Other mutations in this stock |
Total: 82 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acp7 |
G |
T |
7: 28,314,877 (GRCm39) |
R239S |
possibly damaging |
Het |
Angptl1 |
C |
A |
1: 156,684,735 (GRCm39) |
N301K |
probably benign |
Het |
Ankrd26 |
T |
A |
6: 118,509,257 (GRCm39) |
T603S |
probably benign |
Het |
App |
T |
C |
16: 84,853,322 (GRCm39) |
D252G |
unknown |
Het |
Atxn3 |
A |
G |
12: 101,900,627 (GRCm39) |
S219P |
probably benign |
Het |
Birc6 |
T |
C |
17: 74,954,383 (GRCm39) |
S3397P |
probably damaging |
Het |
Bivm |
A |
G |
1: 44,182,033 (GRCm39) |
I414V |
possibly damaging |
Het |
Cemip |
A |
G |
7: 83,584,945 (GRCm39) |
F1324L |
possibly damaging |
Het |
Ckap5 |
T |
A |
2: 91,445,616 (GRCm39) |
N1724K |
probably damaging |
Het |
Corin |
T |
A |
5: 72,460,178 (GRCm39) |
M1035L |
probably damaging |
Het |
Ctnna3 |
T |
C |
10: 64,709,094 (GRCm39) |
I711T |
probably damaging |
Het |
Cts6 |
A |
T |
13: 61,349,415 (GRCm39) |
W98R |
probably null |
Het |
Dip2a |
A |
G |
10: 76,130,367 (GRCm39) |
S580P |
probably damaging |
Het |
Dock6 |
A |
G |
9: 21,723,068 (GRCm39) |
|
probably null |
Het |
Dusp15 |
T |
A |
2: 152,791,002 (GRCm39) |
T32S |
probably damaging |
Het |
Eogt |
T |
A |
6: 97,093,016 (GRCm39) |
N387I |
probably damaging |
Het |
Evx2 |
T |
C |
2: 74,489,675 (GRCm39) |
D29G |
probably benign |
Het |
Fat1 |
A |
G |
8: 45,466,007 (GRCm39) |
N1422S |
probably benign |
Het |
Fat2 |
T |
C |
11: 55,201,463 (GRCm39) |
D537G |
probably damaging |
Het |
Fat3 |
A |
C |
9: 16,289,244 (GRCm39) |
I93S |
probably benign |
Het |
Fem1b |
T |
C |
9: 62,704,576 (GRCm39) |
E228G |
probably damaging |
Het |
Fh1 |
A |
G |
1: 175,448,072 (GRCm39) |
T25A |
probably benign |
Het |
Fndc3b |
A |
G |
3: 27,514,097 (GRCm39) |
W695R |
probably damaging |
Het |
Gaa |
G |
A |
11: 119,163,813 (GRCm39) |
V222I |
possibly damaging |
Het |
Ggnbp1 |
T |
C |
17: 27,251,947 (GRCm39) |
|
probably null |
Het |
Gipc1 |
A |
G |
8: 84,388,756 (GRCm39) |
Y154C |
probably benign |
Het |
Gm5356 |
G |
T |
8: 89,913,670 (GRCm39) |
|
noncoding transcript |
Het |
Gnl1 |
T |
A |
17: 36,298,603 (GRCm39) |
|
probably null |
Het |
Gpcpd1 |
C |
T |
2: 132,376,019 (GRCm39) |
G605R |
probably damaging |
Het |
Guca1a |
T |
C |
17: 47,705,662 (GRCm39) |
T177A |
possibly damaging |
Het |
Ifit1bl1 |
T |
C |
19: 34,572,076 (GRCm39) |
E127G |
probably damaging |
Het |
Ift81 |
A |
T |
5: 122,729,282 (GRCm39) |
I350N |
probably damaging |
Het |
Ikbke |
GCC |
G |
1: 131,203,004 (GRCm39) |
|
probably null |
Het |
Ing4 |
A |
G |
6: 125,020,946 (GRCm39) |
R23G |
probably damaging |
Het |
Ins1 |
A |
G |
19: 52,253,384 (GRCm39) |
N108S |
probably damaging |
Het |
Iqce |
A |
T |
5: 140,679,214 (GRCm39) |
M72K |
possibly damaging |
Het |
Itga3 |
C |
A |
11: 94,967,097 (GRCm39) |
M22I |
probably benign |
Het |
Kctd18 |
T |
C |
1: 58,001,152 (GRCm39) |
E201G |
probably damaging |
Het |
Klc1 |
A |
G |
12: 111,748,129 (GRCm39) |
N344S |
probably damaging |
Het |
Klrb1f |
A |
T |
6: 129,033,347 (GRCm39) |
I192F |
probably damaging |
Het |
Klrg2 |
A |
T |
6: 38,607,214 (GRCm39) |
|
probably null |
Het |
Kntc1 |
A |
C |
5: 123,897,128 (GRCm39) |
I164L |
probably benign |
Het |
Ltf |
T |
A |
9: 110,855,058 (GRCm39) |
I357K |
probably benign |
Het |
Mr1 |
T |
C |
1: 155,006,436 (GRCm39) |
T304A |
probably benign |
Het |
Msh6 |
C |
T |
17: 88,290,947 (GRCm39) |
R178C |
possibly damaging |
Het |
Mtch1 |
T |
C |
17: 29,566,565 (GRCm39) |
D66G |
probably benign |
Het |
Mtmr7 |
A |
G |
8: 41,062,040 (GRCm39) |
V15A |
probably benign |
Het |
Mtss2 |
A |
T |
8: 111,452,875 (GRCm39) |
H40L |
possibly damaging |
Het |
Mxra8 |
A |
G |
4: 155,925,331 (GRCm39) |
|
probably benign |
Het |
Myo3b |
T |
C |
2: 70,075,253 (GRCm39) |
L535P |
probably damaging |
Het |
Neurl2 |
T |
A |
2: 164,674,739 (GRCm39) |
|
probably null |
Het |
Nfia |
A |
C |
4: 97,970,048 (GRCm39) |
T503P |
probably damaging |
Het |
Noa1 |
T |
C |
5: 77,454,179 (GRCm39) |
E487G |
possibly damaging |
Het |
Nuak1 |
A |
T |
10: 84,211,143 (GRCm39) |
V315D |
probably damaging |
Het |
Nup205 |
A |
G |
6: 35,207,505 (GRCm39) |
N1519S |
possibly damaging |
Het |
Or10x1 |
T |
A |
1: 174,196,966 (GRCm39) |
I161K |
probably damaging |
Het |
Or1l4b |
T |
C |
2: 37,036,266 (GRCm39) |
L14P |
probably damaging |
Het |
Or1o1 |
T |
C |
17: 37,716,589 (GRCm39) |
V50A |
probably benign |
Het |
Or51f1e |
A |
G |
7: 102,747,526 (GRCm39) |
I193V |
possibly damaging |
Het |
Or6b13 |
G |
T |
7: 139,782,340 (GRCm39) |
C114* |
probably null |
Het |
Peli1 |
T |
A |
11: 21,098,528 (GRCm39) |
|
probably benign |
Het |
Ppp6r1 |
A |
G |
7: 4,646,206 (GRCm39) |
L175P |
probably damaging |
Het |
Prkcd |
A |
G |
14: 30,321,700 (GRCm39) |
L498P |
probably damaging |
Het |
Prss30 |
T |
A |
17: 24,191,769 (GRCm39) |
I251F |
probably benign |
Het |
Psme3 |
A |
T |
11: 101,207,907 (GRCm39) |
N21Y |
probably benign |
Het |
Ptpra |
T |
C |
2: 130,374,081 (GRCm39) |
Y271H |
probably damaging |
Het |
Ralgapa1 |
T |
A |
12: 55,745,588 (GRCm39) |
N1303Y |
probably damaging |
Het |
Rims4 |
T |
C |
2: 163,707,463 (GRCm39) |
I121V |
probably benign |
Het |
Rnf123 |
A |
T |
9: 107,933,290 (GRCm39) |
L1149Q |
probably damaging |
Het |
Ryr3 |
T |
A |
2: 112,738,807 (GRCm39) |
L593F |
probably damaging |
Het |
Sec23b |
T |
C |
2: 144,427,519 (GRCm39) |
F582S |
probably damaging |
Het |
Sgpl1 |
T |
C |
10: 60,940,297 (GRCm39) |
K335R |
probably benign |
Het |
Sirpa |
C |
T |
2: 129,451,163 (GRCm39) |
T141I |
probably damaging |
Het |
Slit1 |
G |
T |
19: 41,637,983 (GRCm39) |
A270E |
probably benign |
Het |
Snap91 |
T |
C |
9: 86,674,613 (GRCm39) |
T533A |
possibly damaging |
Het |
Sphkap |
T |
G |
1: 83,255,105 (GRCm39) |
E881D |
probably benign |
Het |
Sptan1 |
C |
A |
2: 29,901,054 (GRCm39) |
R1407S |
probably damaging |
Het |
Tfdp1 |
A |
G |
8: 13,423,895 (GRCm39) |
T353A |
probably benign |
Het |
Ttyh1 |
A |
G |
7: 4,125,533 (GRCm39) |
I62V |
possibly damaging |
Het |
Vwde |
A |
T |
6: 13,196,047 (GRCm39) |
V326D |
possibly damaging |
Het |
Zfp398 |
T |
C |
6: 47,836,446 (GRCm39) |
I82T |
possibly damaging |
Het |
Zp1 |
A |
G |
19: 10,896,198 (GRCm39) |
Y176H |
possibly damaging |
Het |
|
Other mutations in Or9s18 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02684:Or9s18
|
APN |
13 |
65,300,210 (GRCm39) |
missense |
probably damaging |
0.99 |
R0269:Or9s18
|
UTSW |
13 |
65,300,692 (GRCm39) |
missense |
possibly damaging |
0.56 |
R0617:Or9s18
|
UTSW |
13 |
65,300,692 (GRCm39) |
missense |
possibly damaging |
0.56 |
R0646:Or9s18
|
UTSW |
13 |
65,300,877 (GRCm39) |
missense |
probably damaging |
1.00 |
R1338:Or9s18
|
UTSW |
13 |
65,300,197 (GRCm39) |
missense |
probably damaging |
1.00 |
R1893:Or9s18
|
UTSW |
13 |
65,300,806 (GRCm39) |
missense |
possibly damaging |
0.92 |
R3108:Or9s18
|
UTSW |
13 |
65,300,875 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4408:Or9s18
|
UTSW |
13 |
65,300,514 (GRCm39) |
missense |
probably benign |
0.00 |
R4625:Or9s18
|
UTSW |
13 |
65,300,674 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4732:Or9s18
|
UTSW |
13 |
65,300,467 (GRCm39) |
missense |
possibly damaging |
0.72 |
R4733:Or9s18
|
UTSW |
13 |
65,300,467 (GRCm39) |
missense |
possibly damaging |
0.72 |
R5058:Or9s18
|
UTSW |
13 |
65,300,743 (GRCm39) |
missense |
possibly damaging |
0.96 |
R5419:Or9s18
|
UTSW |
13 |
65,300,588 (GRCm39) |
missense |
probably damaging |
1.00 |
R5569:Or9s18
|
UTSW |
13 |
65,300,793 (GRCm39) |
missense |
possibly damaging |
0.81 |
R5662:Or9s18
|
UTSW |
13 |
65,300,067 (GRCm39) |
missense |
possibly damaging |
0.76 |
R7292:Or9s18
|
UTSW |
13 |
65,300,656 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7345:Or9s18
|
UTSW |
13 |
65,300,557 (GRCm39) |
missense |
possibly damaging |
0.59 |
R7427:Or9s18
|
UTSW |
13 |
65,300,866 (GRCm39) |
missense |
probably damaging |
1.00 |
R7428:Or9s18
|
UTSW |
13 |
65,300,866 (GRCm39) |
missense |
probably damaging |
1.00 |
R8162:Or9s18
|
UTSW |
13 |
65,300,734 (GRCm39) |
missense |
probably damaging |
0.99 |
R8736:Or9s18
|
UTSW |
13 |
65,300,538 (GRCm39) |
missense |
probably damaging |
1.00 |
R9224:Or9s18
|
UTSW |
13 |
65,300,203 (GRCm39) |
missense |
probably damaging |
1.00 |
R9607:Or9s18
|
UTSW |
13 |
65,300,885 (GRCm39) |
missense |
probably benign |
0.33 |
R9739:Or9s18
|
UTSW |
13 |
65,300,442 (GRCm39) |
missense |
probably damaging |
1.00 |
|