Other mutations in this stock |
Total: 58 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930486L24Rik |
A |
G |
13: 60,993,041 (GRCm39) |
Y213H |
probably damaging |
Het |
Alg8 |
C |
T |
7: 97,037,752 (GRCm39) |
H379Y |
probably damaging |
Het |
Arhgef25 |
T |
C |
10: 127,025,605 (GRCm39) |
T12A |
probably benign |
Het |
Arid4a |
A |
G |
12: 71,122,559 (GRCm39) |
E980G |
possibly damaging |
Het |
Aspm |
C |
T |
1: 139,405,792 (GRCm39) |
H1560Y |
probably benign |
Het |
Atg10 |
A |
T |
13: 91,085,499 (GRCm39) |
I150K |
probably damaging |
Het |
Bud13 |
A |
C |
9: 46,201,490 (GRCm39) |
Q387P |
possibly damaging |
Het |
Champ1 |
A |
G |
8: 13,929,939 (GRCm39) |
Y699C |
probably damaging |
Het |
Clstn1 |
A |
G |
4: 149,722,790 (GRCm39) |
E476G |
probably damaging |
Het |
Col2a1 |
T |
C |
15: 97,886,857 (GRCm39) |
D345G |
unknown |
Het |
Col2a1 |
A |
T |
15: 97,898,462 (GRCm39) |
|
probably benign |
Het |
Col9a2 |
C |
G |
4: 120,911,455 (GRCm39) |
R599G |
probably damaging |
Het |
Dnajb2 |
G |
A |
1: 75,218,124 (GRCm39) |
|
probably null |
Het |
Dock4 |
G |
T |
12: 40,844,623 (GRCm39) |
|
probably null |
Het |
Epx |
A |
T |
11: 87,765,656 (GRCm39) |
L101Q |
probably damaging |
Het |
F13a1 |
A |
T |
13: 37,231,398 (GRCm39) |
N21K |
probably damaging |
Het |
Fam13c |
C |
T |
10: 70,378,478 (GRCm39) |
S336L |
probably damaging |
Het |
Foxj3 |
T |
A |
4: 119,473,821 (GRCm39) |
H215Q |
possibly damaging |
Het |
Gcnt4 |
A |
T |
13: 97,083,522 (GRCm39) |
R273* |
probably null |
Het |
Gpam |
T |
C |
19: 55,068,890 (GRCm39) |
N450S |
probably benign |
Het |
Hivep2 |
C |
A |
10: 14,004,713 (GRCm39) |
T437K |
probably benign |
Het |
Hmcn2 |
T |
C |
2: 31,303,419 (GRCm39) |
L3020P |
probably damaging |
Het |
Hmgcr |
A |
G |
13: 96,795,597 (GRCm39) |
I324T |
probably benign |
Het |
Ighmbp2 |
T |
C |
19: 3,321,658 (GRCm39) |
Y367C |
probably benign |
Het |
Lsamp |
A |
T |
16: 41,954,675 (GRCm39) |
E174V |
possibly damaging |
Het |
Mid1ip1 |
T |
C |
X: 10,584,620 (GRCm39) |
V51A |
possibly damaging |
Het |
Mrc2 |
G |
A |
11: 105,239,257 (GRCm39) |
|
probably null |
Het |
Msn |
C |
A |
X: 95,203,805 (GRCm39) |
Q303K |
probably damaging |
Het |
Myh7b |
A |
G |
2: 155,474,909 (GRCm39) |
K1816E |
probably damaging |
Het |
Nap1l1 |
T |
A |
10: 111,331,183 (GRCm39) |
|
probably null |
Het |
Nme2 |
T |
A |
11: 93,840,803 (GRCm39) |
E252D |
probably benign |
Het |
Ntpcr |
G |
A |
8: 126,464,111 (GRCm39) |
V79M |
probably damaging |
Het |
Ogdh |
C |
T |
11: 6,288,627 (GRCm39) |
R235* |
probably null |
Het |
Or10d1 |
A |
G |
9: 39,484,267 (GRCm39) |
V96A |
probably benign |
Het |
Or10w1 |
A |
G |
19: 13,632,321 (GRCm39) |
D176G |
probably benign |
Het |
Or9k2 |
C |
A |
10: 129,998,275 (GRCm39) |
E307* |
probably null |
Het |
P3r3urf |
A |
G |
4: 116,030,718 (GRCm39) |
T41A |
probably benign |
Het |
Pcdh20 |
T |
C |
14: 88,705,899 (GRCm39) |
N467S |
probably benign |
Het |
Pkhd1 |
G |
A |
1: 20,604,853 (GRCm39) |
T1154I |
possibly damaging |
Het |
Polq |
G |
T |
16: 36,898,711 (GRCm39) |
R2157I |
probably damaging |
Het |
Reep6 |
C |
A |
10: 80,171,723 (GRCm39) |
A533E |
probably damaging |
Het |
Senp2 |
T |
C |
16: 21,828,485 (GRCm39) |
S32P |
probably damaging |
Het |
Septin11 |
T |
A |
5: 93,296,258 (GRCm39) |
I52N |
probably damaging |
Het |
Shld2 |
T |
C |
14: 33,967,325 (GRCm39) |
D77G |
probably benign |
Het |
Slc17a4 |
C |
T |
13: 24,085,752 (GRCm39) |
R387H |
probably benign |
Het |
Spdye4b |
C |
T |
5: 143,178,084 (GRCm39) |
T11I |
probably benign |
Het |
Srrt |
C |
T |
5: 137,300,387 (GRCm39) |
|
probably null |
Het |
Sspo |
T |
A |
6: 48,457,754 (GRCm39) |
C3085S |
probably damaging |
Het |
Stim1 |
C |
T |
7: 102,060,503 (GRCm39) |
T182I |
possibly damaging |
Het |
Thbs2 |
C |
A |
17: 14,908,113 (GRCm39) |
V217L |
probably benign |
Het |
Thpo |
G |
A |
16: 20,547,498 (GRCm39) |
R38C |
probably damaging |
Het |
Tmem210 |
A |
G |
2: 25,178,444 (GRCm39) |
E35G |
possibly damaging |
Het |
Trim12c |
T |
A |
7: 103,990,075 (GRCm39) |
|
probably benign |
Het |
Tvp23b |
A |
G |
11: 62,774,455 (GRCm39) |
H33R |
possibly damaging |
Het |
Usp14 |
A |
G |
18: 10,024,532 (GRCm39) |
|
probably null |
Het |
Vmn2r73 |
A |
G |
7: 85,507,258 (GRCm39) |
W685R |
probably benign |
Het |
Zfp618 |
G |
A |
4: 63,051,801 (GRCm39) |
A861T |
probably benign |
Het |
Zfp715 |
A |
G |
7: 42,949,180 (GRCm39) |
V260A |
probably benign |
Het |
|
Other mutations in Lrrc14b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00516:Lrrc14b
|
APN |
13 |
74,509,078 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL01521:Lrrc14b
|
APN |
13 |
74,511,691 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03156:Lrrc14b
|
APN |
13 |
74,512,023 (GRCm39) |
missense |
probably benign |
|
R0457:Lrrc14b
|
UTSW |
13 |
74,509,279 (GRCm39) |
missense |
probably benign |
0.41 |
R1631:Lrrc14b
|
UTSW |
13 |
74,509,373 (GRCm39) |
splice site |
probably null |
|
R1741:Lrrc14b
|
UTSW |
13 |
74,511,705 (GRCm39) |
missense |
probably damaging |
1.00 |
R2042:Lrrc14b
|
UTSW |
13 |
74,511,561 (GRCm39) |
missense |
probably benign |
0.00 |
R2047:Lrrc14b
|
UTSW |
13 |
74,511,561 (GRCm39) |
missense |
probably benign |
0.00 |
R2149:Lrrc14b
|
UTSW |
13 |
74,511,876 (GRCm39) |
missense |
possibly damaging |
0.63 |
R3083:Lrrc14b
|
UTSW |
13 |
74,511,337 (GRCm39) |
missense |
possibly damaging |
0.63 |
R3892:Lrrc14b
|
UTSW |
13 |
74,511,787 (GRCm39) |
missense |
probably benign |
0.00 |
R5748:Lrrc14b
|
UTSW |
13 |
74,511,759 (GRCm39) |
missense |
probably damaging |
1.00 |
R6508:Lrrc14b
|
UTSW |
13 |
74,511,337 (GRCm39) |
missense |
possibly damaging |
0.63 |
R6663:Lrrc14b
|
UTSW |
13 |
74,509,480 (GRCm39) |
missense |
probably damaging |
1.00 |
R6687:Lrrc14b
|
UTSW |
13 |
74,508,881 (GRCm39) |
missense |
probably benign |
0.00 |
R7309:Lrrc14b
|
UTSW |
13 |
74,511,321 (GRCm39) |
missense |
probably benign |
0.08 |
R7472:Lrrc14b
|
UTSW |
13 |
74,511,226 (GRCm39) |
missense |
probably damaging |
1.00 |
R7574:Lrrc14b
|
UTSW |
13 |
74,508,892 (GRCm39) |
missense |
probably damaging |
0.98 |
R7629:Lrrc14b
|
UTSW |
13 |
74,509,283 (GRCm39) |
missense |
probably benign |
0.03 |
R7695:Lrrc14b
|
UTSW |
13 |
74,511,297 (GRCm39) |
missense |
possibly damaging |
0.91 |
R8169:Lrrc14b
|
UTSW |
13 |
74,511,286 (GRCm39) |
missense |
possibly damaging |
0.56 |
R8824:Lrrc14b
|
UTSW |
13 |
74,512,068 (GRCm39) |
missense |
probably damaging |
1.00 |
R8852:Lrrc14b
|
UTSW |
13 |
74,509,408 (GRCm39) |
missense |
probably damaging |
1.00 |
R8860:Lrrc14b
|
UTSW |
13 |
74,509,408 (GRCm39) |
missense |
probably damaging |
1.00 |
R9010:Lrrc14b
|
UTSW |
13 |
74,509,151 (GRCm39) |
missense |
possibly damaging |
0.48 |
R9548:Lrrc14b
|
UTSW |
13 |
74,511,996 (GRCm39) |
missense |
probably benign |
0.02 |
|