Other mutations in this stock |
Total: 63 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
5530400C23Rik |
A |
G |
6: 133,271,202 (GRCm39) |
E82G |
possibly damaging |
Het |
Adra2a |
C |
G |
19: 54,035,454 (GRCm39) |
P270R |
probably benign |
Het |
Alox12b |
A |
T |
11: 69,054,812 (GRCm39) |
I272F |
possibly damaging |
Het |
Als2 |
C |
A |
1: 59,250,468 (GRCm39) |
E425D |
probably benign |
Het |
Arhgap21 |
C |
A |
2: 20,858,938 (GRCm39) |
C1252F |
possibly damaging |
Het |
Arhgap31 |
T |
G |
16: 38,423,976 (GRCm39) |
T697P |
probably damaging |
Het |
Aspm |
C |
A |
1: 139,385,523 (GRCm39) |
T389K |
probably benign |
Het |
B4galnt3 |
T |
A |
6: 120,209,905 (GRCm39) |
I73F |
probably damaging |
Het |
Btn2a2 |
A |
G |
13: 23,672,008 (GRCm39) |
V27A |
probably benign |
Het |
Cep97 |
A |
T |
16: 55,735,303 (GRCm39) |
N570K |
possibly damaging |
Het |
Cfh |
T |
C |
1: 140,036,266 (GRCm39) |
I751V |
probably benign |
Het |
Chd3 |
A |
G |
11: 69,241,046 (GRCm39) |
C1516R |
probably damaging |
Het |
Cul3 |
A |
G |
1: 80,258,576 (GRCm39) |
F487L |
probably damaging |
Het |
Dock1 |
T |
C |
7: 134,348,186 (GRCm39) |
S266P |
possibly damaging |
Het |
Dock6 |
A |
T |
9: 21,732,830 (GRCm39) |
Y1118* |
probably null |
Het |
Dolpp1 |
T |
A |
2: 30,282,515 (GRCm39) |
Y23N |
probably damaging |
Het |
Egf |
T |
C |
3: 129,511,617 (GRCm39) |
M517V |
probably benign |
Het |
Endou |
C |
A |
15: 97,609,969 (GRCm39) |
K442N |
probably damaging |
Het |
Fam210b |
C |
T |
2: 172,194,633 (GRCm39) |
R162W |
probably damaging |
Het |
Fbxw27 |
ATGT |
AT |
9: 109,602,322 (GRCm39) |
|
probably null |
Het |
Flt3 |
T |
A |
5: 147,291,442 (GRCm39) |
Q641L |
possibly damaging |
Het |
Ighv3-3 |
T |
A |
12: 114,160,270 (GRCm39) |
I47F |
probably damaging |
Het |
Il4 |
C |
T |
11: 53,504,837 (GRCm39) |
R76H |
probably damaging |
Het |
Inpp5f |
A |
C |
7: 128,278,515 (GRCm39) |
D435A |
possibly damaging |
Het |
Kcnq2 |
T |
G |
2: 180,729,407 (GRCm39) |
D532A |
probably damaging |
Het |
Krtap11-1 |
A |
C |
16: 89,368,062 (GRCm39) |
|
probably benign |
Het |
Lamp3 |
T |
A |
16: 19,494,832 (GRCm39) |
|
probably null |
Het |
Lcn3 |
A |
T |
2: 25,656,151 (GRCm39) |
I69L |
probably benign |
Het |
Lrrc43 |
A |
T |
5: 123,641,307 (GRCm39) |
H497L |
probably damaging |
Het |
Luc7l2 |
T |
G |
6: 38,580,315 (GRCm39) |
S305A |
unknown |
Het |
Malrd1 |
C |
T |
2: 15,640,809 (GRCm39) |
T513I |
unknown |
Het |
Mllt3 |
T |
A |
4: 87,759,418 (GRCm39) |
D210V |
probably damaging |
Het |
Mmp14 |
A |
G |
14: 54,673,251 (GRCm39) |
H53R |
possibly damaging |
Het |
Ndst4 |
A |
C |
3: 125,476,808 (GRCm39) |
H11P |
probably damaging |
Het |
Oas1c |
A |
G |
5: 120,946,202 (GRCm39) |
F99L |
probably benign |
Het |
Or10s1 |
T |
C |
9: 39,986,353 (GRCm39) |
L254P |
probably damaging |
Het |
Or1e35 |
T |
C |
11: 73,797,637 (GRCm39) |
K227R |
probably benign |
Het |
Or1j11 |
G |
T |
2: 36,311,784 (GRCm39) |
A125S |
probably damaging |
Het |
Or5w15 |
G |
A |
2: 87,568,644 (GRCm39) |
T8I |
probably benign |
Het |
Or7g25 |
T |
A |
9: 19,160,561 (GRCm39) |
I45F |
probably damaging |
Het |
Pappa2 |
C |
A |
1: 158,784,817 (GRCm39) |
Q64H |
probably damaging |
Het |
Pcdhb15 |
T |
C |
18: 37,608,948 (GRCm39) |
F727L |
probably benign |
Het |
Pcsk1 |
A |
T |
13: 75,259,039 (GRCm39) |
N271I |
probably damaging |
Het |
Pkhd1l1 |
G |
A |
15: 44,410,239 (GRCm39) |
G2582D |
probably damaging |
Het |
Psma4 |
A |
T |
9: 54,862,245 (GRCm39) |
Q123L |
probably damaging |
Het |
Selenbp2 |
A |
T |
3: 94,605,368 (GRCm39) |
I127F |
possibly damaging |
Het |
Shank1 |
G |
A |
7: 43,962,342 (GRCm39) |
S71N |
unknown |
Het |
Slc29a3 |
G |
T |
10: 60,551,960 (GRCm39) |
C361* |
probably null |
Het |
Slx4 |
C |
A |
16: 3,797,917 (GRCm39) |
R1489L |
probably damaging |
Het |
Sorl1 |
A |
C |
9: 41,993,105 (GRCm39) |
Y306* |
probably null |
Het |
Tbc1d16 |
G |
T |
11: 119,101,335 (GRCm39) |
H58Q |
probably damaging |
Het |
Tfdp2 |
A |
G |
9: 96,169,663 (GRCm39) |
T5A |
probably damaging |
Het |
Thbs1 |
G |
T |
2: 117,953,932 (GRCm39) |
G1061V |
probably damaging |
Het |
Timm29 |
G |
A |
9: 21,504,662 (GRCm39) |
R110H |
probably damaging |
Het |
Tmf1 |
C |
T |
6: 97,147,293 (GRCm39) |
E558K |
possibly damaging |
Het |
Trappc11 |
T |
C |
8: 47,972,713 (GRCm39) |
T287A |
possibly damaging |
Het |
Unc119b |
G |
A |
5: 115,272,827 (GRCm39) |
T48M |
probably benign |
Het |
Vmn1r123 |
T |
C |
7: 20,896,987 (GRCm39) |
I293T |
probably benign |
Het |
Vmn2r67 |
G |
A |
7: 84,786,317 (GRCm39) |
H563Y |
possibly damaging |
Het |
Vps8 |
G |
T |
16: 21,336,893 (GRCm39) |
V763L |
probably benign |
Het |
Wdr3 |
A |
T |
3: 100,050,752 (GRCm39) |
Y722* |
probably null |
Het |
Xrn1 |
A |
G |
9: 95,920,756 (GRCm39) |
T1339A |
probably benign |
Het |
Zfp827 |
T |
A |
8: 79,905,604 (GRCm39) |
H860Q |
probably damaging |
Het |
|
Other mutations in Nln |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00466:Nln
|
APN |
13 |
104,172,153 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01656:Nln
|
APN |
13 |
104,198,249 (GRCm39) |
splice site |
probably null |
|
R0025:Nln
|
UTSW |
13 |
104,173,399 (GRCm39) |
missense |
probably damaging |
0.98 |
R0294:Nln
|
UTSW |
13 |
104,189,087 (GRCm39) |
missense |
probably damaging |
1.00 |
R1396:Nln
|
UTSW |
13 |
104,198,261 (GRCm39) |
missense |
probably benign |
0.01 |
R1657:Nln
|
UTSW |
13 |
104,173,455 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2087:Nln
|
UTSW |
13 |
104,173,877 (GRCm39) |
missense |
probably damaging |
0.96 |
R2847:Nln
|
UTSW |
13 |
104,161,533 (GRCm39) |
missense |
probably damaging |
1.00 |
R3034:Nln
|
UTSW |
13 |
104,173,947 (GRCm39) |
missense |
possibly damaging |
0.91 |
R5576:Nln
|
UTSW |
13 |
104,195,338 (GRCm39) |
missense |
probably damaging |
1.00 |
R5585:Nln
|
UTSW |
13 |
104,161,569 (GRCm39) |
missense |
possibly damaging |
0.73 |
R5882:Nln
|
UTSW |
13 |
104,196,006 (GRCm39) |
missense |
probably benign |
0.08 |
R6763:Nln
|
UTSW |
13 |
104,172,163 (GRCm39) |
missense |
probably damaging |
1.00 |
R7209:Nln
|
UTSW |
13 |
104,209,406 (GRCm39) |
nonsense |
probably null |
|
R7347:Nln
|
UTSW |
13 |
104,187,355 (GRCm39) |
missense |
probably damaging |
0.96 |
R7417:Nln
|
UTSW |
13 |
104,173,478 (GRCm39) |
missense |
probably damaging |
1.00 |
R7467:Nln
|
UTSW |
13 |
104,161,530 (GRCm39) |
missense |
possibly damaging |
0.75 |
R7491:Nln
|
UTSW |
13 |
104,205,831 (GRCm39) |
missense |
probably damaging |
1.00 |
R7553:Nln
|
UTSW |
13 |
104,186,924 (GRCm39) |
frame shift |
probably null |
|
R7842:Nln
|
UTSW |
13 |
104,189,137 (GRCm39) |
missense |
probably benign |
|
R8842:Nln
|
UTSW |
13 |
104,209,486 (GRCm39) |
missense |
probably benign |
0.24 |
R9295:Nln
|
UTSW |
13 |
104,186,924 (GRCm39) |
frame shift |
probably null |
|
R9512:Nln
|
UTSW |
13 |
104,198,274 (GRCm39) |
missense |
possibly damaging |
0.89 |
R9606:Nln
|
UTSW |
13 |
104,186,924 (GRCm39) |
frame shift |
probably null |
|
X0020:Nln
|
UTSW |
13 |
104,198,318 (GRCm39) |
missense |
probably damaging |
1.00 |
|