Other mutations in this stock |
Total: 63 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110002E22Rik |
C |
T |
3: 137,775,874 (GRCm39) |
P1688S |
probably benign |
Het |
4933412E24Rik |
T |
C |
15: 59,887,919 (GRCm39) |
T174A |
probably benign |
Het |
Actl10 |
T |
A |
2: 154,395,068 (GRCm39) |
L340Q |
probably damaging |
Het |
Adra1d |
T |
C |
2: 131,403,397 (GRCm39) |
E231G |
probably damaging |
Het |
Agt |
T |
A |
8: 125,291,028 (GRCm39) |
D93V |
probably benign |
Het |
Als2cl |
G |
T |
9: 110,718,282 (GRCm39) |
R341L |
possibly damaging |
Het |
Ankrd63 |
G |
T |
2: 118,533,549 (GRCm39) |
A124E |
unknown |
Het |
Aqp8 |
T |
C |
7: 123,065,922 (GRCm39) |
L239P |
probably damaging |
Het |
Arhgef11 |
A |
G |
3: 87,593,336 (GRCm39) |
E85G |
probably damaging |
Het |
Cacng4 |
T |
A |
11: 107,685,209 (GRCm39) |
I28F |
possibly damaging |
Het |
Cc2d1a |
T |
C |
8: 84,861,599 (GRCm39) |
D741G |
probably damaging |
Het |
Cct8l1 |
T |
A |
5: 25,722,210 (GRCm39) |
N308K |
possibly damaging |
Het |
Cd300ld2 |
CGAACTGTGGATGGCAGAACTGTGGATGTCAGAACTGTGGATGGCAGAACTGTGGATGTCAGAACTGTGGATGGCAGAACTGTGGATGTCAGAACTGTGGATGTCAGAACTGTGGATGGCACAACTGTGCATGGCAGAACTGTGGATGGCACAACTGTGGATGGCAGAACTGTGG |
CGAACTGTGGATGGCAGAACTGTGGATGTCAGAACTGTGGATGGCAGAACTGTGGATGTCAGAACTGTGGATGTCAGAACTGTGGATGGCACAACTGTGCATGGCAGAACTGTGGATGGCACAACTGTGGATGGCAGAACTGTGG |
11: 114,903,257 (GRCm39) |
|
probably benign |
Het |
Chrna5 |
T |
A |
9: 54,905,348 (GRCm39) |
D53E |
probably benign |
Het |
Dap3 |
A |
T |
3: 88,835,514 (GRCm39) |
|
probably null |
Het |
Disp2 |
A |
G |
2: 118,620,489 (GRCm39) |
Y407C |
probably damaging |
Het |
Dnah1 |
A |
G |
14: 31,008,771 (GRCm39) |
M2001T |
probably benign |
Het |
Dysf |
C |
G |
6: 83,996,466 (GRCm39) |
|
probably benign |
Het |
Eif2ak1 |
A |
T |
5: 143,816,264 (GRCm39) |
K187N |
probably damaging |
Het |
Ethe1 |
T |
C |
7: 24,294,496 (GRCm39) |
S100P |
probably damaging |
Het |
Fam186a |
G |
C |
15: 99,842,604 (GRCm39) |
I1213M |
possibly damaging |
Het |
Gbp9 |
A |
G |
5: 105,232,875 (GRCm39) |
F259S |
probably damaging |
Het |
Heatr5b |
G |
A |
17: 79,072,834 (GRCm39) |
H1610Y |
possibly damaging |
Het |
Hk2 |
T |
A |
6: 82,705,747 (GRCm39) |
D852V |
probably benign |
Het |
Hmcn1 |
T |
A |
1: 150,531,570 (GRCm39) |
Q3233L |
possibly damaging |
Het |
Htt |
T |
A |
5: 35,046,791 (GRCm39) |
V2369E |
probably benign |
Het |
Il9 |
C |
A |
13: 56,629,942 (GRCm39) |
E35* |
probably null |
Het |
Itga8 |
A |
T |
2: 12,137,328 (GRCm39) |
C933* |
probably null |
Het |
Jak3 |
A |
G |
8: 72,138,164 (GRCm39) |
K872E |
possibly damaging |
Het |
Kcnmb2 |
A |
C |
3: 32,252,266 (GRCm39) |
M156L |
probably benign |
Het |
Kdm4a |
C |
T |
4: 117,999,480 (GRCm39) |
V981I |
unknown |
Het |
Klhl38 |
A |
T |
15: 58,178,225 (GRCm39) |
*582R |
probably null |
Het |
Map3k19 |
A |
G |
1: 127,751,866 (GRCm39) |
F495S |
probably damaging |
Het |
Mpeg1 |
T |
A |
19: 12,440,443 (GRCm39) |
W634R |
probably damaging |
Het |
Mrpl4 |
T |
A |
9: 20,918,978 (GRCm39) |
Y202N |
possibly damaging |
Het |
Nme8 |
A |
G |
13: 19,859,978 (GRCm39) |
V214A |
probably damaging |
Het |
Or4k36 |
A |
T |
2: 111,146,239 (GRCm39) |
R138S |
possibly damaging |
Het |
Pcdhgb6 |
A |
G |
18: 37,876,451 (GRCm39) |
I386M |
possibly damaging |
Het |
Pitpnm1 |
T |
A |
19: 4,162,356 (GRCm39) |
V1062E |
possibly damaging |
Het |
Plekhm3 |
G |
A |
1: 64,922,355 (GRCm39) |
R607W |
possibly damaging |
Het |
Plppr2 |
TCGCC |
TC |
9: 21,855,727 (GRCm39) |
|
probably benign |
Het |
Prap1 |
C |
A |
7: 139,676,982 (GRCm39) |
H141Q |
probably damaging |
Het |
Prep |
T |
A |
10: 44,971,252 (GRCm39) |
Y187* |
probably null |
Het |
Rergl |
T |
G |
6: 139,478,865 (GRCm39) |
E3A |
probably benign |
Het |
Rnf19a |
A |
T |
15: 36,242,021 (GRCm39) |
S673T |
probably benign |
Het |
Spata31f3 |
TCATTCAACACTTTGGAGAGCTCTGAACTCTGGCCATTCAACACTTTGGAGAGCTCTGAACTCTGGCCATTCAACACTTTGGAGAGCTCTGAACTCTGGTCATTCAACACTTTGG |
TCATTCAACACTTTGGAGAGCTCTGAACTCTGGCCATTCAACACTTTGGAGAGCTCTGAACTCTGGTCATTCAACACTTTGG |
4: 42,871,823 (GRCm39) |
|
probably benign |
Het |
St18 |
G |
A |
1: 6,880,826 (GRCm39) |
E440K |
probably damaging |
Het |
Syne1 |
T |
A |
10: 5,309,074 (GRCm39) |
Q645L |
probably damaging |
Het |
Tmcc1 |
C |
A |
6: 116,111,099 (GRCm39) |
V61L |
|
Het |
Tmcc1 |
A |
T |
6: 116,111,098 (GRCm39) |
V61E |
|
Het |
Tmem135 |
G |
C |
7: 88,797,186 (GRCm39) |
L357V |
probably benign |
Het |
Tmem201 |
C |
A |
4: 149,814,138 (GRCm39) |
R154L |
possibly damaging |
Het |
Tmem71 |
G |
A |
15: 66,410,655 (GRCm39) |
A239V |
possibly damaging |
Het |
Tpgs2 |
A |
G |
18: 25,284,275 (GRCm39) |
W78R |
probably damaging |
Het |
Tssc4 |
T |
C |
7: 142,623,436 (GRCm39) |
V22A |
unknown |
Het |
Ttn |
T |
A |
2: 76,723,128 (GRCm39) |
E6496D |
unknown |
Het |
Ttn |
T |
A |
2: 76,697,539 (GRCm39) |
L227F |
|
Het |
Vps50 |
G |
T |
6: 3,522,338 (GRCm39) |
G169* |
probably null |
Het |
Yy1 |
CGGCGACCACGGCGGCGGCGGGGGCG |
CGGCG |
12: 108,759,506 (GRCm39) |
|
probably benign |
Het |
Zfp407 |
T |
C |
18: 84,361,185 (GRCm39) |
K1703R |
probably benign |
Het |
Zfp616 |
T |
G |
11: 73,976,523 (GRCm39) |
C931G |
probably damaging |
Het |
Zfp949 |
G |
A |
9: 88,451,417 (GRCm39) |
C329Y |
probably damaging |
Het |
Zswim5 |
T |
A |
4: 116,822,887 (GRCm39) |
D452E |
probably benign |
Het |
|
Other mutations in Or8k33 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01937:Or8k33
|
APN |
2 |
86,383,793 (GRCm39) |
missense |
probably benign |
0.34 |
IGL02169:Or8k33
|
APN |
2 |
86,384,226 (GRCm39) |
missense |
probably benign |
0.39 |
IGL02234:Or8k33
|
APN |
2 |
86,383,610 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02530:Or8k33
|
APN |
2 |
86,384,224 (GRCm39) |
missense |
possibly damaging |
0.60 |
R0046:Or8k33
|
UTSW |
2 |
86,383,976 (GRCm39) |
missense |
probably damaging |
1.00 |
R0360:Or8k33
|
UTSW |
2 |
86,384,123 (GRCm39) |
missense |
probably damaging |
1.00 |
R0364:Or8k33
|
UTSW |
2 |
86,384,123 (GRCm39) |
missense |
probably damaging |
1.00 |
R0377:Or8k33
|
UTSW |
2 |
86,383,927 (GRCm39) |
missense |
probably damaging |
1.00 |
R1496:Or8k33
|
UTSW |
2 |
86,384,096 (GRCm39) |
missense |
probably damaging |
1.00 |
R1609:Or8k33
|
UTSW |
2 |
86,383,949 (GRCm39) |
missense |
probably damaging |
1.00 |
R1674:Or8k33
|
UTSW |
2 |
86,384,204 (GRCm39) |
missense |
probably damaging |
0.96 |
R1816:Or8k33
|
UTSW |
2 |
86,384,011 (GRCm39) |
nonsense |
probably null |
|
R2870:Or8k33
|
UTSW |
2 |
86,383,928 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2870:Or8k33
|
UTSW |
2 |
86,383,928 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4387:Or8k33
|
UTSW |
2 |
86,384,298 (GRCm39) |
missense |
probably damaging |
1.00 |
R4915:Or8k33
|
UTSW |
2 |
86,384,399 (GRCm39) |
missense |
probably damaging |
1.00 |
R4924:Or8k33
|
UTSW |
2 |
86,383,853 (GRCm39) |
missense |
probably damaging |
1.00 |
R4987:Or8k33
|
UTSW |
2 |
86,383,579 (GRCm39) |
splice site |
probably null |
0.10 |
R5774:Or8k33
|
UTSW |
2 |
86,384,351 (GRCm39) |
missense |
possibly damaging |
0.68 |
R6305:Or8k33
|
UTSW |
2 |
86,383,839 (GRCm39) |
missense |
possibly damaging |
0.91 |
R6829:Or8k33
|
UTSW |
2 |
86,383,613 (GRCm39) |
nonsense |
probably null |
|
R7152:Or8k33
|
UTSW |
2 |
86,383,673 (GRCm39) |
missense |
probably benign |
0.14 |
R7561:Or8k33
|
UTSW |
2 |
86,383,661 (GRCm39) |
missense |
probably benign |
0.45 |
R7963:Or8k33
|
UTSW |
2 |
86,383,639 (GRCm39) |
missense |
possibly damaging |
0.86 |
R8031:Or8k33
|
UTSW |
2 |
86,384,447 (GRCm39) |
missense |
probably damaging |
1.00 |
R8177:Or8k33
|
UTSW |
2 |
86,383,623 (GRCm39) |
missense |
noncoding transcript |
|
R8349:Or8k33
|
UTSW |
2 |
86,383,980 (GRCm39) |
missense |
probably benign |
0.22 |
R8449:Or8k33
|
UTSW |
2 |
86,383,980 (GRCm39) |
missense |
probably benign |
0.22 |
R8490:Or8k33
|
UTSW |
2 |
86,384,027 (GRCm39) |
missense |
probably benign |
0.06 |
R8787:Or8k33
|
UTSW |
2 |
86,384,297 (GRCm39) |
missense |
probably damaging |
1.00 |
R8801:Or8k33
|
UTSW |
2 |
86,383,727 (GRCm39) |
missense |
probably benign |
0.22 |
R9035:Or8k33
|
UTSW |
2 |
86,384,021 (GRCm39) |
missense |
probably damaging |
0.98 |
R9301:Or8k33
|
UTSW |
2 |
86,383,818 (GRCm39) |
missense |
possibly damaging |
0.91 |
Z1088:Or8k33
|
UTSW |
2 |
86,384,310 (GRCm39) |
missense |
probably benign |
0.40 |
Z1191:Or8k33
|
UTSW |
2 |
86,384,471 (GRCm39) |
start gained |
probably benign |
|
|