Other mutations in this stock |
Total: 41 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca2 |
C |
T |
2: 25,323,968 (GRCm39) |
|
probably benign |
Het |
Bloc1s2-ps |
C |
T |
2: 52,509,914 (GRCm39) |
A50V |
probably benign |
Het |
Bltp3b |
T |
C |
10: 89,627,240 (GRCm39) |
L435P |
probably benign |
Het |
Col4a3 |
A |
G |
1: 82,647,441 (GRCm39) |
D455G |
unknown |
Het |
Col4a3 |
A |
G |
1: 82,647,976 (GRCm39) |
I496V |
unknown |
Het |
Coro1c |
A |
T |
5: 113,987,675 (GRCm39) |
M222K |
probably benign |
Het |
Dnah5 |
T |
A |
15: 28,410,149 (GRCm39) |
|
probably null |
Het |
Emc4 |
C |
A |
2: 112,197,871 (GRCm39) |
|
probably benign |
Het |
Fcer2a |
T |
C |
8: 3,738,842 (GRCm39) |
D32G |
possibly damaging |
Het |
Fhip1a |
A |
G |
3: 85,572,808 (GRCm39) |
|
probably benign |
Het |
Garnl3 |
T |
C |
2: 32,896,828 (GRCm39) |
K559E |
probably damaging |
Het |
Gckr |
T |
C |
5: 31,466,381 (GRCm39) |
L452P |
probably damaging |
Het |
Gm4841 |
A |
G |
18: 60,403,124 (GRCm39) |
V323A |
probably damaging |
Het |
Gm6902 |
T |
A |
7: 22,973,087 (GRCm39) |
I147L |
probably benign |
Het |
Gpr75 |
T |
C |
11: 30,841,755 (GRCm39) |
V220A |
probably benign |
Het |
Hdac6 |
A |
G |
X: 7,813,237 (GRCm39) |
S42P |
probably benign |
Het |
Hdhd2 |
A |
G |
18: 77,044,607 (GRCm39) |
N128S |
probably damaging |
Het |
Hsd3b2 |
G |
T |
3: 98,618,995 (GRCm39) |
R317S |
probably damaging |
Het |
Il23r |
T |
A |
6: 67,400,909 (GRCm39) |
I474F |
probably damaging |
Het |
Itga5 |
T |
C |
15: 103,255,102 (GRCm39) |
Y954C |
probably benign |
Het |
Itgam |
T |
C |
7: 127,679,445 (GRCm39) |
F196L |
possibly damaging |
Het |
Mapkbp1 |
T |
C |
2: 119,852,339 (GRCm39) |
V957A |
possibly damaging |
Het |
Mblac2 |
T |
C |
13: 81,898,125 (GRCm39) |
M167T |
probably damaging |
Het |
Mterf4 |
C |
T |
1: 93,232,812 (GRCm39) |
R13H |
possibly damaging |
Het |
Or5h18 |
G |
A |
16: 58,848,192 (GRCm39) |
P26L |
probably benign |
Het |
Or6c76b |
A |
G |
10: 129,692,497 (GRCm39) |
I37V |
probably benign |
Het |
Phldb2 |
A |
G |
16: 45,645,423 (GRCm39) |
L386P |
probably damaging |
Het |
Ppp1r13b |
A |
G |
12: 111,799,653 (GRCm39) |
I708T |
probably benign |
Het |
Pramel31 |
A |
G |
4: 144,090,195 (GRCm39) |
I412V |
probably benign |
Het |
Ramp2 |
T |
A |
11: 101,138,453 (GRCm39) |
Y85N |
probably benign |
Het |
Rnf217 |
A |
G |
10: 31,484,499 (GRCm39) |
Y228H |
probably damaging |
Het |
Rock1 |
T |
G |
18: 10,080,502 (GRCm39) |
D1014A |
probably benign |
Het |
Scyl3 |
T |
A |
1: 163,762,338 (GRCm39) |
C101* |
probably null |
Het |
Sema6b |
G |
T |
17: 56,439,761 (GRCm39) |
L27I |
possibly damaging |
Het |
Slc10a5 |
A |
G |
3: 10,400,369 (GRCm39) |
V97A |
probably benign |
Het |
Strc |
C |
A |
2: 121,195,541 (GRCm39) |
R1636L |
probably benign |
Het |
Tm9sf1 |
T |
A |
14: 55,880,224 (GRCm39) |
T58S |
probably damaging |
Het |
Tmem106c |
T |
C |
15: 97,864,825 (GRCm39) |
Y85H |
probably damaging |
Het |
Vmn2r9 |
A |
G |
5: 108,990,811 (GRCm39) |
|
probably null |
Het |
Vps13a |
A |
G |
19: 16,628,781 (GRCm39) |
|
probably null |
Het |
Zfp976 |
A |
T |
7: 42,263,333 (GRCm39) |
L168* |
probably null |
Het |
|
Other mutations in Npffr1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02971:Npffr1
|
APN |
10 |
61,449,918 (GRCm39) |
missense |
probably damaging |
1.00 |
R0893:Npffr1
|
UTSW |
10 |
61,450,010 (GRCm39) |
missense |
possibly damaging |
0.88 |
R1528:Npffr1
|
UTSW |
10 |
61,450,016 (GRCm39) |
missense |
possibly damaging |
0.66 |
R1568:Npffr1
|
UTSW |
10 |
61,462,012 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7567:Npffr1
|
UTSW |
10 |
61,462,088 (GRCm39) |
missense |
probably benign |
0.31 |
R7857:Npffr1
|
UTSW |
10 |
61,449,765 (GRCm39) |
missense |
probably benign |
0.01 |
R8111:Npffr1
|
UTSW |
10 |
61,459,128 (GRCm39) |
missense |
probably damaging |
0.99 |
R8113:Npffr1
|
UTSW |
10 |
61,449,750 (GRCm39) |
missense |
possibly damaging |
0.79 |
R8872:Npffr1
|
UTSW |
10 |
61,461,794 (GRCm39) |
missense |
probably benign |
0.00 |
R8889:Npffr1
|
UTSW |
10 |
61,449,939 (GRCm39) |
missense |
possibly damaging |
0.66 |
R8892:Npffr1
|
UTSW |
10 |
61,449,939 (GRCm39) |
missense |
possibly damaging |
0.66 |
X0024:Npffr1
|
UTSW |
10 |
61,461,841 (GRCm39) |
missense |
possibly damaging |
0.91 |
|