Other mutations in this stock |
Total: 68 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4933421I07Rik |
C |
A |
7: 42,095,667 (GRCm39) |
G194C |
possibly damaging |
Het |
Adamtsl1 |
A |
G |
4: 86,135,248 (GRCm39) |
K258E |
probably damaging |
Het |
Afdn |
A |
T |
17: 14,030,707 (GRCm39) |
D206V |
possibly damaging |
Het |
Agt |
G |
T |
8: 125,284,572 (GRCm39) |
Q389K |
possibly damaging |
Het |
Ankrd44 |
A |
T |
1: 54,801,432 (GRCm39) |
D298E |
probably damaging |
Het |
Anks1 |
A |
G |
17: 28,271,709 (GRCm39) |
S897G |
probably benign |
Het |
Apol9b |
A |
G |
15: 77,619,746 (GRCm39) |
|
probably null |
Het |
Baz1a |
T |
C |
12: 54,965,339 (GRCm39) |
E705G |
probably benign |
Het |
BC048679 |
C |
T |
7: 81,144,966 (GRCm39) |
V126M |
probably benign |
Het |
Cep295 |
A |
G |
9: 15,246,210 (GRCm39) |
F749L |
possibly damaging |
Het |
Cntrl |
T |
A |
2: 35,018,036 (GRCm39) |
I482K |
possibly damaging |
Het |
Col6a3 |
A |
G |
1: 90,749,955 (GRCm39) |
F293S |
probably damaging |
Het |
Dnah12 |
T |
G |
14: 26,439,129 (GRCm39) |
M527R |
probably damaging |
Het |
Dnhd1 |
G |
A |
7: 105,343,273 (GRCm39) |
R1539H |
probably benign |
Het |
Ece1 |
A |
G |
4: 137,685,319 (GRCm39) |
Y603C |
probably damaging |
Het |
Eea1 |
G |
A |
10: 95,877,335 (GRCm39) |
A1350T |
possibly damaging |
Het |
Exoc3l4 |
A |
T |
12: 111,394,402 (GRCm39) |
K507N |
possibly damaging |
Het |
Flt3l |
A |
T |
7: 44,783,091 (GRCm39) |
|
probably null |
Het |
Fn1 |
T |
C |
1: 71,667,230 (GRCm39) |
Q834R |
probably benign |
Het |
Haus5 |
C |
T |
7: 30,358,401 (GRCm39) |
W298* |
probably null |
Het |
Hycc2 |
T |
A |
1: 58,569,034 (GRCm39) |
Y515F |
probably damaging |
Het |
Ifih1 |
T |
C |
2: 62,469,827 (GRCm39) |
N157D |
possibly damaging |
Het |
Itga2 |
A |
C |
13: 114,980,009 (GRCm39) |
M1064R |
probably benign |
Het |
Itgae |
A |
G |
11: 73,002,228 (GRCm39) |
|
probably null |
Het |
Krtap10-4 |
T |
C |
10: 77,662,883 (GRCm39) |
|
probably benign |
Het |
Lamp3 |
A |
G |
16: 19,518,431 (GRCm39) |
C269R |
probably damaging |
Het |
Lrp5 |
T |
C |
19: 3,709,355 (GRCm39) |
D125G |
probably damaging |
Het |
Matn2 |
A |
C |
15: 34,423,901 (GRCm39) |
E586D |
probably benign |
Het |
Mef2b |
T |
A |
8: 70,616,789 (GRCm39) |
|
probably null |
Het |
Mrps22 |
A |
G |
9: 98,483,524 (GRCm39) |
|
probably null |
Het |
Mtmr2 |
T |
C |
9: 13,711,325 (GRCm39) |
F445L |
probably damaging |
Het |
Nxph4 |
A |
G |
10: 127,362,237 (GRCm39) |
V218A |
probably damaging |
Het |
Or1e23 |
A |
G |
11: 73,408,001 (GRCm39) |
V8A |
probably benign |
Het |
Or4f57 |
C |
T |
2: 111,791,091 (GRCm39) |
G109D |
probably damaging |
Het |
Pdpk1 |
A |
T |
17: 24,325,896 (GRCm39) |
V100D |
probably damaging |
Het |
Phldb2 |
A |
C |
16: 45,594,609 (GRCm39) |
S899A |
probably benign |
Het |
Pnpla3 |
G |
A |
15: 84,056,983 (GRCm39) |
|
probably null |
Het |
Rasal2 |
A |
G |
1: 157,126,757 (GRCm39) |
Y94H |
probably damaging |
Het |
Rlf |
A |
T |
4: 121,006,019 (GRCm39) |
I987N |
possibly damaging |
Het |
Rnd2 |
C |
T |
11: 101,359,825 (GRCm39) |
L57F |
probably damaging |
Het |
Rprd2 |
A |
G |
3: 95,687,753 (GRCm39) |
Y300H |
probably damaging |
Het |
Setbp1 |
G |
A |
18: 78,826,584 (GRCm39) |
S1343L |
probably benign |
Het |
Sfswap |
A |
G |
5: 129,648,105 (GRCm39) |
K938E |
possibly damaging |
Het |
Shld2 |
A |
G |
14: 33,990,129 (GRCm39) |
V259A |
probably benign |
Het |
Slc3a1 |
A |
C |
17: 85,335,860 (GRCm39) |
M1L |
probably damaging |
Het |
Slco5a1 |
C |
T |
1: 12,991,409 (GRCm39) |
V427I |
probably benign |
Het |
Ssbp2 |
A |
T |
13: 91,839,027 (GRCm39) |
M300L |
probably benign |
Het |
Ssc5d |
A |
G |
7: 4,940,521 (GRCm39) |
D878G |
probably damaging |
Het |
Stk19 |
A |
G |
17: 35,043,574 (GRCm39) |
L212P |
probably damaging |
Het |
Stk39 |
T |
C |
2: 68,240,387 (GRCm39) |
M115V |
possibly damaging |
Het |
Syt17 |
A |
C |
7: 118,033,466 (GRCm39) |
S181A |
probably benign |
Het |
Taar7b |
A |
T |
10: 23,875,849 (GRCm39) |
N5Y |
probably benign |
Het |
Tmc4 |
A |
G |
7: 3,680,421 (GRCm39) |
|
probably null |
Het |
Tmem248 |
T |
A |
5: 130,258,310 (GRCm39) |
M1K |
probably null |
Het |
Tmem82 |
T |
A |
4: 141,343,721 (GRCm39) |
Q183L |
probably damaging |
Het |
Tpd52l1 |
T |
C |
10: 31,214,203 (GRCm39) |
E142G |
probably damaging |
Het |
Ttll2 |
A |
T |
17: 7,619,167 (GRCm39) |
H253Q |
probably damaging |
Het |
Ttn |
T |
C |
2: 76,687,808 (GRCm39) |
|
probably benign |
Het |
Ubd |
A |
G |
17: 37,506,392 (GRCm39) |
K93E |
probably benign |
Het |
Ugt2b35 |
T |
A |
5: 87,149,415 (GRCm39) |
F222Y |
probably damaging |
Het |
Vmn2r10 |
G |
T |
5: 109,151,328 (GRCm39) |
N95K |
probably damaging |
Het |
Vwa8 |
T |
C |
14: 79,434,904 (GRCm39) |
V1775A |
probably benign |
Het |
Zdbf2 |
A |
G |
1: 63,346,981 (GRCm39) |
K1787E |
possibly damaging |
Het |
Zfp26 |
A |
T |
9: 20,348,582 (GRCm39) |
F661I |
probably damaging |
Het |
Zfp735 |
A |
T |
11: 73,602,504 (GRCm39) |
K483* |
probably null |
Het |
Zfp946 |
A |
G |
17: 22,673,519 (GRCm39) |
E91G |
probably damaging |
Het |
Zic5 |
C |
A |
14: 122,697,161 (GRCm39) |
D485Y |
unknown |
Het |
Zmynd8 |
A |
T |
2: 165,680,772 (GRCm39) |
D236E |
probably damaging |
Het |
|
Other mutations in Or51k1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01096:Or51k1
|
APN |
7 |
103,661,321 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01547:Or51k1
|
APN |
7 |
103,661,867 (GRCm39) |
missense |
probably benign |
0.43 |
IGL02173:Or51k1
|
APN |
7 |
103,661,037 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02707:Or51k1
|
APN |
7 |
103,661,609 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03124:Or51k1
|
APN |
7 |
103,661,001 (GRCm39) |
missense |
probably benign |
|
R0004:Or51k1
|
UTSW |
7 |
103,661,638 (GRCm39) |
missense |
probably benign |
0.02 |
R0086:Or51k1
|
UTSW |
7 |
103,661,261 (GRCm39) |
missense |
probably benign |
0.23 |
R0370:Or51k1
|
UTSW |
7 |
103,661,266 (GRCm39) |
missense |
probably damaging |
0.99 |
R0599:Or51k1
|
UTSW |
7 |
103,661,395 (GRCm39) |
nonsense |
probably null |
|
R1351:Or51k1
|
UTSW |
7 |
103,661,523 (GRCm39) |
missense |
possibly damaging |
0.81 |
R1604:Or51k1
|
UTSW |
7 |
103,661,162 (GRCm39) |
missense |
probably damaging |
1.00 |
R2314:Or51k1
|
UTSW |
7 |
103,661,436 (GRCm39) |
missense |
probably benign |
0.09 |
R2656:Or51k1
|
UTSW |
7 |
103,661,072 (GRCm39) |
missense |
probably damaging |
0.96 |
R4594:Or51k1
|
UTSW |
7 |
103,661,624 (GRCm39) |
missense |
probably benign |
0.01 |
R4774:Or51k1
|
UTSW |
7 |
103,661,795 (GRCm39) |
missense |
probably benign |
0.00 |
R4945:Or51k1
|
UTSW |
7 |
103,661,585 (GRCm39) |
missense |
possibly damaging |
0.85 |
R4968:Or51k1
|
UTSW |
7 |
103,661,777 (GRCm39) |
missense |
probably damaging |
1.00 |
R4981:Or51k1
|
UTSW |
7 |
103,661,312 (GRCm39) |
missense |
probably damaging |
0.97 |
R5072:Or51k1
|
UTSW |
7 |
103,661,325 (GRCm39) |
missense |
probably damaging |
0.97 |
R5982:Or51k1
|
UTSW |
7 |
103,661,117 (GRCm39) |
missense |
probably damaging |
1.00 |
R6303:Or51k1
|
UTSW |
7 |
103,661,238 (GRCm39) |
missense |
probably damaging |
1.00 |
R6304:Or51k1
|
UTSW |
7 |
103,661,238 (GRCm39) |
missense |
probably damaging |
1.00 |
R7107:Or51k1
|
UTSW |
7 |
103,661,489 (GRCm39) |
missense |
probably benign |
0.16 |
R7152:Or51k1
|
UTSW |
7 |
103,661,226 (GRCm39) |
missense |
probably benign |
|
R7456:Or51k1
|
UTSW |
7 |
103,661,045 (GRCm39) |
missense |
possibly damaging |
0.83 |
R7849:Or51k1
|
UTSW |
7 |
103,661,510 (GRCm39) |
missense |
possibly damaging |
0.56 |
R8023:Or51k1
|
UTSW |
7 |
103,661,006 (GRCm39) |
missense |
probably damaging |
0.97 |
R8082:Or51k1
|
UTSW |
7 |
103,661,897 (GRCm39) |
missense |
probably benign |
0.04 |
R8215:Or51k1
|
UTSW |
7 |
103,661,330 (GRCm39) |
missense |
possibly damaging |
0.85 |
R8428:Or51k1
|
UTSW |
7 |
103,661,632 (GRCm39) |
nonsense |
probably null |
|
R8985:Or51k1
|
UTSW |
7 |
103,661,367 (GRCm39) |
missense |
probably damaging |
1.00 |
R9261:Or51k1
|
UTSW |
7 |
103,661,336 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Or51k1
|
UTSW |
7 |
103,661,357 (GRCm39) |
nonsense |
probably null |
|
|