Other mutations in this stock |
Total: 59 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2210408I21Rik |
A |
T |
13: 77,429,234 (GRCm39) |
I774F |
probably benign |
Het |
Alpi |
A |
G |
1: 87,026,384 (GRCm39) |
S536P |
unknown |
Het |
Ankar |
A |
G |
1: 72,705,643 (GRCm39) |
V789A |
possibly damaging |
Het |
Atp5f1b |
C |
A |
10: 127,919,277 (GRCm39) |
Q28K |
unknown |
Het |
Brpf1 |
T |
C |
6: 113,296,050 (GRCm39) |
V781A |
probably benign |
Het |
Cd177 |
G |
A |
7: 24,451,774 (GRCm39) |
S414L |
not run |
Het |
Cimip3 |
T |
A |
17: 47,747,661 (GRCm39) |
E28V |
probably damaging |
Het |
Clca3b |
T |
A |
3: 144,550,370 (GRCm39) |
T192S |
probably benign |
Het |
Coro2a |
A |
T |
4: 46,551,349 (GRCm39) |
S119T |
probably damaging |
Het |
Cpped1 |
T |
C |
16: 11,646,260 (GRCm39) |
N164S |
probably damaging |
Het |
Crybg2 |
T |
A |
4: 133,818,415 (GRCm39) |
N1390K |
probably damaging |
Het |
Epn2 |
C |
T |
11: 61,437,492 (GRCm39) |
A27T |
probably damaging |
Het |
Esp34 |
T |
C |
17: 38,870,490 (GRCm39) |
F128S |
possibly damaging |
Het |
Evpl |
T |
A |
11: 116,121,298 (GRCm39) |
N410Y |
probably null |
Het |
Flnb |
A |
G |
14: 7,892,155 (GRCm38) |
Y608C |
probably damaging |
Het |
Fpr3 |
T |
C |
17: 18,191,715 (GRCm39) |
S329P |
probably benign |
Het |
Frem2 |
T |
A |
3: 53,560,331 (GRCm39) |
N1392I |
probably damaging |
Het |
Garin2 |
T |
A |
12: 78,761,817 (GRCm39) |
D160E |
probably benign |
Het |
Gpi1 |
G |
T |
7: 33,917,726 (GRCm39) |
N249K |
probably damaging |
Het |
Gpr87 |
T |
C |
3: 59,087,466 (GRCm39) |
N13S |
probably benign |
Het |
Gys2 |
T |
C |
6: 142,400,243 (GRCm39) |
T323A |
probably damaging |
Het |
Iqgap3 |
T |
C |
3: 88,016,770 (GRCm39) |
I1084T |
probably damaging |
Het |
Lrfn4 |
C |
G |
19: 4,663,565 (GRCm39) |
G323A |
probably benign |
Het |
Lrrc4c |
A |
T |
2: 97,460,594 (GRCm39) |
S407C |
possibly damaging |
Het |
Map3k20 |
A |
T |
2: 72,268,613 (GRCm39) |
Q540L |
probably benign |
Het |
Myom1 |
T |
C |
17: 71,407,057 (GRCm39) |
V1158A |
probably benign |
Het |
Ncor2 |
T |
C |
5: 125,144,983 (GRCm39) |
D378G |
unknown |
Het |
Nhsl1 |
T |
A |
10: 18,284,186 (GRCm39) |
D42E |
probably damaging |
Het |
Nr0b2 |
C |
A |
4: 133,283,339 (GRCm39) |
A192E |
probably benign |
Het |
Nt5c1b |
A |
G |
12: 10,425,000 (GRCm39) |
D182G |
possibly damaging |
Het |
Or12d14-ps1 |
T |
C |
17: 37,673,265 (GRCm39) |
S86P |
probably damaging |
Het |
Or4c115 |
A |
T |
2: 88,928,059 (GRCm39) |
C71S |
probably benign |
Het |
Or5k15 |
T |
C |
16: 58,710,251 (GRCm39) |
T111A |
probably benign |
Het |
Or8b12 |
A |
T |
9: 37,658,089 (GRCm39) |
I220F |
probably damaging |
Het |
Pepd |
A |
G |
7: 34,721,126 (GRCm39) |
N250S |
probably benign |
Het |
Plscr4 |
C |
T |
9: 92,372,843 (GRCm39) |
R322* |
probably null |
Het |
Pmp22 |
C |
T |
11: 63,049,233 (GRCm39) |
R159C |
probably damaging |
Het |
Pou3f1 |
C |
T |
4: 124,552,764 (GRCm39) |
A422V |
unknown |
Het |
Rab11fip3 |
A |
G |
17: 26,286,956 (GRCm39) |
L399P |
probably damaging |
Het |
Rragc |
A |
G |
4: 123,829,340 (GRCm39) |
D352G |
probably damaging |
Het |
Ryr2 |
A |
G |
13: 11,671,980 (GRCm39) |
V3420A |
probably benign |
Het |
Sez6 |
T |
A |
11: 77,864,082 (GRCm39) |
Y521* |
probably null |
Het |
Smc4 |
T |
C |
3: 68,914,645 (GRCm39) |
V86A |
probably damaging |
Het |
Stap2 |
T |
A |
17: 56,304,790 (GRCm39) |
M331L |
probably benign |
Het |
Syt8 |
G |
A |
7: 141,992,259 (GRCm39) |
R89H |
probably benign |
Het |
Tcof1 |
G |
C |
18: 60,962,123 (GRCm39) |
A702G |
possibly damaging |
Het |
Trim21 |
G |
T |
7: 102,209,183 (GRCm39) |
T280K |
probably benign |
Het |
Trim36 |
C |
A |
18: 46,305,556 (GRCm39) |
V476F |
probably benign |
Het |
Troap |
G |
T |
15: 98,973,511 (GRCm39) |
R56L |
probably benign |
Het |
Ttn |
A |
T |
2: 76,667,130 (GRCm39) |
I11492K |
unknown |
Het |
Tuft1 |
T |
C |
3: 94,521,440 (GRCm39) |
T390A |
probably damaging |
Het |
Ucp1 |
T |
C |
8: 84,020,640 (GRCm39) |
I150T |
probably benign |
Het |
Usp17lb |
A |
T |
7: 104,490,481 (GRCm39) |
C149S |
possibly damaging |
Het |
Vmn1r159 |
A |
T |
7: 22,542,665 (GRCm39) |
N122K |
possibly damaging |
Het |
Vmn1r237 |
T |
C |
17: 21,534,456 (GRCm39) |
C60R |
probably damaging |
Het |
Wdr12 |
A |
T |
1: 60,128,494 (GRCm39) |
Y85* |
probably null |
Het |
Wdr3 |
T |
C |
3: 100,062,252 (GRCm39) |
D221G |
probably benign |
Het |
Wdr97 |
G |
A |
15: 76,244,832 (GRCm39) |
E1125K |
|
Het |
Zan |
T |
C |
5: 137,403,624 (GRCm39) |
E3974G |
unknown |
Het |
|
Other mutations in Or5b119 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01140:Or5b119
|
APN |
19 |
13,457,151 (GRCm39) |
missense |
possibly damaging |
0.81 |
IGL01604:Or5b119
|
APN |
19 |
13,456,612 (GRCm39) |
unclassified |
probably benign |
|
IGL01656:Or5b119
|
APN |
19 |
13,457,454 (GRCm39) |
missense |
probably benign |
0.08 |
IGL01802:Or5b119
|
APN |
19 |
13,456,729 (GRCm39) |
missense |
probably benign |
0.05 |
IGL01839:Or5b119
|
APN |
19 |
13,456,804 (GRCm39) |
missense |
probably benign |
|
IGL02255:Or5b119
|
APN |
19 |
13,457,349 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02706:Or5b119
|
APN |
19 |
13,457,462 (GRCm39) |
nonsense |
probably null |
|
IGL02723:Or5b119
|
APN |
19 |
13,456,699 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03143:Or5b119
|
APN |
19 |
13,456,835 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03174:Or5b119
|
APN |
19 |
13,457,433 (GRCm39) |
missense |
probably benign |
0.10 |
BB007:Or5b119
|
UTSW |
19 |
13,457,019 (GRCm39) |
missense |
probably damaging |
0.99 |
BB017:Or5b119
|
UTSW |
19 |
13,457,019 (GRCm39) |
missense |
probably damaging |
0.99 |
R0442:Or5b119
|
UTSW |
19 |
13,457,412 (GRCm39) |
missense |
probably damaging |
1.00 |
R0490:Or5b119
|
UTSW |
19 |
13,456,857 (GRCm39) |
missense |
probably damaging |
0.98 |
R0491:Or5b119
|
UTSW |
19 |
13,456,857 (GRCm39) |
missense |
probably damaging |
0.98 |
R1757:Or5b119
|
UTSW |
19 |
13,456,971 (GRCm39) |
missense |
possibly damaging |
0.67 |
R1843:Or5b119
|
UTSW |
19 |
13,457,295 (GRCm39) |
missense |
probably benign |
0.00 |
R1972:Or5b119
|
UTSW |
19 |
13,457,058 (GRCm39) |
missense |
probably benign |
0.00 |
R2137:Or5b119
|
UTSW |
19 |
13,457,173 (GRCm39) |
missense |
probably damaging |
1.00 |
R3150:Or5b119
|
UTSW |
19 |
13,456,824 (GRCm39) |
missense |
probably damaging |
1.00 |
R3858:Or5b119
|
UTSW |
19 |
13,457,494 (GRCm39) |
missense |
possibly damaging |
0.86 |
R3859:Or5b119
|
UTSW |
19 |
13,457,494 (GRCm39) |
missense |
possibly damaging |
0.86 |
R3953:Or5b119
|
UTSW |
19 |
13,456,806 (GRCm39) |
missense |
probably benign |
0.43 |
R4611:Or5b119
|
UTSW |
19 |
13,457,376 (GRCm39) |
missense |
probably damaging |
0.96 |
R4934:Or5b119
|
UTSW |
19 |
13,456,956 (GRCm39) |
missense |
possibly damaging |
0.65 |
R5580:Or5b119
|
UTSW |
19 |
13,456,791 (GRCm39) |
missense |
probably damaging |
1.00 |
R6278:Or5b119
|
UTSW |
19 |
13,457,119 (GRCm39) |
missense |
probably benign |
|
R6444:Or5b119
|
UTSW |
19 |
13,456,794 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6796:Or5b119
|
UTSW |
19 |
13,457,278 (GRCm39) |
missense |
probably damaging |
1.00 |
R6812:Or5b119
|
UTSW |
19 |
13,456,975 (GRCm39) |
missense |
probably benign |
0.03 |
R7608:Or5b119
|
UTSW |
19 |
13,456,956 (GRCm39) |
missense |
possibly damaging |
0.65 |
R7632:Or5b119
|
UTSW |
19 |
13,456,795 (GRCm39) |
missense |
possibly damaging |
0.79 |
R7930:Or5b119
|
UTSW |
19 |
13,457,019 (GRCm39) |
missense |
probably damaging |
0.99 |
R8416:Or5b119
|
UTSW |
19 |
13,456,764 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8551:Or5b119
|
UTSW |
19 |
13,457,109 (GRCm39) |
missense |
possibly damaging |
0.88 |
R9058:Or5b119
|
UTSW |
19 |
13,456,956 (GRCm39) |
missense |
possibly damaging |
0.65 |
R9719:Or5b119
|
UTSW |
19 |
13,457,368 (GRCm39) |
missense |
probably damaging |
1.00 |
R9756:Or5b119
|
UTSW |
19 |
13,456,986 (GRCm39) |
missense |
probably benign |
0.01 |
|