Other mutations in this stock |
Total: 79 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4933430I17Rik |
T |
C |
4: 62,450,515 (GRCm39) |
W30R |
probably damaging |
Het |
Abca3 |
A |
G |
17: 24,627,199 (GRCm39) |
D1555G |
probably benign |
Het |
Anapc1 |
T |
C |
2: 128,483,373 (GRCm39) |
T1241A |
probably damaging |
Het |
Ano5 |
G |
A |
7: 51,243,519 (GRCm39) |
V881I |
probably benign |
Het |
Appl1 |
G |
A |
14: 26,662,212 (GRCm39) |
S490L |
probably benign |
Het |
Asxl3 |
A |
G |
18: 22,567,664 (GRCm39) |
T81A |
probably benign |
Het |
Bclaf1 |
T |
C |
10: 20,209,184 (GRCm39) |
S754P |
possibly damaging |
Het |
Bicra |
G |
T |
7: 15,723,113 (GRCm39) |
Q135K |
probably benign |
Het |
Cad |
T |
C |
5: 31,233,605 (GRCm39) |
V1951A |
possibly damaging |
Het |
Cadm3 |
T |
A |
1: 173,168,683 (GRCm39) |
Y295F |
probably damaging |
Het |
Ccnt1 |
A |
G |
15: 98,462,995 (GRCm39) |
I59T |
probably damaging |
Het |
Ccr6 |
C |
T |
17: 8,475,398 (GRCm39) |
T201M |
probably benign |
Het |
Cd5 |
A |
G |
19: 10,702,556 (GRCm39) |
F209S |
possibly damaging |
Het |
Cep126 |
A |
C |
9: 8,087,362 (GRCm39) |
D1017E |
probably damaging |
Het |
Cfap298 |
T |
C |
16: 90,727,945 (GRCm39) |
K82E |
probably benign |
Het |
Cntnap4 |
A |
T |
8: 113,484,228 (GRCm39) |
D427V |
probably damaging |
Het |
Col4a4 |
T |
A |
1: 82,433,455 (GRCm39) |
N1496I |
unknown |
Het |
Crybg3 |
A |
G |
16: 59,375,291 (GRCm39) |
Y274H |
probably damaging |
Het |
Cubn |
C |
A |
2: 13,388,770 (GRCm39) |
S1479I |
probably damaging |
Het |
Diras2 |
A |
T |
13: 52,662,143 (GRCm39) |
C55S |
probably damaging |
Het |
Dleu7 |
G |
A |
14: 62,530,279 (GRCm39) |
R41C |
probably benign |
Het |
Dync2i1 |
T |
C |
12: 116,171,321 (GRCm39) |
T972A |
probably benign |
Het |
Efcab3 |
A |
G |
11: 104,672,072 (GRCm39) |
T1464A |
probably benign |
Het |
Exo5 |
A |
G |
4: 120,779,193 (GRCm39) |
I224T |
probably damaging |
Het |
Fcho1 |
T |
C |
8: 72,162,277 (GRCm39) |
I774V |
possibly damaging |
Het |
Gclm |
T |
G |
3: 122,059,972 (GRCm39) |
S251A |
possibly damaging |
Het |
Gm13889 |
T |
C |
2: 93,787,327 (GRCm39) |
Q49R |
unknown |
Het |
Gm35315 |
T |
A |
5: 110,228,392 (GRCm39) |
H18L |
probably benign |
Het |
Gm9949 |
G |
A |
18: 62,317,043 (GRCm39) |
G65R |
unknown |
Het |
Gpr153 |
C |
T |
4: 152,363,558 (GRCm39) |
|
probably benign |
Het |
Gria4 |
C |
A |
9: 4,424,347 (GRCm39) |
K839N |
probably damaging |
Het |
Gria4 |
T |
G |
9: 4,424,351 (GRCm39) |
Y838S |
probably damaging |
Het |
Hrh3 |
A |
G |
2: 179,743,149 (GRCm39) |
W160R |
probably damaging |
Het |
Htr4 |
G |
A |
18: 62,570,763 (GRCm39) |
A273T |
probably damaging |
Het |
Lig3 |
G |
T |
11: 82,685,376 (GRCm39) |
C599F |
probably damaging |
Het |
Lrp1b |
A |
T |
2: 41,172,207 (GRCm39) |
V1594E |
|
Het |
Map3k10 |
A |
T |
7: 27,367,780 (GRCm39) |
V286D |
probably damaging |
Het |
Map4k4 |
T |
A |
1: 40,015,910 (GRCm39) |
V117E |
unknown |
Het |
Mdga1 |
C |
T |
17: 30,061,348 (GRCm39) |
V548M |
possibly damaging |
Het |
Mms22l |
A |
T |
4: 24,507,363 (GRCm39) |
L248F |
possibly damaging |
Het |
Ncaph |
T |
C |
2: 126,963,096 (GRCm39) |
D379G |
possibly damaging |
Het |
Neb |
A |
G |
2: 52,037,246 (GRCm39) |
V7064A |
probably benign |
Het |
Neb |
G |
A |
2: 52,102,563 (GRCm39) |
T4570M |
probably benign |
Het |
Npy5r |
G |
T |
8: 67,134,274 (GRCm39) |
T173K |
probably damaging |
Het |
Or5b94 |
A |
G |
19: 12,652,246 (GRCm39) |
M226V |
probably benign |
Het |
Or5b97 |
A |
T |
19: 12,878,828 (GRCm39) |
F105L |
possibly damaging |
Het |
Or5g25 |
A |
T |
2: 85,478,330 (GRCm39) |
C112S |
possibly damaging |
Het |
Or8u10 |
A |
T |
2: 85,915,518 (GRCm39) |
I201N |
probably damaging |
Het |
Oxsm |
A |
G |
14: 16,242,631 (GRCm38) |
I46T |
possibly damaging |
Het |
Pcdha1 |
A |
T |
18: 37,064,076 (GRCm39) |
I247F |
probably benign |
Het |
Pcdhgb6 |
A |
T |
18: 37,875,975 (GRCm39) |
I228L |
probably benign |
Het |
Peg10 |
T |
TCCA |
6: 4,756,451 (GRCm39) |
|
probably benign |
Het |
Ppp1r9a |
A |
G |
6: 5,115,474 (GRCm39) |
S866G |
probably benign |
Het |
Ppp6r3 |
T |
A |
19: 3,546,587 (GRCm39) |
S304C |
probably damaging |
Het |
Pramel11 |
A |
T |
4: 143,623,762 (GRCm39) |
N137K |
probably benign |
Het |
Ptprd |
A |
T |
4: 75,959,629 (GRCm39) |
F279I |
probably benign |
Het |
Repin1 |
G |
T |
6: 48,574,279 (GRCm39) |
E403* |
probably null |
Het |
Rest |
G |
A |
5: 77,429,389 (GRCm39) |
G603R |
probably benign |
Het |
Rgs17 |
A |
T |
10: 5,868,194 (GRCm39) |
L9M |
probably benign |
Het |
Rtp1 |
A |
G |
16: 23,250,133 (GRCm39) |
Y166C |
probably damaging |
Het |
Sec24b |
C |
A |
3: 129,798,653 (GRCm39) |
R572I |
probably damaging |
Het |
Setd1a |
G |
T |
7: 127,385,774 (GRCm39) |
R827L |
possibly damaging |
Het |
Sh3tc1 |
T |
C |
5: 35,859,235 (GRCm39) |
Y1091C |
probably damaging |
Het |
Sorbs1 |
G |
C |
19: 40,365,244 (GRCm39) |
R180G |
probably benign |
Het |
Stat4 |
T |
A |
1: 52,111,096 (GRCm39) |
M181K |
probably benign |
Het |
Stk16 |
A |
G |
1: 75,188,682 (GRCm39) |
E67G |
probably benign |
Het |
Supv3l1 |
A |
G |
10: 62,268,234 (GRCm39) |
V537A |
possibly damaging |
Het |
Tmc8 |
A |
G |
11: 117,674,361 (GRCm39) |
E101G |
possibly damaging |
Het |
Tmem106a |
A |
T |
11: 101,473,120 (GRCm39) |
|
probably benign |
Het |
Tpr |
T |
A |
1: 150,293,772 (GRCm39) |
I922N |
probably damaging |
Het |
Uaca |
G |
T |
9: 60,778,347 (GRCm39) |
L911F |
probably damaging |
Het |
Ubn1 |
A |
T |
16: 4,881,567 (GRCm39) |
I200L |
possibly damaging |
Het |
Ush2a |
A |
G |
1: 188,643,574 (GRCm39) |
D4312G |
probably damaging |
Het |
Virma |
A |
T |
4: 11,528,678 (GRCm39) |
Y1255F |
probably benign |
Het |
Vmn1r170 |
C |
T |
7: 23,306,080 (GRCm39) |
Q161* |
probably null |
Het |
Vmn1r175 |
G |
T |
7: 23,508,234 (GRCm39) |
A131D |
probably benign |
Het |
Vmn1r52 |
T |
A |
6: 90,155,742 (GRCm39) |
N15K |
probably benign |
Het |
Wdr46 |
T |
A |
17: 34,167,826 (GRCm39) |
I513N |
probably damaging |
Het |
Zfp788 |
A |
G |
7: 41,297,840 (GRCm39) |
N159D |
probably benign |
Het |
|
Other mutations in Or52a33 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01445:Or52a33
|
APN |
7 |
103,289,039 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02972:Or52a33
|
APN |
7 |
103,289,101 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4434001:Or52a33
|
UTSW |
7 |
103,289,054 (GRCm39) |
missense |
probably damaging |
1.00 |
R1487:Or52a33
|
UTSW |
7 |
103,288,801 (GRCm39) |
missense |
probably damaging |
1.00 |
R1989:Or52a33
|
UTSW |
7 |
103,288,702 (GRCm39) |
missense |
probably damaging |
1.00 |
R3880:Or52a33
|
UTSW |
7 |
103,288,831 (GRCm39) |
missense |
probably benign |
0.33 |
R4595:Or52a33
|
UTSW |
7 |
103,289,308 (GRCm39) |
missense |
probably damaging |
1.00 |
R4989:Or52a33
|
UTSW |
7 |
103,289,308 (GRCm39) |
missense |
probably damaging |
1.00 |
R5715:Or52a33
|
UTSW |
7 |
103,289,009 (GRCm39) |
missense |
probably damaging |
1.00 |
R5840:Or52a33
|
UTSW |
7 |
103,288,463 (GRCm39) |
missense |
probably benign |
0.05 |
R6046:Or52a33
|
UTSW |
7 |
103,288,886 (GRCm39) |
missense |
probably benign |
0.01 |
R6207:Or52a33
|
UTSW |
7 |
103,289,209 (GRCm39) |
missense |
probably benign |
0.29 |
R6294:Or52a33
|
UTSW |
7 |
103,288,798 (GRCm39) |
missense |
probably damaging |
1.00 |
R6392:Or52a33
|
UTSW |
7 |
103,288,889 (GRCm39) |
missense |
probably benign |
|
R6522:Or52a33
|
UTSW |
7 |
103,288,504 (GRCm39) |
missense |
probably damaging |
1.00 |
R6996:Or52a33
|
UTSW |
7 |
103,289,065 (GRCm39) |
missense |
probably benign |
0.10 |
R7069:Or52a33
|
UTSW |
7 |
103,289,167 (GRCm39) |
missense |
probably damaging |
0.99 |
R7251:Or52a33
|
UTSW |
7 |
103,288,909 (GRCm39) |
missense |
probably damaging |
1.00 |
R7625:Or52a33
|
UTSW |
7 |
103,289,165 (GRCm39) |
missense |
probably damaging |
1.00 |
R8309:Or52a33
|
UTSW |
7 |
103,288,658 (GRCm39) |
missense |
probably damaging |
1.00 |
R8750:Or52a33
|
UTSW |
7 |
103,289,059 (GRCm39) |
missense |
probably damaging |
0.97 |
R8949:Or52a33
|
UTSW |
7 |
103,288,702 (GRCm39) |
missense |
probably damaging |
1.00 |
X0018:Or52a33
|
UTSW |
7 |
103,288,805 (GRCm39) |
missense |
probably damaging |
1.00 |
|