Other mutations in this stock |
Total: 63 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acad11 |
T |
C |
9: 103,950,822 (GRCm39) |
S49P |
probably damaging |
Het |
Afm |
T |
C |
5: 90,674,238 (GRCm39) |
I250T |
possibly damaging |
Het |
Alox5 |
G |
A |
6: 116,400,106 (GRCm39) |
Q278* |
probably null |
Het |
Anxa7 |
G |
A |
14: 20,512,775 (GRCm39) |
R253C |
probably damaging |
Het |
Arfgef1 |
T |
A |
1: 10,243,164 (GRCm39) |
T1059S |
probably damaging |
Het |
Arpp21 |
T |
C |
9: 112,008,197 (GRCm39) |
E101G |
probably damaging |
Het |
Bcr |
A |
T |
10: 74,897,338 (GRCm39) |
I161F |
possibly damaging |
Het |
Ccdc141 |
T |
C |
2: 76,845,140 (GRCm39) |
E1309G |
probably damaging |
Het |
Ccdc39 |
T |
C |
3: 33,880,629 (GRCm39) |
K446R |
probably damaging |
Het |
Cep41 |
C |
T |
6: 30,657,356 (GRCm39) |
S233N |
probably damaging |
Het |
Col5a1 |
T |
G |
2: 27,812,076 (GRCm39) |
S53A |
unknown |
Het |
Cplane1 |
C |
T |
15: 8,276,422 (GRCm39) |
Q2689* |
probably null |
Het |
Efnb2 |
A |
G |
8: 8,672,329 (GRCm39) |
|
probably null |
Het |
Epb41l5 |
T |
C |
1: 119,477,606 (GRCm39) |
|
probably benign |
Het |
Eri2 |
A |
G |
7: 119,390,397 (GRCm39) |
F77S |
probably damaging |
Het |
Ern1 |
C |
T |
11: 106,312,806 (GRCm39) |
|
probably benign |
Het |
Eya3 |
T |
C |
4: 132,434,440 (GRCm39) |
|
probably benign |
Het |
Icos |
T |
C |
1: 61,033,802 (GRCm39) |
L144P |
probably damaging |
Het |
Ipo8 |
A |
G |
6: 148,690,591 (GRCm39) |
V717A |
probably benign |
Het |
Lrp12 |
T |
C |
15: 39,742,019 (GRCm39) |
E232G |
probably damaging |
Het |
Lrp1b |
A |
G |
2: 40,888,228 (GRCm39) |
I2344T |
probably damaging |
Het |
Mettl5 |
A |
T |
2: 69,701,633 (GRCm39) |
F207I |
possibly damaging |
Het |
Mtor |
G |
T |
4: 148,575,871 (GRCm39) |
E1342* |
probably null |
Het |
Nrap |
A |
G |
19: 56,315,725 (GRCm39) |
Y1360H |
possibly damaging |
Het |
Nsun7 |
T |
C |
5: 66,418,423 (GRCm39) |
V51A |
probably damaging |
Het |
Or5an11 |
C |
A |
19: 12,246,258 (GRCm39) |
F221L |
probably benign |
Het |
Or5p5 |
T |
C |
7: 107,414,469 (GRCm39) |
L228P |
probably damaging |
Het |
Or8k27 |
T |
C |
2: 86,275,664 (GRCm39) |
I221V |
probably benign |
Het |
Or9m1b |
T |
A |
2: 87,836,915 (GRCm39) |
Y60F |
probably damaging |
Het |
Otud6b |
A |
C |
4: 14,818,473 (GRCm39) |
L143V |
probably damaging |
Het |
Pabir2 |
T |
C |
X: 52,335,023 (GRCm39) |
*256W |
probably null |
Het |
Pp2d1 |
T |
C |
17: 53,822,835 (GRCm39) |
N77S |
probably benign |
Het |
Ppp4r3c2 |
A |
T |
X: 88,797,283 (GRCm39) |
M372L |
probably benign |
Het |
Ptpro |
T |
A |
6: 137,420,592 (GRCm39) |
V1007D |
probably damaging |
Het |
Pwwp4a |
G |
T |
X: 72,171,261 (GRCm39) |
G218C |
probably damaging |
Het |
Raly |
G |
T |
2: 154,699,273 (GRCm39) |
G26* |
probably null |
Het |
Rarb |
T |
C |
14: 16,435,177 (GRCm38) |
M290V |
possibly damaging |
Het |
Rusc2 |
A |
G |
4: 43,421,617 (GRCm39) |
E679G |
possibly damaging |
Het |
Scap |
T |
C |
9: 110,213,841 (GRCm39) |
V1268A |
probably damaging |
Het |
Setd1b |
C |
T |
5: 123,298,748 (GRCm39) |
|
probably benign |
Het |
Shisa3 |
C |
G |
5: 67,768,777 (GRCm39) |
P226A |
probably benign |
Het |
Smox |
C |
T |
2: 131,364,051 (GRCm39) |
S481F |
probably damaging |
Het |
Stard9 |
T |
C |
2: 120,531,453 (GRCm39) |
V2570A |
probably benign |
Het |
Sucla2 |
C |
T |
14: 73,798,074 (GRCm39) |
|
probably benign |
Het |
Sult4a1 |
C |
T |
15: 83,970,847 (GRCm39) |
R186Q |
probably benign |
Het |
Taf2 |
G |
T |
15: 54,901,806 (GRCm39) |
A796E |
possibly damaging |
Het |
Taf4b |
T |
C |
18: 14,954,484 (GRCm39) |
|
probably benign |
Het |
Thbs4 |
G |
T |
13: 92,898,041 (GRCm39) |
Q593K |
probably benign |
Het |
Tigd3 |
T |
C |
19: 5,941,753 (GRCm39) |
D459G |
probably benign |
Het |
Tmem168 |
A |
T |
6: 13,591,400 (GRCm39) |
L472Q |
probably damaging |
Het |
Tmem169 |
G |
T |
1: 72,339,875 (GRCm39) |
V102F |
probably damaging |
Het |
Tmem241 |
T |
C |
18: 12,126,631 (GRCm39) |
T274A |
probably benign |
Het |
Trip10 |
A |
G |
17: 57,557,800 (GRCm39) |
Y28C |
probably damaging |
Het |
Ubp1 |
T |
C |
9: 113,799,239 (GRCm39) |
V398A |
probably benign |
Het |
Ubr3 |
A |
G |
2: 69,775,415 (GRCm39) |
Y567C |
probably damaging |
Het |
Uckl1 |
A |
T |
2: 181,211,362 (GRCm39) |
M489K |
possibly damaging |
Het |
Ush2a |
C |
T |
1: 188,169,080 (GRCm39) |
P1074S |
probably damaging |
Het |
Vmn1r62 |
T |
C |
7: 5,678,904 (GRCm39) |
V195A |
probably damaging |
Het |
Vmn2r63 |
T |
A |
7: 42,577,339 (GRCm39) |
I400L |
probably benign |
Het |
Vmn2r67 |
T |
A |
7: 84,800,824 (GRCm39) |
I371F |
probably benign |
Het |
Wdr64 |
A |
G |
1: 175,633,568 (GRCm39) |
T940A |
probably benign |
Het |
Zfp105 |
A |
T |
9: 122,759,742 (GRCm39) |
Y471F |
probably damaging |
Het |
Zfp287 |
A |
T |
11: 62,605,166 (GRCm39) |
H580Q |
probably damaging |
Het |
|
Other mutations in Or8g18 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00981:Or8g18
|
APN |
9 |
39,148,901 (GRCm39) |
missense |
probably benign |
0.25 |
IGL01691:Or8g18
|
APN |
9 |
39,149,315 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02606:Or8g18
|
APN |
9 |
39,149,490 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02656:Or8g18
|
APN |
9 |
39,149,456 (GRCm39) |
missense |
probably benign |
0.13 |
R0133:Or8g18
|
UTSW |
9 |
39,149,307 (GRCm39) |
missense |
probably benign |
0.00 |
R0548:Or8g18
|
UTSW |
9 |
39,149,667 (GRCm39) |
missense |
probably benign |
0.13 |
R0558:Or8g18
|
UTSW |
9 |
39,149,496 (GRCm39) |
missense |
probably damaging |
0.96 |
R0616:Or8g18
|
UTSW |
9 |
39,148,946 (GRCm39) |
missense |
probably benign |
0.00 |
R0626:Or8g18
|
UTSW |
9 |
39,149,162 (GRCm39) |
missense |
possibly damaging |
0.52 |
R0826:Or8g18
|
UTSW |
9 |
39,149,725 (GRCm39) |
start codon destroyed |
probably null |
0.00 |
R0839:Or8g18
|
UTSW |
9 |
39,149,146 (GRCm39) |
missense |
possibly damaging |
0.51 |
R1074:Or8g18
|
UTSW |
9 |
39,149,547 (GRCm39) |
missense |
probably benign |
0.39 |
R1224:Or8g18
|
UTSW |
9 |
39,149,547 (GRCm39) |
missense |
probably benign |
0.39 |
R1226:Or8g18
|
UTSW |
9 |
39,149,547 (GRCm39) |
missense |
probably benign |
0.39 |
R1252:Or8g18
|
UTSW |
9 |
39,149,547 (GRCm39) |
missense |
probably benign |
0.39 |
R1256:Or8g18
|
UTSW |
9 |
39,149,547 (GRCm39) |
missense |
probably benign |
0.39 |
R1355:Or8g18
|
UTSW |
9 |
39,149,547 (GRCm39) |
missense |
probably benign |
0.39 |
R1356:Or8g18
|
UTSW |
9 |
39,149,547 (GRCm39) |
missense |
probably benign |
0.39 |
R1499:Or8g18
|
UTSW |
9 |
39,149,547 (GRCm39) |
missense |
probably benign |
0.39 |
R1658:Or8g18
|
UTSW |
9 |
39,149,255 (GRCm39) |
missense |
probably benign |
0.03 |
R1815:Or8g18
|
UTSW |
9 |
39,149,286 (GRCm39) |
missense |
probably benign |
0.01 |
R2198:Or8g18
|
UTSW |
9 |
39,149,048 (GRCm39) |
missense |
possibly damaging |
0.48 |
R4178:Or8g18
|
UTSW |
9 |
39,149,375 (GRCm39) |
nonsense |
probably null |
|
R5112:Or8g18
|
UTSW |
9 |
39,149,717 (GRCm39) |
start codon destroyed |
probably null |
0.94 |
R6251:Or8g18
|
UTSW |
9 |
39,149,514 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6850:Or8g18
|
UTSW |
9 |
39,149,271 (GRCm39) |
missense |
probably benign |
0.01 |
R7032:Or8g18
|
UTSW |
9 |
39,148,983 (GRCm39) |
missense |
possibly damaging |
0.73 |
R7573:Or8g18
|
UTSW |
9 |
39,148,977 (GRCm39) |
missense |
probably benign |
0.42 |
R7715:Or8g18
|
UTSW |
9 |
39,149,174 (GRCm39) |
missense |
probably damaging |
1.00 |
R7722:Or8g18
|
UTSW |
9 |
39,148,885 (GRCm39) |
nonsense |
probably null |
|
R7729:Or8g18
|
UTSW |
9 |
39,149,546 (GRCm39) |
missense |
probably benign |
0.28 |
R8710:Or8g18
|
UTSW |
9 |
39,149,306 (GRCm39) |
missense |
probably benign |
0.00 |
R9513:Or8g18
|
UTSW |
9 |
39,149,625 (GRCm39) |
missense |
probably benign |
0.05 |
R9515:Or8g18
|
UTSW |
9 |
39,149,625 (GRCm39) |
missense |
probably benign |
0.05 |
|