Other mutations in this stock |
Total: 81 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110002E22Rik |
C |
A |
3: 137,770,909 (GRCm39) |
Q33K |
possibly damaging |
Het |
Acap2 |
A |
G |
16: 30,925,906 (GRCm39) |
L550P |
probably damaging |
Het |
Acsm3 |
A |
T |
7: 119,373,845 (GRCm39) |
S244C |
probably benign |
Het |
Adam28 |
T |
A |
14: 68,846,593 (GRCm39) |
D740V |
probably benign |
Het |
Adcy4 |
C |
A |
14: 56,016,426 (GRCm39) |
V342L |
probably damaging |
Het |
Adcyap1r1 |
A |
G |
6: 55,458,107 (GRCm39) |
T303A |
probably benign |
Het |
Agr2 |
T |
C |
12: 36,046,091 (GRCm39) |
V74A |
probably benign |
Het |
Akp3 |
A |
T |
1: 87,054,786 (GRCm39) |
T374S |
possibly damaging |
Het |
Ankrd36 |
A |
T |
11: 5,610,696 (GRCm39) |
I1181L |
probably benign |
Het |
Arhgap11a |
A |
T |
2: 113,664,411 (GRCm39) |
V624E |
probably benign |
Het |
Arhgap30 |
A |
T |
1: 171,228,258 (GRCm39) |
D112V |
probably damaging |
Het |
Atp8b4 |
A |
G |
2: 126,184,883 (GRCm39) |
F927L |
probably benign |
Het |
Bend4 |
C |
A |
5: 67,584,475 (GRCm39) |
G150C |
unknown |
Het |
Cd300lg |
T |
A |
11: 101,944,998 (GRCm39) |
S403T |
probably damaging |
Het |
Cep57l1 |
T |
A |
10: 41,607,086 (GRCm39) |
Q159L |
probably damaging |
Het |
Cipc |
C |
T |
12: 86,999,634 (GRCm39) |
T57M |
probably damaging |
Het |
Def8 |
T |
C |
8: 124,186,391 (GRCm39) |
C377R |
probably damaging |
Het |
Dock1 |
A |
G |
7: 134,720,746 (GRCm39) |
D1285G |
probably damaging |
Het |
Efcab10 |
A |
G |
12: 33,448,398 (GRCm39) |
D77G |
probably damaging |
Het |
Eml4 |
C |
T |
17: 83,764,479 (GRCm39) |
T663M |
probably damaging |
Het |
Ercc8 |
A |
G |
13: 108,320,389 (GRCm39) |
E325G |
possibly damaging |
Het |
Ermap |
C |
A |
4: 119,035,240 (GRCm39) |
A583S |
probably damaging |
Het |
F13a1 |
C |
T |
13: 37,102,506 (GRCm39) |
G406S |
probably null |
Het |
Faap20 |
T |
A |
4: 155,335,426 (GRCm39) |
C141S |
probably benign |
Het |
Fam193a |
A |
G |
5: 34,616,536 (GRCm39) |
T904A |
possibly damaging |
Het |
Garin2 |
T |
C |
12: 78,757,097 (GRCm39) |
F18S |
probably benign |
Het |
Gas8 |
A |
G |
8: 124,260,134 (GRCm39) |
D455G |
probably benign |
Het |
Gm21863 |
T |
C |
12: 20,004,521 (GRCm39) |
S6P |
probably damaging |
Het |
Gm4841 |
A |
T |
18: 60,403,988 (GRCm39) |
I35N |
probably damaging |
Het |
Grk4 |
T |
A |
5: 34,877,084 (GRCm39) |
C260S |
probably damaging |
Het |
Huwe1 |
G |
A |
X: 150,716,084 (GRCm39) |
R4331Q |
unknown |
Het |
Ighv5-6 |
A |
G |
12: 113,589,247 (GRCm39) |
Y78H |
probably benign |
Het |
Itpr3 |
G |
A |
17: 27,337,651 (GRCm39) |
|
probably benign |
Het |
Kl |
T |
A |
5: 150,876,491 (GRCm39) |
S104T |
probably benign |
Het |
Lyve1 |
C |
A |
7: 110,453,182 (GRCm39) |
C138F |
probably damaging |
Het |
Med27 |
G |
A |
2: 29,399,446 (GRCm39) |
W92* |
probably null |
Het |
Mical3 |
A |
T |
6: 120,986,848 (GRCm39) |
|
probably benign |
Het |
Mrgpra4 |
C |
A |
7: 47,631,208 (GRCm39) |
R131L |
possibly damaging |
Het |
Myf5 |
T |
C |
10: 107,321,308 (GRCm39) |
N162S |
probably benign |
Het |
Myh15 |
G |
A |
16: 49,007,433 (GRCm39) |
E1835K |
probably damaging |
Het |
Myo9a |
T |
A |
9: 59,716,757 (GRCm39) |
Y486N |
probably damaging |
Het |
Ncapg |
T |
A |
5: 45,853,115 (GRCm39) |
N860K |
probably benign |
Het |
Nr4a3 |
T |
C |
4: 48,052,194 (GRCm39) |
F316S |
possibly damaging |
Het |
Nsd3 |
T |
A |
8: 26,172,576 (GRCm39) |
S778R |
probably benign |
Het |
Or2r2 |
A |
G |
6: 42,463,795 (GRCm39) |
F111L |
probably damaging |
Het |
Or4c119 |
A |
T |
2: 88,986,988 (GRCm39) |
V177E |
probably benign |
Het |
Or4c31 |
A |
G |
2: 88,292,196 (GRCm39) |
I190V |
probably damaging |
Het |
Or5p6 |
A |
G |
7: 107,631,286 (GRCm39) |
F88S |
probably damaging |
Het |
Or7e173 |
T |
C |
9: 19,938,344 (GRCm39) |
N297D |
|
Het |
Or8w1 |
A |
T |
2: 87,465,369 (GRCm39) |
C241S |
probably damaging |
Het |
Or9m2 |
A |
G |
2: 87,820,568 (GRCm39) |
T38A |
probably damaging |
Het |
Pdlim4 |
C |
T |
11: 53,946,280 (GRCm39) |
G231S |
probably benign |
Het |
Pknox2 |
C |
T |
9: 36,821,044 (GRCm39) |
V273I |
possibly damaging |
Het |
Pm20d1 |
A |
G |
1: 131,739,822 (GRCm39) |
H390R |
probably benign |
Het |
Prkg2 |
A |
T |
5: 99,114,386 (GRCm39) |
D587E |
probably benign |
Het |
Prps1l1 |
T |
A |
12: 35,035,546 (GRCm39) |
D220E |
possibly damaging |
Het |
Prss3l |
A |
G |
6: 41,422,990 (GRCm39) |
F4L |
probably benign |
Het |
Ptchd3 |
T |
C |
11: 121,721,682 (GRCm39) |
V185A |
possibly damaging |
Het |
Rag2 |
A |
T |
2: 101,460,494 (GRCm39) |
N268I |
possibly damaging |
Het |
Rarres2 |
A |
G |
6: 48,549,020 (GRCm39) |
|
probably null |
Het |
Rrp12 |
T |
C |
19: 41,860,223 (GRCm39) |
H1000R |
probably benign |
Het |
S100a2 |
A |
T |
3: 90,498,811 (GRCm39) |
Y104F |
unknown |
Het |
Sell |
A |
G |
1: 163,893,042 (GRCm39) |
Y86C |
probably damaging |
Het |
Serpinb6d |
A |
T |
13: 33,851,656 (GRCm39) |
T138S |
possibly damaging |
Het |
Slamf7 |
T |
A |
1: 171,466,312 (GRCm39) |
I228F |
probably benign |
Het |
Slc11a1 |
G |
A |
1: 74,416,325 (GRCm39) |
V92M |
probably damaging |
Het |
Spi1 |
A |
G |
2: 90,912,862 (GRCm39) |
N5S |
unknown |
Het |
Stard9 |
G |
T |
2: 120,536,283 (GRCm39) |
D4151Y |
probably damaging |
Het |
Stmnd1 |
A |
G |
13: 46,452,983 (GRCm39) |
T220A |
probably benign |
Het |
Tacc2 |
G |
T |
7: 130,225,266 (GRCm39) |
W650C |
probably damaging |
Het |
Tmc5 |
A |
G |
7: 118,241,594 (GRCm39) |
N429S |
possibly damaging |
Het |
Tmem201 |
A |
C |
4: 149,812,627 (GRCm39) |
L230V |
probably benign |
Het |
Tmem222 |
T |
C |
4: 132,997,119 (GRCm39) |
E94G |
possibly damaging |
Het |
Trappc4 |
A |
G |
9: 44,315,655 (GRCm39) |
F186S |
probably damaging |
Het |
Trim17 |
A |
G |
11: 58,862,273 (GRCm39) |
N435S |
probably benign |
Het |
Trim68 |
A |
T |
7: 102,329,447 (GRCm39) |
L227Q |
probably damaging |
Het |
Tuba3b |
T |
G |
6: 145,563,996 (GRCm39) |
V14G |
possibly damaging |
Het |
Ubr2 |
G |
T |
17: 47,245,041 (GRCm39) |
H1662N |
probably damaging |
Het |
Vps13c |
T |
A |
9: 67,861,863 (GRCm39) |
V2915E |
probably damaging |
Het |
Vsig10 |
C |
T |
5: 117,476,323 (GRCm39) |
T259I |
probably benign |
Het |
Zfp267 |
A |
G |
3: 36,219,066 (GRCm39) |
Y363C |
possibly damaging |
Het |
|
Other mutations in Or8b37 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00870:Or8b37
|
APN |
9 |
37,959,036 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02612:Or8b37
|
APN |
9 |
37,958,662 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02802:Or8b37
|
UTSW |
9 |
37,959,345 (GRCm39) |
missense |
probably damaging |
0.99 |
R0015:Or8b37
|
UTSW |
9 |
37,958,963 (GRCm39) |
nonsense |
probably null |
|
R0142:Or8b37
|
UTSW |
9 |
37,959,406 (GRCm39) |
missense |
probably benign |
0.37 |
R0559:Or8b37
|
UTSW |
9 |
37,959,123 (GRCm39) |
missense |
probably benign |
0.16 |
R0561:Or8b37
|
UTSW |
9 |
37,959,123 (GRCm39) |
missense |
probably benign |
0.16 |
R0715:Or8b37
|
UTSW |
9 |
37,959,123 (GRCm39) |
missense |
probably benign |
0.16 |
R0723:Or8b37
|
UTSW |
9 |
37,959,123 (GRCm39) |
missense |
probably benign |
0.16 |
R0729:Or8b37
|
UTSW |
9 |
37,959,123 (GRCm39) |
missense |
probably benign |
0.16 |
R1350:Or8b37
|
UTSW |
9 |
37,959,111 (GRCm39) |
missense |
probably benign |
0.02 |
R1869:Or8b37
|
UTSW |
9 |
37,959,498 (GRCm39) |
splice site |
probably null |
|
R3917:Or8b37
|
UTSW |
9 |
37,958,841 (GRCm39) |
missense |
probably damaging |
1.00 |
R4131:Or8b37
|
UTSW |
9 |
37,959,170 (GRCm39) |
nonsense |
probably null |
|
R4764:Or8b37
|
UTSW |
9 |
37,959,436 (GRCm39) |
missense |
probably benign |
|
R5857:Or8b37
|
UTSW |
9 |
37,959,049 (GRCm39) |
missense |
probably benign |
0.18 |
R5976:Or8b37
|
UTSW |
9 |
37,958,997 (GRCm39) |
missense |
possibly damaging |
0.80 |
R6329:Or8b37
|
UTSW |
9 |
37,959,121 (GRCm39) |
missense |
probably benign |
0.02 |
R7344:Or8b37
|
UTSW |
9 |
37,959,253 (GRCm39) |
missense |
probably benign |
|
R8289:Or8b37
|
UTSW |
9 |
37,959,000 (GRCm39) |
missense |
probably benign |
0.02 |
R8485:Or8b37
|
UTSW |
9 |
37,959,253 (GRCm39) |
missense |
probably benign |
0.00 |
R8973:Or8b37
|
UTSW |
9 |
37,958,839 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9378:Or8b37
|
UTSW |
9 |
37,958,775 (GRCm39) |
missense |
possibly damaging |
0.67 |
R9395:Or8b37
|
UTSW |
9 |
37,959,136 (GRCm39) |
missense |
probably damaging |
0.99 |
R9655:Or8b37
|
UTSW |
9 |
37,959,387 (GRCm39) |
missense |
probably benign |
0.00 |
R9731:Or8b37
|
UTSW |
9 |
37,958,892 (GRCm39) |
missense |
probably damaging |
1.00 |
RF009:Or8b37
|
UTSW |
9 |
37,959,043 (GRCm39) |
missense |
probably damaging |
1.00 |
X0052:Or8b37
|
UTSW |
9 |
37,958,995 (GRCm39) |
missense |
possibly damaging |
0.53 |
Z1177:Or8b37
|
UTSW |
9 |
37,959,111 (GRCm39) |
missense |
possibly damaging |
0.95 |
|