624:Aoah
|
UTSW |
13 |
21,179,649 (GRCm39) |
missense |
probably damaging |
1.00 |
R5853:Aoah
|
UTSW |
13 |
21,184,072 (GRCm39) |
missense |
probably benign |
0.01 |
R6134:Aoah
|
UTSW |
13 |
21,095,293 (GRCm39) |
missense |
probably damaging |
1.00 |
R6459:Aoah
|
UTSW |
13 |
21,184,112 (GRCm39) |
missense |
probably damaging |
0.99 |
R7077:Aoah
|
UTSW |
13 |
21,094,276 (GRCm39) |
missense |
probably damaging |
1.00 |
R7103:Aoah
|
UTSW |
13 |
21,207,485 (GRCm39) |
missense |
probably damaging |
1.00 |
R8198:Aoah
|
UTSW |
13 |
21,101,290 (GRCm39) |
missense |
probably damaging |
1.00 |
R8340:Aoah
|
UTSW |
13 |
21,184,112 (GRCm39) |
missense |
probably damaging |
0.99 |
R8723:Aoah
|
UTSW |
13 |
21,184,180 (GRCm39) |
missense |
possibly damaging |
0.81 |
R8790:Aoah
|
UTSW |
13 |
21,035,840 (GRCm39) |
missense |
probably benign |
0.16 |
R8811:Aoah
|
UTSW |
13 |
21,184,121 (GRCm39) |
missense |
probably damaging |
1.00 |
R8873:Aoah
|
UTSW |
13 |
21,089,852 (GRCm39) |
missense |
probably benign |
0.00 |
R8973:Aoah
|
UTSW |
13 |
21,024,325 (GRCm39) |
missense |
probably benign |
0.00 |
R9015:Aoah
|
UTSW |
13 |
21,184,197 (GRCm39) |
synonymous |
silent |
|
R9287:Aoah
|
UTSW |
13 |
21,186,879 (GRCm39) |
missense |
probably damaging |
0.96 |
R9759:Aoah
|
UTSW |
13 |
21,000,738 (GRCm39) |
missense |
probably damaging |
1.00 |
|