Other mutations in this stock |
Total: 97 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
9530002B09Rik |
T |
A |
4: 122,594,970 (GRCm39) |
|
probably benign |
Het |
Abcc2 |
G |
A |
19: 43,810,044 (GRCm39) |
|
probably benign |
Het |
Abcc8 |
C |
G |
7: 45,771,597 (GRCm39) |
G838A |
probably damaging |
Het |
Akr1c21 |
G |
A |
13: 4,631,199 (GRCm39) |
A245T |
probably damaging |
Het |
Anapc15-ps |
T |
C |
10: 95,509,139 (GRCm39) |
E47G |
probably damaging |
Het |
Apoa1 |
A |
G |
9: 46,141,140 (GRCm39) |
T79A |
probably benign |
Het |
Atp6v1b1 |
A |
G |
6: 83,733,903 (GRCm39) |
H378R |
possibly damaging |
Het |
C4b |
A |
G |
17: 34,954,588 (GRCm39) |
|
probably benign |
Het |
Catsperd |
A |
T |
17: 56,969,821 (GRCm39) |
E638D |
probably benign |
Het |
Cckar |
C |
T |
5: 53,863,595 (GRCm39) |
|
probably null |
Het |
Cfap100 |
C |
T |
6: 90,382,321 (GRCm39) |
|
probably benign |
Het |
Chd1 |
G |
T |
17: 15,970,156 (GRCm39) |
G970C |
probably damaging |
Het |
Col14a1 |
A |
G |
15: 55,309,655 (GRCm39) |
|
probably benign |
Het |
Col17a1 |
C |
T |
19: 47,652,263 (GRCm39) |
V698M |
probably damaging |
Het |
Cpeb1 |
T |
C |
7: 81,011,473 (GRCm39) |
D156G |
possibly damaging |
Het |
Cryl1 |
A |
G |
14: 57,541,232 (GRCm39) |
Y151H |
possibly damaging |
Het |
Csmd3 |
C |
A |
15: 47,520,969 (GRCm39) |
V1881L |
probably damaging |
Het |
Ctnnal1 |
C |
T |
4: 56,847,921 (GRCm39) |
A73T |
probably damaging |
Het |
Cyp2c37 |
T |
C |
19: 39,982,950 (GRCm39) |
S180P |
probably damaging |
Het |
Cyp2c54 |
T |
C |
19: 40,060,613 (GRCm39) |
T123A |
possibly damaging |
Het |
Dennd6b |
T |
C |
15: 89,071,417 (GRCm39) |
D304G |
probably damaging |
Het |
Dnmt3l |
T |
C |
10: 77,887,750 (GRCm39) |
|
probably benign |
Het |
Eci1 |
G |
A |
17: 24,652,234 (GRCm39) |
|
probably null |
Het |
Efhc1 |
A |
G |
1: 21,030,412 (GRCm39) |
Y115C |
probably damaging |
Het |
Ern1 |
T |
A |
11: 106,298,004 (GRCm39) |
K706* |
probably null |
Het |
Ghrl |
T |
C |
6: 113,696,299 (GRCm39) |
E31G |
probably damaging |
Het |
Gpr108 |
A |
C |
17: 57,550,101 (GRCm39) |
V179G |
probably benign |
Het |
Henmt1 |
A |
G |
3: 108,865,851 (GRCm39) |
|
probably benign |
Het |
Ift172 |
A |
G |
5: 31,444,011 (GRCm39) |
V69A |
probably damaging |
Het |
Il17ra |
T |
C |
6: 120,453,940 (GRCm39) |
|
probably benign |
Het |
Il17rb |
T |
C |
14: 29,726,304 (GRCm39) |
N95D |
probably benign |
Het |
Il17rb |
G |
T |
14: 29,728,112 (GRCm39) |
|
probably null |
Het |
Iqub |
G |
A |
6: 24,446,154 (GRCm39) |
L757F |
probably benign |
Het |
Itpr1 |
T |
C |
6: 108,355,128 (GRCm39) |
V473A |
probably benign |
Het |
Itpr2 |
T |
G |
6: 146,131,271 (GRCm39) |
N1978H |
probably damaging |
Het |
Klk1b26 |
T |
A |
7: 43,662,151 (GRCm39) |
F3Y |
probably damaging |
Het |
Lars1 |
A |
G |
18: 42,384,428 (GRCm39) |
V50A |
probably benign |
Het |
Lax1 |
G |
T |
1: 133,607,804 (GRCm39) |
H312Q |
probably benign |
Het |
Lctl |
T |
C |
9: 64,029,596 (GRCm39) |
|
probably benign |
Het |
Lrp2 |
T |
A |
2: 69,287,202 (GRCm39) |
D3745V |
probably damaging |
Het |
Lrp2 |
G |
A |
2: 69,290,681 (GRCm39) |
|
probably benign |
Het |
Lvrn |
A |
T |
18: 46,983,533 (GRCm39) |
H92L |
probably benign |
Het |
Marchf1 |
A |
G |
8: 66,871,625 (GRCm39) |
T385A |
probably damaging |
Het |
Marf1 |
C |
T |
16: 13,960,398 (GRCm39) |
A549T |
probably damaging |
Het |
Mbd5 |
T |
C |
2: 49,162,428 (GRCm39) |
V970A |
possibly damaging |
Het |
Mccc1 |
A |
G |
3: 36,017,719 (GRCm39) |
|
probably benign |
Het |
Mpp4 |
A |
T |
1: 59,182,988 (GRCm39) |
|
probably benign |
Het |
Mrnip |
G |
A |
11: 50,090,747 (GRCm39) |
A304T |
probably damaging |
Het |
Muc5b |
T |
C |
7: 141,418,819 (GRCm39) |
S3922P |
possibly damaging |
Het |
Myh3 |
T |
A |
11: 66,987,333 (GRCm39) |
|
probably benign |
Het |
Nbea |
A |
T |
3: 55,944,698 (GRCm39) |
H555Q |
probably damaging |
Het |
Niban3 |
T |
A |
8: 72,055,143 (GRCm39) |
|
probably benign |
Het |
Nlrp9c |
A |
T |
7: 26,070,901 (GRCm39) |
|
probably benign |
Het |
Nmur1 |
A |
T |
1: 86,315,400 (GRCm39) |
V178E |
probably damaging |
Het |
Nod2 |
T |
G |
8: 89,390,406 (GRCm39) |
S238A |
probably benign |
Het |
Ogfod1 |
A |
T |
8: 94,789,651 (GRCm39) |
T451S |
probably damaging |
Het |
Or2d36 |
T |
A |
7: 106,747,394 (GRCm39) |
Y290* |
probably null |
Het |
Or2z8 |
C |
T |
8: 72,812,244 (GRCm39) |
T240M |
probably damaging |
Het |
Or8b8 |
G |
A |
9: 37,809,138 (GRCm39) |
G146D |
probably benign |
Het |
Pcdh20 |
T |
C |
14: 88,706,104 (GRCm39) |
I399V |
probably benign |
Het |
Pdlim1 |
G |
T |
19: 40,232,017 (GRCm39) |
H120Q |
probably damaging |
Het |
Plg |
T |
C |
17: 12,637,968 (GRCm39) |
V798A |
probably damaging |
Het |
Polr2c |
A |
G |
8: 95,584,403 (GRCm39) |
I39V |
possibly damaging |
Het |
Ppfia2 |
C |
A |
10: 106,666,575 (GRCm39) |
|
probably benign |
Het |
Ppp1r3a |
A |
T |
6: 14,719,696 (GRCm39) |
I406N |
probably benign |
Het |
Psg28 |
A |
T |
7: 18,160,098 (GRCm39) |
M366K |
probably benign |
Het |
Rad54b |
T |
C |
4: 11,601,702 (GRCm39) |
I419T |
probably damaging |
Het |
Rnf43 |
A |
G |
11: 87,622,108 (GRCm39) |
Q403R |
possibly damaging |
Het |
Sema6a |
G |
A |
18: 47,423,112 (GRCm39) |
|
probably null |
Het |
Slc28a3 |
A |
G |
13: 58,717,229 (GRCm39) |
|
probably benign |
Het |
Smad2 |
A |
T |
18: 76,422,108 (GRCm39) |
|
probably null |
Het |
Smad4 |
G |
A |
18: 73,791,720 (GRCm39) |
P274S |
probably benign |
Het |
Smchd1 |
A |
T |
17: 71,710,149 (GRCm39) |
V906D |
probably damaging |
Het |
Soat2 |
C |
A |
15: 102,067,188 (GRCm39) |
R320S |
possibly damaging |
Het |
Spata33 |
C |
T |
8: 123,948,626 (GRCm39) |
A57V |
probably damaging |
Het |
Stab1 |
A |
G |
14: 30,865,375 (GRCm39) |
L1814P |
probably benign |
Het |
Stab2 |
T |
C |
10: 86,783,008 (GRCm39) |
K680R |
probably benign |
Het |
Stil |
A |
G |
4: 114,898,369 (GRCm39) |
|
probably null |
Het |
Sympk |
T |
A |
7: 18,780,774 (GRCm39) |
L759H |
probably benign |
Het |
Tet1 |
A |
T |
10: 62,650,325 (GRCm39) |
|
probably null |
Het |
Tfpi2 |
A |
T |
6: 3,965,460 (GRCm39) |
N117K |
probably benign |
Het |
Tle3 |
A |
G |
9: 61,323,943 (GRCm39) |
Y766C |
probably damaging |
Het |
Trpt1 |
C |
A |
19: 6,975,298 (GRCm39) |
|
probably null |
Het |
Tshz1 |
A |
G |
18: 84,034,174 (GRCm39) |
F78S |
possibly damaging |
Het |
Ttc1 |
T |
C |
11: 43,629,635 (GRCm39) |
D177G |
probably damaging |
Het |
Ttc13 |
T |
A |
8: 125,401,140 (GRCm39) |
Y741F |
probably damaging |
Het |
Ulk3 |
C |
T |
9: 57,502,115 (GRCm39) |
S462L |
probably benign |
Het |
Utrn |
C |
T |
10: 12,401,077 (GRCm39) |
|
probably benign |
Het |
V1rd19 |
A |
C |
7: 23,703,010 (GRCm39) |
T159P |
probably damaging |
Het |
Vars1 |
T |
C |
17: 35,230,462 (GRCm39) |
V515A |
possibly damaging |
Het |
Vmn1r85 |
A |
G |
7: 12,818,515 (GRCm39) |
Y210H |
probably benign |
Het |
Vmn2r89 |
A |
G |
14: 51,693,435 (GRCm39) |
T262A |
probably damaging |
Het |
Vps53 |
G |
A |
11: 76,012,405 (GRCm39) |
T209I |
probably benign |
Het |
Wdfy2 |
T |
C |
14: 63,162,582 (GRCm39) |
F95L |
possibly damaging |
Het |
Wwp1 |
G |
T |
4: 19,627,911 (GRCm39) |
S694Y |
probably damaging |
Het |
Zbtb8b |
T |
A |
4: 129,326,463 (GRCm39) |
D201V |
probably damaging |
Het |
Zmym5 |
A |
C |
14: 57,041,908 (GRCm39) |
N123K |
possibly damaging |
Het |
|
Other mutations in Or1e17 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01546:Or1e17
|
APN |
11 |
73,832,020 (GRCm39) |
missense |
probably benign |
|
IGL02290:Or1e17
|
APN |
11 |
73,831,695 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02301:Or1e17
|
APN |
11 |
73,831,894 (GRCm39) |
missense |
possibly damaging |
0.79 |
IGL02303:Or1e17
|
APN |
11 |
73,831,276 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL02510:Or1e17
|
APN |
11 |
73,831,831 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02558:Or1e17
|
APN |
11 |
73,831,651 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02712:Or1e17
|
APN |
11 |
73,831,756 (GRCm39) |
missense |
probably benign |
0.12 |
IGL02795:Or1e17
|
APN |
11 |
73,831,755 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02800:Or1e17
|
APN |
11 |
73,831,942 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03350:Or1e17
|
APN |
11 |
73,831,664 (GRCm39) |
missense |
probably damaging |
0.99 |
R0277:Or1e17
|
UTSW |
11 |
73,831,773 (GRCm39) |
missense |
probably benign |
0.28 |
R0323:Or1e17
|
UTSW |
11 |
73,831,773 (GRCm39) |
missense |
probably benign |
0.28 |
R0333:Or1e17
|
UTSW |
11 |
73,831,593 (GRCm39) |
missense |
possibly damaging |
0.78 |
R0389:Or1e17
|
UTSW |
11 |
73,831,879 (GRCm39) |
missense |
probably benign |
0.12 |
R0723:Or1e17
|
UTSW |
11 |
73,831,096 (GRCm39) |
missense |
probably benign |
0.00 |
R1469:Or1e17
|
UTSW |
11 |
73,831,383 (GRCm39) |
missense |
probably benign |
0.05 |
R1469:Or1e17
|
UTSW |
11 |
73,831,383 (GRCm39) |
missense |
probably benign |
0.05 |
R1900:Or1e17
|
UTSW |
11 |
73,831,486 (GRCm39) |
missense |
possibly damaging |
0.79 |
R2363:Or1e17
|
UTSW |
11 |
73,831,182 (GRCm39) |
missense |
possibly damaging |
0.96 |
R4236:Or1e17
|
UTSW |
11 |
73,831,182 (GRCm39) |
missense |
possibly damaging |
0.96 |
R4630:Or1e17
|
UTSW |
11 |
73,831,822 (GRCm39) |
missense |
probably damaging |
1.00 |
R4717:Or1e17
|
UTSW |
11 |
73,831,641 (GRCm39) |
missense |
possibly damaging |
0.86 |
R4801:Or1e17
|
UTSW |
11 |
73,831,696 (GRCm39) |
missense |
possibly damaging |
0.88 |
R4802:Or1e17
|
UTSW |
11 |
73,831,696 (GRCm39) |
missense |
possibly damaging |
0.88 |
R4964:Or1e17
|
UTSW |
11 |
73,832,028 (GRCm39) |
missense |
probably benign |
0.04 |
R5119:Or1e17
|
UTSW |
11 |
73,831,378 (GRCm39) |
missense |
possibly damaging |
0.76 |
R5470:Or1e17
|
UTSW |
11 |
73,831,696 (GRCm39) |
missense |
probably benign |
0.06 |
R6196:Or1e17
|
UTSW |
11 |
73,831,635 (GRCm39) |
missense |
possibly damaging |
0.86 |
R6551:Or1e17
|
UTSW |
11 |
73,831,129 (GRCm39) |
missense |
probably benign |
0.11 |
R7695:Or1e17
|
UTSW |
11 |
73,831,720 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7979:Or1e17
|
UTSW |
11 |
73,831,401 (GRCm39) |
missense |
probably benign |
0.00 |
R8074:Or1e17
|
UTSW |
11 |
73,831,213 (GRCm39) |
missense |
possibly damaging |
0.78 |
R8834:Or1e17
|
UTSW |
11 |
73,831,164 (GRCm39) |
missense |
possibly damaging |
0.59 |
R9344:Or1e17
|
UTSW |
11 |
73,831,744 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9352:Or1e17
|
UTSW |
11 |
73,831,470 (GRCm39) |
missense |
probably benign |
0.12 |
R9800:Or1e17
|
UTSW |
11 |
73,831,986 (GRCm39) |
missense |
probably benign |
0.01 |
X0065:Or1e17
|
UTSW |
11 |
73,831,150 (GRCm39) |
missense |
possibly damaging |
0.59 |
Z1088:Or1e17
|
UTSW |
11 |
73,831,964 (GRCm39) |
missense |
probably benign |
0.01 |
|