Other mutations in this stock |
Total: 59 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aass |
T |
A |
6: 23,075,199 (GRCm39) |
D816V |
possibly damaging |
Het |
Abca16 |
A |
T |
7: 120,113,928 (GRCm39) |
N933I |
probably benign |
Het |
Acly |
A |
T |
11: 100,368,839 (GRCm39) |
|
probably null |
Het |
Acox1 |
C |
T |
11: 116,074,406 (GRCm39) |
G105D |
possibly damaging |
Het |
Ankrd24 |
A |
G |
10: 81,482,628 (GRCm39) |
E939G |
possibly damaging |
Het |
Bard1 |
T |
A |
1: 71,106,101 (GRCm39) |
|
probably null |
Het |
Brd4 |
G |
T |
17: 32,432,521 (GRCm39) |
N579K |
unknown |
Het |
C1qc |
T |
C |
4: 136,617,592 (GRCm39) |
Y168C |
probably damaging |
Het |
Casp6 |
A |
G |
3: 129,705,858 (GRCm39) |
D175G |
probably damaging |
Het |
Ccdc83 |
A |
T |
7: 89,873,190 (GRCm39) |
Y388* |
probably null |
Het |
Clasrp |
A |
T |
7: 19,318,516 (GRCm39) |
*628R |
probably null |
Het |
Cox4i1 |
A |
G |
8: 121,400,049 (GRCm39) |
I111V |
probably benign |
Het |
Cpvl |
T |
A |
6: 53,903,886 (GRCm39) |
D293V |
probably damaging |
Het |
Epb41l4b |
C |
T |
4: 57,076,913 (GRCm39) |
|
probably null |
Het |
Frem2 |
C |
A |
3: 53,431,103 (GRCm39) |
L2743F |
possibly damaging |
Het |
Frmd4a |
A |
T |
2: 4,606,160 (GRCm39) |
H628L |
probably benign |
Het |
Fyb1 |
A |
G |
15: 6,690,184 (GRCm39) |
D809G |
probably damaging |
Het |
Gm19410 |
T |
A |
8: 36,274,652 (GRCm39) |
M1491K |
possibly damaging |
Het |
Gm3604 |
G |
A |
13: 62,517,810 (GRCm39) |
H183Y |
possibly damaging |
Het |
H1f7 |
A |
G |
15: 98,154,565 (GRCm39) |
S195P |
unknown |
Het |
Lama2 |
T |
C |
10: 26,866,920 (GRCm39) |
Y2858C |
probably damaging |
Het |
Methig1 |
T |
C |
15: 100,251,412 (GRCm39) |
F108L |
probably benign |
Het |
Mfsd4b5 |
A |
G |
10: 39,846,251 (GRCm39) |
V443A |
probably damaging |
Het |
Muc5ac |
G |
C |
7: 141,363,040 (GRCm39) |
G2117A |
unknown |
Het |
Myh9 |
C |
T |
15: 77,667,610 (GRCm39) |
V608I |
probably benign |
Het |
Myo1g |
T |
C |
11: 6,464,849 (GRCm39) |
D475G |
probably damaging |
Het |
Neb |
A |
C |
2: 52,170,728 (GRCm39) |
|
probably null |
Het |
Nlrp1b |
T |
A |
11: 71,059,665 (GRCm39) |
I769F |
probably benign |
Het |
Nol8 |
G |
T |
13: 49,815,742 (GRCm39) |
V617F |
possibly damaging |
Het |
Or2d2b |
A |
T |
7: 106,705,740 (GRCm39) |
C109* |
probably null |
Het |
Pik3r2 |
A |
G |
8: 71,223,545 (GRCm39) |
F346S |
probably damaging |
Het |
Pou3f3 |
T |
A |
1: 42,737,308 (GRCm39) |
F335I |
probably damaging |
Het |
Ppp1r3e |
T |
C |
14: 55,114,084 (GRCm39) |
D196G |
probably damaging |
Het |
Prpf40a |
T |
C |
2: 53,041,757 (GRCm39) |
T545A |
probably damaging |
Het |
Rictor |
C |
T |
15: 6,801,635 (GRCm39) |
S441L |
probably benign |
Het |
Rprd1a |
T |
A |
18: 24,641,311 (GRCm39) |
K102* |
probably null |
Het |
Sim1 |
A |
G |
10: 50,772,131 (GRCm39) |
T47A |
possibly damaging |
Het |
Slc45a1 |
C |
T |
4: 150,728,498 (GRCm39) |
A102T |
probably damaging |
Het |
Slc6a11 |
C |
T |
6: 114,207,098 (GRCm39) |
P361S |
possibly damaging |
Het |
Slc9b2 |
T |
C |
3: 135,031,998 (GRCm39) |
F286S |
probably damaging |
Het |
Slco4a1 |
T |
C |
2: 180,113,030 (GRCm39) |
S421P |
probably benign |
Het |
Snap91 |
A |
C |
9: 86,680,762 (GRCm39) |
|
probably null |
Het |
Sppl2a |
A |
G |
2: 126,761,625 (GRCm39) |
L293P |
probably damaging |
Het |
Sval3 |
T |
A |
6: 41,949,360 (GRCm39) |
I66K |
possibly damaging |
Het |
Synj2bp |
T |
C |
12: 81,551,311 (GRCm39) |
I85V |
probably benign |
Het |
Thop1 |
G |
T |
10: 80,916,025 (GRCm39) |
A403S |
probably benign |
Het |
Tmco5b |
A |
G |
2: 113,118,609 (GRCm39) |
N111D |
probably damaging |
Het |
Trip10 |
G |
A |
17: 57,568,667 (GRCm39) |
V419I |
possibly damaging |
Het |
Trpv3 |
T |
C |
11: 73,176,847 (GRCm39) |
Y409H |
probably damaging |
Het |
Tulp4 |
A |
G |
17: 6,283,399 (GRCm39) |
T1143A |
probably damaging |
Het |
Ugt2b5 |
A |
T |
5: 87,288,108 (GRCm39) |
S20T |
probably benign |
Het |
Unc5b |
A |
G |
10: 60,610,823 (GRCm39) |
F406L |
probably benign |
Het |
Usf3 |
A |
G |
16: 44,040,884 (GRCm39) |
E1788G |
probably benign |
Het |
Usp45 |
A |
G |
4: 21,780,430 (GRCm39) |
D27G |
probably damaging |
Het |
Vmn2r100 |
G |
A |
17: 19,742,726 (GRCm39) |
V367I |
probably benign |
Het |
Vmn2r49 |
T |
A |
7: 9,710,185 (GRCm39) |
K849I |
probably damaging |
Het |
Zfp119b |
A |
T |
17: 56,245,682 (GRCm39) |
H501Q |
probably damaging |
Het |
Zfp462 |
C |
A |
4: 55,016,958 (GRCm39) |
H893N |
probably benign |
Het |
Zkscan4 |
A |
G |
13: 21,663,525 (GRCm39) |
E88G |
probably damaging |
Het |
|
Other mutations in Timd4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02140:Timd4
|
APN |
11 |
46,710,841 (GRCm39) |
missense |
possibly damaging |
0.61 |
IGL02247:Timd4
|
APN |
11 |
46,706,558 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02803:Timd4
|
APN |
11 |
46,706,521 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02991:Timd4
|
APN |
11 |
46,732,974 (GRCm39) |
splice site |
probably benign |
|
R0318:Timd4
|
UTSW |
11 |
46,727,898 (GRCm39) |
missense |
probably benign |
0.00 |
R0427:Timd4
|
UTSW |
11 |
46,710,084 (GRCm39) |
missense |
probably benign |
0.00 |
R1175:Timd4
|
UTSW |
11 |
46,708,498 (GRCm39) |
missense |
probably damaging |
1.00 |
R1185:Timd4
|
UTSW |
11 |
46,708,475 (GRCm39) |
missense |
probably damaging |
0.99 |
R1185:Timd4
|
UTSW |
11 |
46,708,475 (GRCm39) |
missense |
probably damaging |
0.99 |
R1185:Timd4
|
UTSW |
11 |
46,708,475 (GRCm39) |
missense |
probably damaging |
0.99 |
R1635:Timd4
|
UTSW |
11 |
46,732,989 (GRCm39) |
missense |
possibly damaging |
0.92 |
R2011:Timd4
|
UTSW |
11 |
46,710,857 (GRCm39) |
missense |
possibly damaging |
0.79 |
R2012:Timd4
|
UTSW |
11 |
46,710,857 (GRCm39) |
missense |
possibly damaging |
0.79 |
R4994:Timd4
|
UTSW |
11 |
46,706,344 (GRCm39) |
missense |
probably damaging |
0.99 |
R5511:Timd4
|
UTSW |
11 |
46,710,807 (GRCm39) |
splice site |
probably null |
|
R5739:Timd4
|
UTSW |
11 |
46,708,573 (GRCm39) |
missense |
probably benign |
0.10 |
R5991:Timd4
|
UTSW |
11 |
46,734,030 (GRCm39) |
makesense |
probably null |
|
R6207:Timd4
|
UTSW |
11 |
46,706,353 (GRCm39) |
missense |
probably damaging |
0.98 |
R6863:Timd4
|
UTSW |
11 |
46,706,270 (GRCm39) |
nonsense |
probably null |
|
R7230:Timd4
|
UTSW |
11 |
46,701,691 (GRCm39) |
missense |
probably benign |
0.01 |
R7254:Timd4
|
UTSW |
11 |
46,734,016 (GRCm39) |
missense |
probably benign |
0.04 |
R7466:Timd4
|
UTSW |
11 |
46,708,585 (GRCm39) |
missense |
probably benign |
0.01 |
R8777:Timd4
|
UTSW |
11 |
46,706,309 (GRCm39) |
missense |
possibly damaging |
0.49 |
R8777-TAIL:Timd4
|
UTSW |
11 |
46,706,309 (GRCm39) |
missense |
possibly damaging |
0.49 |
|