Other mutations in this stock |
Total: 70 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acad12 |
T |
C |
5: 121,742,322 (GRCm39) |
T429A |
probably benign |
Het |
Afmid |
A |
C |
11: 117,727,300 (GRCm39) |
I275L |
probably benign |
Het |
Aimp1 |
A |
C |
3: 132,382,860 (GRCm39) |
D5E |
possibly damaging |
Het |
Aldob |
G |
A |
4: 49,538,171 (GRCm39) |
A319V |
probably benign |
Het |
Ankar |
C |
T |
1: 72,697,600 (GRCm39) |
V1068I |
possibly damaging |
Het |
Ccr2 |
C |
T |
9: 123,906,830 (GRCm39) |
S370L |
probably benign |
Het |
Chrnb4 |
A |
G |
9: 54,942,102 (GRCm39) |
Y391H |
probably damaging |
Het |
Clip1 |
A |
G |
5: 123,761,281 (GRCm39) |
M873T |
possibly damaging |
Het |
Cspg4 |
G |
C |
9: 56,797,762 (GRCm39) |
G1409R |
probably damaging |
Het |
Dnah17 |
A |
T |
11: 117,987,362 (GRCm39) |
L1320* |
probably null |
Het |
Dock4 |
T |
C |
12: 40,829,641 (GRCm39) |
|
probably benign |
Het |
Eml4 |
T |
C |
17: 83,717,622 (GRCm39) |
S65P |
probably benign |
Het |
Fblim1 |
A |
T |
4: 141,312,175 (GRCm39) |
D183E |
probably damaging |
Het |
Foxn1 |
T |
C |
11: 78,256,763 (GRCm39) |
|
probably benign |
Het |
Gm973 |
A |
T |
1: 59,601,930 (GRCm39) |
T515S |
possibly damaging |
Het |
Hdac7 |
G |
A |
15: 97,704,386 (GRCm39) |
Q495* |
probably null |
Het |
Hipk3 |
T |
C |
2: 104,301,518 (GRCm39) |
I225V |
probably benign |
Het |
Hrc |
A |
T |
7: 44,985,638 (GRCm39) |
D263V |
probably damaging |
Het |
Hs6st3 |
T |
C |
14: 119,375,888 (GRCm39) |
I21T |
probably benign |
Het |
Il15ra |
A |
G |
2: 11,728,334 (GRCm39) |
T133A |
possibly damaging |
Het |
Krt78 |
T |
C |
15: 101,854,603 (GRCm39) |
*1069W |
probably null |
Het |
Lama3 |
T |
A |
18: 12,586,920 (GRCm39) |
M761K |
probably damaging |
Het |
Macf1 |
T |
C |
4: 123,383,005 (GRCm39) |
T1320A |
probably damaging |
Het |
Mark3 |
A |
T |
12: 111,581,875 (GRCm39) |
I115L |
probably damaging |
Het |
Mcph1 |
T |
G |
8: 18,739,081 (GRCm39) |
|
probably benign |
Het |
Med23 |
T |
A |
10: 24,786,664 (GRCm39) |
N923K |
probably benign |
Het |
Msrb2 |
T |
G |
2: 19,398,032 (GRCm39) |
Y97D |
probably damaging |
Het |
Muc6 |
C |
T |
7: 141,234,368 (GRCm39) |
G708S |
probably damaging |
Het |
Mylk |
T |
C |
16: 34,700,673 (GRCm39) |
|
probably null |
Het |
Nfrkb |
T |
A |
9: 31,325,980 (GRCm39) |
V1141E |
possibly damaging |
Het |
Obscn |
T |
C |
11: 58,958,555 (GRCm39) |
E3675G |
probably damaging |
Het |
Or11h7 |
T |
A |
14: 50,890,821 (GRCm39) |
N42K |
probably damaging |
Het |
Or2l5 |
G |
A |
16: 19,333,586 (GRCm39) |
P267S |
probably damaging |
Het |
Or2t6 |
A |
T |
14: 14,175,446 (GRCm38) |
V212E |
probably damaging |
Het |
Or51aa2 |
A |
T |
7: 103,188,201 (GRCm39) |
F80Y |
probably damaging |
Het |
Or52z14 |
A |
G |
7: 103,253,219 (GRCm39) |
|
probably null |
Het |
Or5ac21 |
T |
C |
16: 59,124,091 (GRCm39) |
S193P |
probably damaging |
Het |
Or8k21 |
C |
G |
2: 86,145,498 (GRCm39) |
G44A |
probably damaging |
Het |
Pan2 |
T |
C |
10: 128,156,282 (GRCm39) |
V1171A |
probably damaging |
Het |
Pdgfc |
C |
T |
3: 81,116,552 (GRCm39) |
T302I |
probably damaging |
Het |
Pkhd1l1 |
G |
T |
15: 44,393,109 (GRCm39) |
V1815F |
probably damaging |
Het |
Pnpt1 |
A |
G |
11: 29,091,256 (GRCm39) |
I337V |
probably benign |
Het |
Psma8 |
T |
G |
18: 14,864,033 (GRCm39) |
|
probably null |
Het |
Rbl2 |
T |
C |
8: 91,812,090 (GRCm39) |
S220P |
probably benign |
Het |
Rere |
T |
A |
4: 150,700,190 (GRCm39) |
D1091E |
probably damaging |
Het |
Rpa1 |
A |
G |
11: 75,197,002 (GRCm39) |
C540R |
probably damaging |
Het |
Sema3d |
T |
A |
5: 12,613,285 (GRCm39) |
V454E |
probably damaging |
Het |
Sema3d |
T |
C |
5: 12,634,965 (GRCm39) |
V677A |
probably benign |
Het |
Sgk2 |
A |
G |
2: 162,846,080 (GRCm39) |
N207S |
probably benign |
Het |
Sirpb1a |
T |
C |
3: 15,444,141 (GRCm39) |
I370V |
probably benign |
Het |
Slc22a19 |
A |
G |
19: 7,661,224 (GRCm39) |
|
probably benign |
Het |
Slc26a1 |
T |
A |
5: 108,820,338 (GRCm39) |
D287V |
probably damaging |
Het |
Slc36a4 |
T |
A |
9: 15,645,506 (GRCm39) |
V311D |
probably damaging |
Het |
Slco1b2 |
A |
T |
6: 141,628,951 (GRCm39) |
Y551F |
probably damaging |
Het |
Slco2a1 |
T |
A |
9: 102,956,653 (GRCm39) |
Y488* |
probably null |
Het |
Stab2 |
A |
C |
10: 86,732,360 (GRCm39) |
|
probably null |
Het |
Strn |
T |
C |
17: 78,999,928 (GRCm39) |
|
probably null |
Het |
Tbxas1 |
A |
G |
6: 38,925,575 (GRCm39) |
|
probably benign |
Het |
Thumpd3 |
A |
G |
6: 113,032,838 (GRCm39) |
N192S |
possibly damaging |
Het |
Tns3 |
T |
A |
11: 8,385,738 (GRCm39) |
I1386F |
probably benign |
Het |
Treml4 |
T |
A |
17: 48,579,821 (GRCm39) |
V219E |
probably damaging |
Het |
Triobp |
T |
C |
15: 78,850,908 (GRCm39) |
V354A |
probably benign |
Het |
Tspan8 |
A |
G |
10: 115,680,035 (GRCm39) |
I217V |
probably benign |
Het |
Tub |
G |
A |
7: 108,627,042 (GRCm39) |
G314R |
possibly damaging |
Het |
Ube3b |
C |
T |
5: 114,537,926 (GRCm39) |
T339M |
possibly damaging |
Het |
Vmn2r43 |
A |
G |
7: 8,258,550 (GRCm39) |
I221T |
possibly damaging |
Het |
Vmn2r5 |
C |
T |
3: 64,411,642 (GRCm39) |
E309K |
probably damaging |
Het |
Zfp110 |
C |
T |
7: 12,582,429 (GRCm39) |
T359I |
probably benign |
Het |
Zfp322a |
A |
T |
13: 23,541,074 (GRCm39) |
C223S |
probably damaging |
Het |
Zfp512b |
G |
A |
2: 181,228,878 (GRCm39) |
R696* |
probably null |
Het |
|
Other mutations in Lonp1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00327:Lonp1
|
APN |
17 |
56,926,265 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00934:Lonp1
|
APN |
17 |
56,921,683 (GRCm39) |
missense |
probably benign |
0.21 |
IGL01065:Lonp1
|
APN |
17 |
56,922,500 (GRCm39) |
unclassified |
probably benign |
|
IGL01343:Lonp1
|
APN |
17 |
56,922,586 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL01734:Lonp1
|
APN |
17 |
56,923,026 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02141:Lonp1
|
APN |
17 |
56,922,086 (GRCm39) |
missense |
probably benign |
0.19 |
IGL02979:Lonp1
|
APN |
17 |
56,928,940 (GRCm39) |
missense |
probably benign |
0.02 |
chaney
|
UTSW |
17 |
56,929,515 (GRCm39) |
missense |
probably damaging |
1.00 |
Karloff
|
UTSW |
17 |
56,925,406 (GRCm39) |
missense |
probably benign |
|
R0015:Lonp1
|
UTSW |
17 |
56,925,406 (GRCm39) |
missense |
probably benign |
|
R0015:Lonp1
|
UTSW |
17 |
56,925,406 (GRCm39) |
missense |
probably benign |
|
R0863:Lonp1
|
UTSW |
17 |
56,925,331 (GRCm39) |
missense |
probably damaging |
1.00 |
R1343:Lonp1
|
UTSW |
17 |
56,927,272 (GRCm39) |
missense |
probably damaging |
1.00 |
R1735:Lonp1
|
UTSW |
17 |
56,921,956 (GRCm39) |
missense |
probably damaging |
1.00 |
R1976:Lonp1
|
UTSW |
17 |
56,922,068 (GRCm39) |
missense |
possibly damaging |
0.69 |
R1977:Lonp1
|
UTSW |
17 |
56,922,068 (GRCm39) |
missense |
possibly damaging |
0.69 |
R2484:Lonp1
|
UTSW |
17 |
56,921,659 (GRCm39) |
missense |
probably damaging |
1.00 |
R2895:Lonp1
|
UTSW |
17 |
56,922,562 (GRCm39) |
missense |
probably damaging |
1.00 |
R3123:Lonp1
|
UTSW |
17 |
56,933,488 (GRCm39) |
missense |
possibly damaging |
0.79 |
R3125:Lonp1
|
UTSW |
17 |
56,933,488 (GRCm39) |
missense |
possibly damaging |
0.79 |
R3429:Lonp1
|
UTSW |
17 |
56,925,337 (GRCm39) |
missense |
probably damaging |
1.00 |
R3726:Lonp1
|
UTSW |
17 |
56,925,310 (GRCm39) |
unclassified |
probably benign |
|
R3767:Lonp1
|
UTSW |
17 |
56,928,952 (GRCm39) |
missense |
possibly damaging |
0.80 |
R4618:Lonp1
|
UTSW |
17 |
56,929,511 (GRCm39) |
missense |
probably benign |
0.03 |
R4859:Lonp1
|
UTSW |
17 |
56,933,587 (GRCm39) |
missense |
probably benign |
0.00 |
R4951:Lonp1
|
UTSW |
17 |
56,927,335 (GRCm39) |
missense |
possibly damaging |
0.64 |
R5208:Lonp1
|
UTSW |
17 |
56,924,793 (GRCm39) |
missense |
probably damaging |
1.00 |
R5620:Lonp1
|
UTSW |
17 |
56,927,263 (GRCm39) |
missense |
probably benign |
0.05 |
R5621:Lonp1
|
UTSW |
17 |
56,927,263 (GRCm39) |
missense |
probably benign |
0.05 |
R5622:Lonp1
|
UTSW |
17 |
56,927,263 (GRCm39) |
missense |
probably benign |
0.05 |
R6131:Lonp1
|
UTSW |
17 |
56,921,457 (GRCm39) |
missense |
probably benign |
0.01 |
R6377:Lonp1
|
UTSW |
17 |
56,928,961 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6692:Lonp1
|
UTSW |
17 |
56,926,230 (GRCm39) |
missense |
probably damaging |
1.00 |
R7052:Lonp1
|
UTSW |
17 |
56,933,549 (GRCm39) |
missense |
probably benign |
0.31 |
R7131:Lonp1
|
UTSW |
17 |
56,924,814 (GRCm39) |
missense |
probably damaging |
1.00 |
R7295:Lonp1
|
UTSW |
17 |
56,929,495 (GRCm39) |
missense |
possibly damaging |
0.70 |
R7739:Lonp1
|
UTSW |
17 |
56,933,620 (GRCm39) |
missense |
probably benign |
|
R7792:Lonp1
|
UTSW |
17 |
56,929,515 (GRCm39) |
missense |
probably damaging |
1.00 |
R8307:Lonp1
|
UTSW |
17 |
56,933,573 (GRCm39) |
missense |
probably benign |
0.01 |
R8546:Lonp1
|
UTSW |
17 |
56,933,702 (GRCm39) |
missense |
probably benign |
0.00 |
R9257:Lonp1
|
UTSW |
17 |
56,927,516 (GRCm39) |
nonsense |
probably null |
|
R9586:Lonp1
|
UTSW |
17 |
56,924,839 (GRCm39) |
missense |
probably damaging |
1.00 |
|