Other mutations in this stock |
Total: 55 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadacl4 |
G |
A |
4: 144,349,750 (GRCm39) |
V336I |
probably benign |
Het |
Aadacl4fm4 |
A |
T |
4: 144,397,216 (GRCm39) |
L172* |
probably null |
Het |
Abcg3 |
T |
C |
5: 105,083,860 (GRCm39) |
T637A |
probably benign |
Het |
Ap3d1 |
G |
A |
10: 80,550,156 (GRCm39) |
R692* |
probably null |
Het |
Aqp2 |
C |
T |
15: 99,481,885 (GRCm39) |
H260Y |
probably benign |
Het |
Btbd2 |
C |
A |
10: 80,480,166 (GRCm39) |
R383L |
probably damaging |
Het |
Ccdc196 |
T |
A |
12: 78,244,141 (GRCm39) |
D31E |
probably damaging |
Het |
Ccdc24 |
T |
C |
4: 117,727,123 (GRCm39) |
T196A |
probably benign |
Het |
Cdc20b |
G |
A |
13: 113,220,509 (GRCm39) |
G463S |
probably damaging |
Het |
Ceacam5 |
A |
T |
7: 17,486,212 (GRCm39) |
R570* |
probably null |
Het |
Col12a1 |
A |
T |
9: 79,584,516 (GRCm39) |
N1357K |
probably damaging |
Het |
Cpa5 |
A |
T |
6: 30,614,053 (GRCm39) |
Q65L |
probably benign |
Het |
Ddo |
A |
C |
10: 40,513,414 (GRCm39) |
M119L |
possibly damaging |
Het |
Dnah8 |
G |
T |
17: 30,981,653 (GRCm39) |
L3058F |
probably damaging |
Het |
Dnajb8 |
A |
G |
6: 88,200,022 (GRCm39) |
N186S |
probably damaging |
Het |
Dock4 |
T |
C |
12: 40,862,325 (GRCm39) |
|
probably null |
Het |
Ear6 |
A |
G |
14: 52,091,885 (GRCm39) |
Y144C |
probably damaging |
Het |
Eng |
T |
A |
2: 32,563,287 (GRCm39) |
I281N |
probably damaging |
Het |
Fgf2 |
A |
G |
3: 37,458,860 (GRCm39) |
K85E |
probably damaging |
Het |
Fubp1 |
A |
T |
3: 151,931,783 (GRCm39) |
Q37L |
probably benign |
Het |
Gabra2 |
G |
T |
5: 71,251,882 (GRCm39) |
P22T |
probably damaging |
Het |
Gm10401 |
T |
C |
5: 115,236,245 (GRCm39) |
|
probably benign |
Het |
Gsdmc |
T |
C |
15: 63,650,556 (GRCm39) |
D275G |
possibly damaging |
Het |
Iglv3 |
A |
G |
16: 19,060,034 (GRCm39) |
I98T |
probably damaging |
Het |
Lmod1 |
G |
T |
1: 135,292,879 (GRCm39) |
R578L |
probably damaging |
Het |
Mindy2 |
A |
G |
9: 70,524,044 (GRCm39) |
|
probably null |
Het |
Neb |
G |
T |
2: 52,183,657 (GRCm39) |
Q1004K |
probably damaging |
Het |
Nkx2-9 |
T |
G |
12: 56,658,674 (GRCm39) |
N180T |
probably benign |
Het |
Nlrp2 |
C |
T |
7: 5,311,709 (GRCm39) |
R922H |
probably benign |
Het |
Nol4l |
T |
C |
2: 153,325,737 (GRCm39) |
E116G |
probably damaging |
Het |
Or1af1 |
A |
T |
2: 37,109,989 (GRCm39) |
M163L |
possibly damaging |
Het |
Pcdhb20 |
A |
C |
18: 37,639,218 (GRCm39) |
E581D |
probably benign |
Het |
Pidd1 |
G |
T |
7: 141,019,331 (GRCm39) |
T750K |
probably benign |
Het |
Rab44 |
A |
G |
17: 29,358,784 (GRCm39) |
E324G |
probably benign |
Het |
Ramp3 |
T |
C |
11: 6,624,768 (GRCm39) |
C21R |
possibly damaging |
Het |
Rpap1 |
A |
C |
2: 119,605,850 (GRCm39) |
M345R |
probably damaging |
Het |
Serpina3k |
A |
C |
12: 104,310,519 (GRCm39) |
K350Q |
probably benign |
Het |
St13 |
C |
T |
15: 81,250,547 (GRCm39) |
|
probably null |
Het |
Stard9 |
A |
T |
2: 120,544,549 (GRCm39) |
K4497* |
probably null |
Het |
Tbx19 |
A |
T |
1: 164,975,202 (GRCm39) |
|
probably null |
Het |
Tgoln1 |
A |
G |
6: 72,592,538 (GRCm39) |
V314A |
possibly damaging |
Het |
Them4 |
A |
T |
3: 94,231,678 (GRCm39) |
I172F |
probably damaging |
Het |
Tmc7 |
T |
A |
7: 118,146,846 (GRCm39) |
Y477F |
probably benign |
Het |
Tmem132a |
A |
G |
19: 10,840,669 (GRCm39) |
L421P |
probably damaging |
Het |
Trim69 |
A |
G |
2: 121,998,391 (GRCm39) |
E121G |
probably damaging |
Het |
Vmn2r11 |
T |
G |
5: 109,194,976 (GRCm39) |
R783S |
possibly damaging |
Het |
Vmn2r62 |
T |
A |
7: 42,438,412 (GRCm39) |
L141F |
probably benign |
Het |
Zbtb7a |
A |
G |
10: 80,983,905 (GRCm39) |
N449S |
possibly damaging |
Het |
Zfhx3 |
C |
T |
8: 109,527,273 (GRCm39) |
R1057W |
probably damaging |
Het |
Zfp180 |
G |
T |
7: 23,805,306 (GRCm39) |
C575F |
probably damaging |
Het |
Zfp462 |
G |
A |
4: 55,012,326 (GRCm39) |
A1431T |
probably benign |
Het |
Zfp592 |
T |
C |
7: 80,673,576 (GRCm39) |
V180A |
probably benign |
Het |
Zfp605 |
C |
T |
5: 110,275,311 (GRCm39) |
P143L |
probably benign |
Het |
Zfp646 |
T |
C |
7: 127,482,505 (GRCm39) |
S1561P |
probably benign |
Het |
Zfp706 |
T |
C |
15: 37,002,190 (GRCm39) |
T46A |
possibly damaging |
Het |
|
Other mutations in Or5ac19 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01734:Or5ac19
|
APN |
16 |
59,089,213 (GRCm39) |
missense |
probably benign |
0.07 |
IGL01985:Or5ac19
|
APN |
16 |
59,089,442 (GRCm39) |
missense |
probably benign |
|
IGL02618:Or5ac19
|
APN |
16 |
59,089,290 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02830:Or5ac19
|
APN |
16 |
59,089,416 (GRCm39) |
missense |
possibly damaging |
0.94 |
PIT4449001:Or5ac19
|
UTSW |
16 |
59,089,493 (GRCm39) |
missense |
probably damaging |
1.00 |
R0047:Or5ac19
|
UTSW |
16 |
59,089,574 (GRCm39) |
missense |
probably damaging |
1.00 |
R0047:Or5ac19
|
UTSW |
16 |
59,089,574 (GRCm39) |
missense |
probably damaging |
1.00 |
R1035:Or5ac19
|
UTSW |
16 |
59,089,307 (GRCm39) |
missense |
probably damaging |
1.00 |
R1037:Or5ac19
|
UTSW |
16 |
59,089,307 (GRCm39) |
missense |
probably damaging |
1.00 |
R1163:Or5ac19
|
UTSW |
16 |
59,089,518 (GRCm39) |
missense |
probably benign |
0.23 |
R1225:Or5ac19
|
UTSW |
16 |
59,089,587 (GRCm39) |
missense |
probably benign |
|
R1519:Or5ac19
|
UTSW |
16 |
59,089,307 (GRCm39) |
missense |
probably damaging |
1.00 |
R1583:Or5ac19
|
UTSW |
16 |
59,089,394 (GRCm39) |
missense |
probably benign |
0.00 |
R2075:Or5ac19
|
UTSW |
16 |
59,089,274 (GRCm39) |
missense |
possibly damaging |
0.60 |
R4591:Or5ac19
|
UTSW |
16 |
59,089,776 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5547:Or5ac19
|
UTSW |
16 |
59,089,479 (GRCm39) |
missense |
probably benign |
0.35 |
R6132:Or5ac19
|
UTSW |
16 |
59,089,367 (GRCm39) |
missense |
probably damaging |
0.97 |
R6737:Or5ac19
|
UTSW |
16 |
59,089,175 (GRCm39) |
missense |
possibly damaging |
0.60 |
R8001:Or5ac19
|
UTSW |
16 |
59,089,472 (GRCm39) |
missense |
probably benign |
0.01 |
R8525:Or5ac19
|
UTSW |
16 |
59,089,571 (GRCm39) |
missense |
probably benign |
0.07 |
R9003:Or5ac19
|
UTSW |
16 |
59,089,263 (GRCm39) |
missense |
probably benign |
0.05 |
R9260:Or5ac19
|
UTSW |
16 |
59,089,677 (GRCm39) |
missense |
probably damaging |
0.98 |
R9584:Or5ac19
|
UTSW |
16 |
59,089,580 (GRCm39) |
missense |
probably benign |
0.05 |
|