Other mutations in this stock |
Total: 75 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abo |
T |
G |
2: 26,733,855 (GRCm39) |
T115P |
probably damaging |
Het |
Aggf1 |
G |
A |
13: 95,492,921 (GRCm39) |
R563* |
probably null |
Het |
Amdhd1 |
A |
T |
10: 93,370,360 (GRCm39) |
Y159* |
probably null |
Het |
Camp |
T |
C |
9: 109,677,461 (GRCm39) |
E124G |
|
Het |
Casq2 |
A |
G |
3: 101,994,016 (GRCm39) |
E21G |
possibly damaging |
Het |
Cbln1 |
A |
T |
8: 88,198,357 (GRCm39) |
F116Y |
probably damaging |
Het |
Cklf |
A |
T |
8: 104,989,996 (GRCm39) |
K143* |
probably null |
Het |
Clca3a1 |
A |
G |
3: 144,457,723 (GRCm39) |
I387T |
probably damaging |
Het |
Cndp1 |
T |
A |
18: 84,654,174 (GRCm39) |
D130V |
probably benign |
Het |
Cyp4a12a |
T |
A |
4: 115,184,670 (GRCm39) |
M317K |
possibly damaging |
Het |
Dmxl2 |
A |
T |
9: 54,365,078 (GRCm39) |
I138K |
unknown |
Het |
Eapp |
A |
G |
12: 54,720,508 (GRCm39) |
S236P |
probably benign |
Het |
Efcab3 |
T |
A |
11: 104,927,625 (GRCm39) |
M4798K |
probably benign |
Het |
Efnb3 |
T |
C |
11: 69,448,046 (GRCm39) |
H132R |
possibly damaging |
Het |
Fam243 |
A |
G |
16: 92,117,805 (GRCm39) |
V161A |
probably damaging |
Het |
Fbn2 |
A |
T |
18: 58,238,208 (GRCm39) |
N596K |
probably damaging |
Het |
Fzd9 |
A |
G |
5: 135,279,484 (GRCm39) |
W134R |
probably damaging |
Het |
Gga2 |
A |
G |
7: 121,603,157 (GRCm39) |
S180P |
probably damaging |
Het |
Golga3 |
A |
G |
5: 110,353,694 (GRCm39) |
T911A |
probably benign |
Het |
Gstm1 |
C |
T |
3: 107,921,866 (GRCm39) |
|
probably null |
Het |
Heg1 |
A |
G |
16: 33,547,867 (GRCm39) |
T909A |
probably damaging |
Het |
Herc2 |
T |
C |
7: 55,807,186 (GRCm39) |
S2455P |
probably benign |
Het |
Herc2 |
C |
T |
7: 55,870,273 (GRCm39) |
R4349W |
probably damaging |
Het |
Hivep2 |
T |
G |
10: 14,019,595 (GRCm39) |
M2122R |
possibly damaging |
Het |
Itga10 |
T |
A |
3: 96,564,707 (GRCm39) |
|
probably null |
Het |
Kbtbd13 |
G |
T |
9: 65,298,605 (GRCm39) |
C110* |
probably null |
Het |
Krt78 |
T |
C |
15: 101,859,318 (GRCm39) |
E293G |
probably damaging |
Het |
Lgals3bp |
C |
T |
11: 118,288,995 (GRCm39) |
V110M |
possibly damaging |
Het |
Lrp2 |
A |
G |
2: 69,307,352 (GRCm39) |
|
probably null |
Het |
Lrrc14 |
A |
G |
15: 76,598,173 (GRCm39) |
D301G |
probably benign |
Het |
Lrrc71 |
C |
A |
3: 87,649,113 (GRCm39) |
G352W |
probably damaging |
Het |
Map3k9 |
A |
G |
12: 81,771,506 (GRCm39) |
V694A |
probably benign |
Het |
Mboat2 |
T |
C |
12: 24,989,325 (GRCm39) |
S162P |
probably damaging |
Het |
Megf11 |
C |
A |
9: 64,586,535 (GRCm39) |
N422K |
probably damaging |
Het |
Miga1 |
C |
T |
3: 151,982,324 (GRCm39) |
S584N |
probably benign |
Het |
Mindy2 |
A |
G |
9: 70,524,141 (GRCm39) |
Y403H |
probably damaging |
Het |
Mmd |
C |
T |
11: 90,167,583 (GRCm39) |
A204V |
possibly damaging |
Het |
Mta3 |
A |
T |
17: 84,107,572 (GRCm39) |
Y262F |
probably benign |
Het |
Ncoa7 |
G |
A |
10: 30,598,794 (GRCm39) |
S43F |
probably benign |
Het |
Nhsl3 |
T |
C |
4: 129,115,734 (GRCm39) |
T1022A |
probably benign |
Het |
Nphp4 |
T |
C |
4: 152,638,991 (GRCm39) |
V874A |
probably benign |
Het |
Nsd1 |
A |
G |
13: 55,460,141 (GRCm39) |
T2226A |
probably benign |
Het |
Nt5dc1 |
T |
C |
10: 34,190,792 (GRCm39) |
H302R |
probably benign |
Het |
Odc1 |
A |
G |
12: 17,600,003 (GRCm39) |
Y389C |
probably damaging |
Het |
Or52p2 |
A |
G |
7: 102,237,125 (GRCm39) |
I275T |
probably damaging |
Het |
Or5k8 |
G |
A |
16: 58,644,958 (GRCm39) |
T38I |
probably damaging |
Het |
Pcare |
T |
C |
17: 72,057,880 (GRCm39) |
D599G |
probably damaging |
Het |
Pcdhb10 |
A |
C |
18: 37,545,365 (GRCm39) |
Q147P |
probably benign |
Het |
Pdcl2 |
A |
C |
5: 76,465,675 (GRCm39) |
C182G |
probably damaging |
Het |
Pigv |
T |
C |
4: 133,392,762 (GRCm39) |
D136G |
possibly damaging |
Het |
Polr1h |
A |
C |
17: 37,268,722 (GRCm39) |
|
probably null |
Het |
Pramel5 |
T |
C |
4: 143,998,010 (GRCm39) |
E411G |
possibly damaging |
Het |
Prkce |
T |
C |
17: 86,476,028 (GRCm39) |
V3A |
probably benign |
Het |
Pth1r |
T |
C |
9: 110,551,461 (GRCm39) |
N546S |
probably benign |
Het |
Qrich2 |
C |
T |
11: 116,346,148 (GRCm39) |
V1559I |
probably benign |
Het |
Rbm20 |
A |
C |
19: 53,802,764 (GRCm39) |
D424A |
possibly damaging |
Het |
Rbm26 |
C |
T |
14: 105,388,284 (GRCm39) |
D393N |
probably damaging |
Het |
Sf3b3 |
G |
A |
8: 111,547,445 (GRCm39) |
R728C |
probably damaging |
Het |
Spata31e1 |
G |
T |
13: 49,940,451 (GRCm39) |
Q420K |
probably benign |
Het |
Srcap |
A |
G |
7: 127,137,920 (GRCm39) |
N1090S |
probably benign |
Het |
Syt4 |
A |
T |
18: 31,576,875 (GRCm39) |
S160T |
probably benign |
Het |
Tcstv6 |
A |
T |
13: 120,304,224 (GRCm39) |
|
probably null |
Het |
Tfap2e |
C |
T |
4: 126,615,727 (GRCm39) |
V236M |
probably damaging |
Het |
Thsd4 |
G |
A |
9: 60,301,755 (GRCm39) |
T180M |
probably damaging |
Het |
Tlr4 |
T |
A |
4: 66,758,443 (GRCm39) |
M412K |
probably damaging |
Het |
Tmem67 |
T |
A |
4: 12,079,883 (GRCm39) |
H136L |
probably benign |
Het |
Tnpo2 |
T |
A |
8: 85,771,044 (GRCm39) |
I110N |
probably benign |
Het |
Trav13d-3 |
A |
G |
14: 53,270,870 (GRCm39) |
M111V |
probably benign |
Het |
Tubb3 |
A |
T |
8: 124,147,900 (GRCm39) |
S278C |
probably benign |
Het |
Ugcg |
T |
A |
4: 59,220,299 (GRCm39) |
F364Y |
probably benign |
Het |
Usp17lc |
T |
C |
7: 103,067,706 (GRCm39) |
S334P |
probably damaging |
Het |
Vps13c |
A |
G |
9: 67,852,791 (GRCm39) |
D2357G |
probably damaging |
Het |
Zfp157 |
T |
C |
5: 138,454,172 (GRCm39) |
Y125H |
probably benign |
Het |
Zfp747 |
A |
T |
7: 126,973,819 (GRCm39) |
M117K |
probably benign |
Het |
Zscan4c |
A |
T |
7: 10,743,658 (GRCm39) |
N419I |
possibly damaging |
Het |
|
Other mutations in Or8g37 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01388:Or8g37
|
APN |
9 |
39,731,298 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02674:Or8g37
|
APN |
9 |
39,730,934 (GRCm39) |
splice site |
probably null |
|
R0659:Or8g37
|
UTSW |
9 |
39,731,112 (GRCm39) |
missense |
possibly damaging |
0.78 |
R0686:Or8g37
|
UTSW |
9 |
39,730,964 (GRCm39) |
missense |
probably damaging |
0.98 |
R1952:Or8g37
|
UTSW |
9 |
39,731,363 (GRCm39) |
missense |
probably benign |
0.09 |
R2068:Or8g37
|
UTSW |
9 |
39,731,846 (GRCm39) |
missense |
probably benign |
0.00 |
R4472:Or8g37
|
UTSW |
9 |
39,731,870 (GRCm39) |
makesense |
probably null |
|
R4798:Or8g37
|
UTSW |
9 |
39,731,193 (GRCm39) |
missense |
probably benign |
0.13 |
R5035:Or8g37
|
UTSW |
9 |
39,731,390 (GRCm39) |
missense |
possibly damaging |
0.82 |
R5339:Or8g37
|
UTSW |
9 |
39,731,229 (GRCm39) |
missense |
probably damaging |
0.97 |
R6751:Or8g37
|
UTSW |
9 |
39,731,193 (GRCm39) |
missense |
probably benign |
0.13 |
R7211:Or8g37
|
UTSW |
9 |
39,731,154 (GRCm39) |
missense |
possibly damaging |
0.76 |
R7471:Or8g37
|
UTSW |
9 |
39,731,423 (GRCm39) |
missense |
probably benign |
0.00 |
R7609:Or8g37
|
UTSW |
9 |
39,731,583 (GRCm39) |
missense |
probably benign |
|
R7890:Or8g37
|
UTSW |
9 |
39,731,310 (GRCm39) |
missense |
probably damaging |
0.99 |
R7918:Or8g37
|
UTSW |
9 |
39,731,406 (GRCm39) |
missense |
probably damaging |
0.98 |
R8548:Or8g37
|
UTSW |
9 |
39,731,537 (GRCm39) |
missense |
probably benign |
0.00 |
R8817:Or8g37
|
UTSW |
9 |
39,730,939 (GRCm39) |
start codon destroyed |
probably null |
0.40 |
R8868:Or8g37
|
UTSW |
9 |
39,731,252 (GRCm39) |
missense |
probably benign |
|
R9689:Or8g37
|
UTSW |
9 |
39,731,801 (GRCm39) |
missense |
possibly damaging |
0.95 |
Z1176:Or8g37
|
UTSW |
9 |
39,731,651 (GRCm39) |
missense |
probably damaging |
1.00 |
|