Other mutations in this stock |
Total: 76 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ace |
A |
G |
11: 105,870,445 (GRCm39) |
H288R |
possibly damaging |
Het |
Adh1 |
T |
C |
3: 137,995,565 (GRCm39) |
F323L |
probably benign |
Het |
Adss1 |
A |
C |
12: 112,600,837 (GRCm39) |
H226P |
probably damaging |
Het |
Ahrr |
A |
G |
13: 74,371,031 (GRCm39) |
S230P |
possibly damaging |
Het |
Akap9 |
T |
C |
5: 4,012,105 (GRCm39) |
V936A |
probably damaging |
Het |
B4galnt2 |
A |
G |
11: 95,759,268 (GRCm39) |
Y339H |
probably damaging |
Het |
Bltp1 |
T |
C |
3: 37,002,453 (GRCm39) |
V1466A |
probably damaging |
Het |
C4b |
C |
A |
17: 34,957,848 (GRCm39) |
G611V |
possibly damaging |
Het |
Cacna1i |
A |
G |
15: 80,205,427 (GRCm39) |
M128V |
probably damaging |
Het |
Chia1 |
T |
C |
3: 106,038,213 (GRCm39) |
S370P |
possibly damaging |
Het |
Cops6 |
T |
C |
5: 138,159,673 (GRCm39) |
V9A |
possibly damaging |
Het |
D630003M21Rik |
A |
T |
2: 158,059,321 (GRCm39) |
I193K |
probably benign |
Het |
Daam2 |
T |
C |
17: 49,801,467 (GRCm39) |
D90G |
probably damaging |
Het |
Fads3 |
A |
G |
19: 10,019,202 (GRCm39) |
D36G |
probably benign |
Het |
Fam185a |
T |
C |
5: 21,630,554 (GRCm39) |
V130A |
probably damaging |
Het |
Fbn1 |
A |
T |
2: 125,172,463 (GRCm39) |
N1928K |
probably damaging |
Het |
Fstl3 |
A |
G |
10: 79,615,843 (GRCm39) |
M110V |
probably benign |
Het |
G2e3 |
A |
G |
12: 51,415,919 (GRCm39) |
T552A |
possibly damaging |
Het |
Gfra1 |
G |
A |
19: 58,226,830 (GRCm39) |
T462I |
probably damaging |
Het |
Glrx2 |
T |
A |
1: 143,621,121 (GRCm39) |
|
probably benign |
Het |
Gm10100 |
G |
T |
10: 77,562,498 (GRCm39) |
C60F |
possibly damaging |
Het |
Gm43302 |
T |
A |
5: 105,425,605 (GRCm39) |
K275* |
probably null |
Het |
Gm6569 |
A |
G |
15: 73,711,640 (GRCm39) |
|
probably benign |
Het |
Herc6 |
G |
T |
6: 57,639,139 (GRCm39) |
V867L |
possibly damaging |
Het |
Hhipl2 |
T |
A |
1: 183,209,459 (GRCm39) |
|
probably null |
Het |
Kcnj16 |
A |
T |
11: 110,916,378 (GRCm39) |
K347* |
probably null |
Het |
Kcnt2 |
T |
A |
1: 140,354,661 (GRCm39) |
C305* |
probably null |
Het |
Large2 |
A |
G |
2: 92,196,825 (GRCm39) |
L477P |
probably damaging |
Het |
Lnpep |
T |
C |
17: 17,799,245 (GRCm39) |
T137A |
possibly damaging |
Het |
Mettl3 |
T |
C |
14: 52,534,215 (GRCm39) |
|
probably null |
Het |
Mical3 |
C |
T |
6: 120,935,684 (GRCm39) |
S1614N |
probably damaging |
Het |
Mmut |
T |
A |
17: 41,249,622 (GRCm39) |
V199E |
possibly damaging |
Het |
Morc3 |
C |
A |
16: 93,642,082 (GRCm39) |
Y100* |
probably null |
Het |
Mrc2 |
A |
G |
11: 105,237,646 (GRCm39) |
K1108R |
probably benign |
Het |
Mrpl2 |
T |
C |
17: 46,960,835 (GRCm39) |
V243A |
probably damaging |
Het |
Mtor |
T |
A |
4: 148,605,794 (GRCm39) |
N1505K |
probably benign |
Het |
Myo1g |
A |
T |
11: 6,469,168 (GRCm39) |
Y45N |
probably damaging |
Het |
Nckap5l |
C |
A |
15: 99,325,905 (GRCm39) |
L199F |
possibly damaging |
Het |
Ndufc2 |
A |
G |
7: 97,056,099 (GRCm39) |
T66A |
probably damaging |
Het |
Nos1 |
T |
A |
5: 118,050,917 (GRCm39) |
H779Q |
probably damaging |
Het |
Or13j1 |
T |
C |
4: 43,705,698 (GRCm39) |
Y290C |
probably damaging |
Het |
Or1e23 |
T |
C |
11: 73,407,831 (GRCm39) |
N65D |
probably damaging |
Het |
Or4c3 |
A |
G |
2: 89,851,573 (GRCm39) |
|
probably null |
Het |
Or51ah3 |
A |
T |
7: 103,210,489 (GRCm39) |
R268S |
probably benign |
Het |
Or5au1 |
C |
A |
14: 52,272,825 (GRCm39) |
V248L |
possibly damaging |
Het |
Or5k16 |
T |
C |
16: 58,736,545 (GRCm39) |
N153S |
probably benign |
Het |
Otog |
C |
T |
7: 45,898,458 (GRCm39) |
T192I |
possibly damaging |
Het |
Oxct1 |
T |
C |
15: 4,064,812 (GRCm39) |
V50A |
probably benign |
Het |
P3h2 |
T |
A |
16: 25,784,493 (GRCm39) |
D667V |
probably damaging |
Het |
Pcdhb20 |
A |
G |
18: 37,638,047 (GRCm39) |
Y191C |
probably damaging |
Het |
Pds5b |
T |
G |
5: 150,670,083 (GRCm39) |
V357G |
probably damaging |
Het |
Pggt1b |
A |
G |
18: 46,407,674 (GRCm39) |
V81A |
possibly damaging |
Het |
Phxr2 |
A |
G |
10: 98,962,043 (GRCm39) |
|
probably benign |
Het |
Pnpt1 |
T |
C |
11: 29,095,469 (GRCm39) |
I406T |
probably benign |
Het |
Ppat |
T |
C |
5: 77,070,202 (GRCm39) |
I173V |
probably damaging |
Het |
Proser3 |
T |
C |
7: 30,243,153 (GRCm39) |
S167G |
probably damaging |
Het |
Rnf135 |
A |
C |
11: 80,080,053 (GRCm39) |
T115P |
possibly damaging |
Het |
Rpl22 |
C |
T |
4: 152,414,536 (GRCm39) |
R65C |
probably benign |
Het |
Scel |
T |
C |
14: 103,829,420 (GRCm39) |
F405L |
probably benign |
Het |
Serinc3 |
A |
G |
2: 163,469,799 (GRCm39) |
Y350H |
probably damaging |
Het |
Slc25a16 |
C |
A |
10: 62,764,102 (GRCm39) |
T53K |
probably damaging |
Het |
Slco1a1 |
A |
T |
6: 141,870,215 (GRCm39) |
F308I |
possibly damaging |
Het |
Slitrk5 |
GACTAC |
GACTACTAC |
14: 111,917,248 (GRCm39) |
|
probably benign |
Het |
Smok3c |
T |
C |
5: 138,063,314 (GRCm39) |
V267A |
probably benign |
Het |
Ssrp1 |
A |
G |
2: 84,873,158 (GRCm39) |
D473G |
probably benign |
Het |
Svs6 |
A |
G |
2: 164,159,405 (GRCm39) |
E56G |
possibly damaging |
Het |
Tas2r130 |
TCATTTC |
T |
6: 131,607,547 (GRCm39) |
|
probably benign |
Het |
Thoc3 |
T |
C |
13: 54,615,785 (GRCm39) |
N93S |
probably benign |
Het |
Tle6 |
A |
G |
10: 81,428,600 (GRCm39) |
C443R |
probably damaging |
Het |
Tmed6 |
A |
G |
8: 107,788,371 (GRCm39) |
F192S |
probably damaging |
Het |
Tpx2 |
A |
G |
2: 152,718,548 (GRCm39) |
N184D |
probably benign |
Het |
Vmn2r31 |
T |
A |
7: 7,397,638 (GRCm39) |
N207Y |
probably benign |
Het |
Zfp267 |
T |
C |
3: 36,220,352 (GRCm39) |
F792L |
probably benign |
Het |
Zfp709 |
TCGACG |
TCG |
8: 72,644,552 (GRCm39) |
|
probably benign |
Het |
Zfp972 |
A |
T |
2: 177,549,117 (GRCm39) |
|
probably null |
Het |
Zzef1 |
G |
A |
11: 72,760,631 (GRCm39) |
C1318Y |
possibly damaging |
Het |
|
Other mutations in Or12e13 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01727:Or12e13
|
APN |
2 |
87,663,844 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01893:Or12e13
|
APN |
2 |
87,664,207 (GRCm39) |
nonsense |
probably null |
|
IGL02247:Or12e13
|
APN |
2 |
87,663,873 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02286:Or12e13
|
APN |
2 |
87,663,592 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02645:Or12e13
|
APN |
2 |
87,663,959 (GRCm39) |
missense |
probably benign |
0.21 |
R1304:Or12e13
|
UTSW |
2 |
87,664,049 (GRCm39) |
missense |
possibly damaging |
0.51 |
R1762:Or12e13
|
UTSW |
2 |
87,664,009 (GRCm39) |
missense |
probably damaging |
0.98 |
R1770:Or12e13
|
UTSW |
2 |
87,663,643 (GRCm39) |
missense |
probably benign |
0.05 |
R4308:Or12e13
|
UTSW |
2 |
87,663,614 (GRCm39) |
missense |
probably damaging |
0.99 |
R4721:Or12e13
|
UTSW |
2 |
87,663,515 (GRCm39) |
missense |
probably damaging |
1.00 |
R6011:Or12e13
|
UTSW |
2 |
87,664,259 (GRCm39) |
missense |
probably damaging |
1.00 |
R6243:Or12e13
|
UTSW |
2 |
87,663,385 (GRCm39) |
start codon destroyed |
probably null |
0.00 |
R6367:Or12e13
|
UTSW |
2 |
87,663,937 (GRCm39) |
missense |
probably damaging |
1.00 |
R7379:Or12e13
|
UTSW |
2 |
87,664,123 (GRCm39) |
missense |
probably damaging |
1.00 |
R7510:Or12e13
|
UTSW |
2 |
87,663,872 (GRCm39) |
missense |
probably damaging |
0.97 |
R7967:Or12e13
|
UTSW |
2 |
87,663,863 (GRCm39) |
missense |
possibly damaging |
0.76 |
R8003:Or12e13
|
UTSW |
2 |
87,664,081 (GRCm39) |
missense |
probably benign |
0.00 |
R8177:Or12e13
|
UTSW |
2 |
87,663,512 (GRCm39) |
missense |
probably benign |
0.07 |
R8986:Or12e13
|
UTSW |
2 |
87,663,655 (GRCm39) |
missense |
possibly damaging |
0.71 |
R9149:Or12e13
|
UTSW |
2 |
87,663,523 (GRCm39) |
nonsense |
probably null |
|
R9308:Or12e13
|
UTSW |
2 |
87,663,523 (GRCm39) |
missense |
probably damaging |
1.00 |
R9489:Or12e13
|
UTSW |
2 |
87,663,478 (GRCm39) |
missense |
probably benign |
0.04 |
R9605:Or12e13
|
UTSW |
2 |
87,663,478 (GRCm39) |
missense |
probably benign |
0.04 |
R9740:Or12e13
|
UTSW |
2 |
87,663,895 (GRCm39) |
missense |
probably damaging |
1.00 |
X0050:Or12e13
|
UTSW |
2 |
87,663,878 (GRCm39) |
frame shift |
probably null |
|
|