Other mutations in this stock |
Total: 79 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A2ml1 |
A |
G |
6: 128,552,602 (GRCm39) |
|
probably benign |
Het |
Abcd4 |
T |
G |
12: 84,659,126 (GRCm39) |
Q210P |
possibly damaging |
Het |
Acte1 |
G |
T |
7: 143,445,492 (GRCm39) |
G178C |
probably damaging |
Het |
Actl6b |
A |
G |
5: 137,553,327 (GRCm39) |
N113S |
probably benign |
Het |
Actn3 |
A |
T |
19: 4,921,643 (GRCm39) |
V179E |
probably damaging |
Het |
Aff4 |
C |
A |
11: 53,306,293 (GRCm39) |
T1145N |
probably damaging |
Het |
Ankrd42 |
G |
A |
7: 92,241,067 (GRCm39) |
Q431* |
probably null |
Het |
Anxa9 |
A |
G |
3: 95,209,733 (GRCm39) |
S129P |
probably benign |
Het |
Arfgef2 |
T |
G |
2: 166,677,639 (GRCm39) |
I88S |
probably damaging |
Het |
Asap3 |
C |
A |
4: 135,961,915 (GRCm39) |
N285K |
probably damaging |
Het |
Atp6v0a2 |
A |
G |
5: 124,790,248 (GRCm39) |
N477S |
probably damaging |
Het |
Atp7b |
C |
T |
8: 22,518,188 (GRCm39) |
E205K |
possibly damaging |
Het |
Atp8b5 |
T |
A |
4: 43,369,715 (GRCm39) |
|
probably null |
Het |
C87436 |
G |
A |
6: 86,446,809 (GRCm39) |
G533D |
probably damaging |
Het |
Ccdc138 |
T |
A |
10: 58,364,182 (GRCm39) |
I314N |
probably damaging |
Het |
Ccs |
A |
G |
19: 4,875,654 (GRCm39) |
F237S |
probably damaging |
Het |
Ccz1 |
T |
G |
5: 143,946,112 (GRCm39) |
|
probably benign |
Het |
Cdcp2 |
C |
T |
4: 106,963,904 (GRCm39) |
|
probably benign |
Het |
Chd1 |
A |
G |
17: 17,613,829 (GRCm39) |
N531S |
probably damaging |
Het |
Clptm1 |
A |
T |
7: 19,368,932 (GRCm39) |
F476I |
probably damaging |
Het |
Colec12 |
C |
T |
18: 9,858,921 (GRCm39) |
P568L |
unknown |
Het |
Cped1 |
T |
A |
6: 22,121,038 (GRCm39) |
Y373N |
probably benign |
Het |
Cr2 |
A |
T |
1: 194,848,539 (GRCm39) |
V328D |
probably damaging |
Het |
D630045J12Rik |
A |
T |
6: 38,126,706 (GRCm39) |
|
probably benign |
Het |
Dcdc2a |
A |
T |
13: 25,371,655 (GRCm39) |
|
probably benign |
Het |
Dlg1 |
G |
T |
16: 31,676,883 (GRCm39) |
|
probably null |
Het |
Epb41l5 |
A |
C |
1: 119,477,632 (GRCm39) |
V705G |
possibly damaging |
Het |
Ergic3 |
C |
A |
2: 155,853,060 (GRCm39) |
R43S |
possibly damaging |
Het |
Flnb |
T |
C |
14: 7,901,951 (GRCm38) |
V938A |
probably damaging |
Het |
Frmd4a |
T |
C |
2: 4,608,903 (GRCm39) |
Y928H |
probably damaging |
Het |
Fyn |
C |
T |
10: 39,387,978 (GRCm39) |
T78M |
probably benign |
Het |
Gdap2 |
A |
G |
3: 100,109,311 (GRCm39) |
T443A |
probably damaging |
Het |
Ghrl |
A |
T |
6: 113,694,129 (GRCm39) |
|
probably benign |
Het |
Gm4787 |
T |
A |
12: 81,424,521 (GRCm39) |
K546* |
probably null |
Het |
Gm6576 |
C |
G |
15: 27,026,086 (GRCm39) |
|
noncoding transcript |
Het |
Got1 |
C |
T |
19: 43,512,816 (GRCm39) |
D27N |
probably benign |
Het |
Gucy2c |
C |
T |
6: 136,681,247 (GRCm39) |
V946I |
probably damaging |
Het |
Hectd4 |
T |
C |
5: 121,487,306 (GRCm39) |
Y3434H |
possibly damaging |
Het |
Hp1bp3 |
C |
T |
4: 137,964,520 (GRCm39) |
S348F |
probably damaging |
Het |
Itpr1 |
A |
G |
6: 108,448,170 (GRCm39) |
|
probably benign |
Het |
Kctd1 |
G |
A |
18: 15,107,237 (GRCm39) |
P743S |
probably benign |
Het |
Klhl23 |
T |
C |
2: 69,664,310 (GRCm39) |
V553A |
probably damaging |
Het |
Krt24 |
T |
C |
11: 99,171,093 (GRCm39) |
D495G |
probably damaging |
Het |
L3hypdh |
C |
T |
12: 72,123,917 (GRCm39) |
|
probably null |
Het |
Lipo3 |
C |
T |
19: 33,534,506 (GRCm39) |
|
probably null |
Het |
Lman2l |
G |
T |
1: 36,463,945 (GRCm39) |
S171* |
probably null |
Het |
Lrp1b |
T |
C |
2: 41,401,520 (GRCm39) |
D378G |
probably damaging |
Het |
Map3k4 |
T |
A |
17: 12,466,950 (GRCm39) |
D1104V |
probably damaging |
Het |
Mpeg1 |
T |
C |
19: 12,438,587 (GRCm39) |
V15A |
probably benign |
Het |
Narf |
C |
T |
11: 121,141,662 (GRCm39) |
R356C |
probably damaging |
Het |
Nebl |
T |
A |
2: 17,397,834 (GRCm39) |
Q487H |
possibly damaging |
Het |
Olfm5 |
G |
A |
7: 103,810,133 (GRCm39) |
A76V |
probably benign |
Het |
Or1j11 |
T |
A |
2: 36,312,299 (GRCm39) |
D296E |
probably benign |
Het |
Or2z8 |
C |
T |
8: 72,812,244 (GRCm39) |
T240M |
probably damaging |
Het |
Or52p1 |
A |
T |
7: 104,267,788 (GRCm39) |
I301F |
probably damaging |
Het |
Or5ak22 |
T |
A |
2: 85,230,305 (GRCm39) |
S191C |
probably damaging |
Het |
Or8k40 |
T |
C |
2: 86,584,231 (GRCm39) |
M284V |
probably benign |
Het |
Palb2 |
A |
T |
7: 121,727,389 (GRCm39) |
Y160* |
probably null |
Het |
Pasd1 |
T |
C |
X: 70,983,161 (GRCm39) |
C378R |
possibly damaging |
Het |
Paxip1 |
C |
T |
5: 27,949,183 (GRCm39) |
|
probably benign |
Het |
Pclo |
A |
G |
5: 14,729,811 (GRCm39) |
|
probably benign |
Het |
Pdcd11 |
G |
A |
19: 47,108,301 (GRCm39) |
V1223I |
probably benign |
Het |
Pde6c |
T |
C |
19: 38,157,813 (GRCm39) |
|
probably benign |
Het |
Prr12 |
A |
G |
7: 44,699,463 (GRCm39) |
|
probably benign |
Het |
Prss39 |
T |
A |
1: 34,541,281 (GRCm39) |
|
probably benign |
Het |
Samd5 |
A |
G |
10: 9,550,683 (GRCm39) |
W9R |
probably damaging |
Het |
Sfr1 |
A |
G |
19: 47,723,457 (GRCm39) |
*320W |
probably null |
Het |
Sft2d1rt |
A |
G |
11: 45,943,120 (GRCm39) |
M1T |
probably null |
Het |
Sh3bp4 |
A |
G |
1: 89,073,036 (GRCm39) |
N628S |
possibly damaging |
Het |
Sim1 |
A |
T |
10: 50,784,057 (GRCm39) |
I104F |
probably damaging |
Het |
Slc1a3 |
T |
C |
15: 8,665,693 (GRCm39) |
M519V |
probably benign |
Het |
Smcp |
T |
A |
3: 92,491,827 (GRCm39) |
T7S |
unknown |
Het |
Sp4 |
A |
G |
12: 118,264,551 (GRCm39) |
|
probably benign |
Het |
Spag9 |
T |
A |
11: 93,984,365 (GRCm39) |
I327N |
probably damaging |
Het |
Thbs4 |
G |
T |
13: 92,890,918 (GRCm39) |
H850N |
probably benign |
Het |
Ubap2l |
A |
T |
3: 89,928,680 (GRCm39) |
S478T |
possibly damaging |
Het |
Unc79 |
A |
G |
12: 103,054,693 (GRCm39) |
|
probably benign |
Het |
Vmn2r85 |
A |
G |
10: 130,255,054 (GRCm39) |
|
probably benign |
Het |
Wrap73 |
A |
G |
4: 154,226,957 (GRCm39) |
D19G |
possibly damaging |
Het |
|
Other mutations in Ablim2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00939:Ablim2
|
APN |
5 |
35,981,359 (GRCm39) |
unclassified |
probably benign |
|
IGL00945:Ablim2
|
APN |
5 |
35,994,364 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02439:Ablim2
|
APN |
5 |
36,015,206 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL02664:Ablim2
|
APN |
5 |
36,006,860 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02897:Ablim2
|
APN |
5 |
35,990,470 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03034:Ablim2
|
APN |
5 |
35,985,509 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03096:Ablim2
|
APN |
5 |
36,040,743 (GRCm39) |
nonsense |
probably null |
|
IGL03384:Ablim2
|
APN |
5 |
36,032,216 (GRCm39) |
missense |
probably damaging |
1.00 |
R0130:Ablim2
|
UTSW |
5 |
35,966,520 (GRCm39) |
splice site |
probably benign |
|
R0212:Ablim2
|
UTSW |
5 |
36,006,254 (GRCm39) |
splice site |
probably null |
|
R0344:Ablim2
|
UTSW |
5 |
35,994,277 (GRCm39) |
splice site |
probably benign |
|
R0675:Ablim2
|
UTSW |
5 |
36,024,124 (GRCm39) |
splice site |
probably benign |
|
R0788:Ablim2
|
UTSW |
5 |
36,015,245 (GRCm39) |
missense |
probably benign |
0.01 |
R1148:Ablim2
|
UTSW |
5 |
35,966,605 (GRCm39) |
missense |
probably damaging |
1.00 |
R1148:Ablim2
|
UTSW |
5 |
35,966,605 (GRCm39) |
missense |
probably damaging |
1.00 |
R1493:Ablim2
|
UTSW |
5 |
35,966,605 (GRCm39) |
missense |
probably damaging |
1.00 |
R1809:Ablim2
|
UTSW |
5 |
36,000,614 (GRCm39) |
intron |
probably benign |
|
R2070:Ablim2
|
UTSW |
5 |
35,955,857 (GRCm39) |
missense |
probably damaging |
1.00 |
R2163:Ablim2
|
UTSW |
5 |
35,959,697 (GRCm39) |
splice site |
probably benign |
|
R3962:Ablim2
|
UTSW |
5 |
35,969,519 (GRCm39) |
missense |
probably damaging |
1.00 |
R4852:Ablim2
|
UTSW |
5 |
35,959,766 (GRCm39) |
missense |
possibly damaging |
0.85 |
R4853:Ablim2
|
UTSW |
5 |
35,959,766 (GRCm39) |
missense |
possibly damaging |
0.85 |
R4854:Ablim2
|
UTSW |
5 |
35,959,766 (GRCm39) |
missense |
possibly damaging |
0.85 |
R4855:Ablim2
|
UTSW |
5 |
35,959,766 (GRCm39) |
missense |
possibly damaging |
0.85 |
R4866:Ablim2
|
UTSW |
5 |
35,959,766 (GRCm39) |
missense |
possibly damaging |
0.85 |
R4867:Ablim2
|
UTSW |
5 |
35,959,766 (GRCm39) |
missense |
possibly damaging |
0.85 |
R4906:Ablim2
|
UTSW |
5 |
35,959,766 (GRCm39) |
missense |
possibly damaging |
0.85 |
R4908:Ablim2
|
UTSW |
5 |
35,959,766 (GRCm39) |
missense |
possibly damaging |
0.85 |
R4909:Ablim2
|
UTSW |
5 |
35,959,766 (GRCm39) |
missense |
possibly damaging |
0.85 |
R4927:Ablim2
|
UTSW |
5 |
35,959,766 (GRCm39) |
missense |
possibly damaging |
0.85 |
R5210:Ablim2
|
UTSW |
5 |
35,994,416 (GRCm39) |
missense |
probably benign |
0.44 |
R5225:Ablim2
|
UTSW |
5 |
36,024,115 (GRCm39) |
splice site |
probably null |
|
R5439:Ablim2
|
UTSW |
5 |
36,015,170 (GRCm39) |
missense |
probably damaging |
0.98 |
R5528:Ablim2
|
UTSW |
5 |
36,013,510 (GRCm39) |
nonsense |
probably null |
|
R5629:Ablim2
|
UTSW |
5 |
36,014,507 (GRCm39) |
missense |
probably benign |
0.01 |
R5653:Ablim2
|
UTSW |
5 |
36,040,756 (GRCm39) |
missense |
probably damaging |
1.00 |
R5921:Ablim2
|
UTSW |
5 |
35,969,555 (GRCm39) |
missense |
probably damaging |
1.00 |
R6059:Ablim2
|
UTSW |
5 |
36,014,508 (GRCm39) |
missense |
probably benign |
0.37 |
R6241:Ablim2
|
UTSW |
5 |
36,032,241 (GRCm39) |
missense |
probably damaging |
1.00 |
R7492:Ablim2
|
UTSW |
5 |
35,998,673 (GRCm39) |
missense |
probably benign |
0.14 |
R7562:Ablim2
|
UTSW |
5 |
36,030,563 (GRCm39) |
missense |
probably benign |
0.00 |
R7960:Ablim2
|
UTSW |
5 |
36,014,493 (GRCm39) |
missense |
probably benign |
0.01 |
R8414:Ablim2
|
UTSW |
5 |
36,032,235 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8557:Ablim2
|
UTSW |
5 |
35,985,483 (GRCm39) |
missense |
probably damaging |
1.00 |
R8690:Ablim2
|
UTSW |
5 |
36,030,518 (GRCm39) |
missense |
possibly damaging |
0.48 |
R8710:Ablim2
|
UTSW |
5 |
36,030,518 (GRCm39) |
missense |
possibly damaging |
0.48 |
R8713:Ablim2
|
UTSW |
5 |
36,030,518 (GRCm39) |
missense |
possibly damaging |
0.48 |
R9059:Ablim2
|
UTSW |
5 |
35,959,850 (GRCm39) |
missense |
probably damaging |
1.00 |
R9452:Ablim2
|
UTSW |
5 |
36,015,198 (GRCm39) |
missense |
probably benign |
0.00 |
R9622:Ablim2
|
UTSW |
5 |
36,006,889 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Ablim2
|
UTSW |
5 |
36,006,202 (GRCm39) |
missense |
possibly damaging |
0.84 |
Z1177:Ablim2
|
UTSW |
5 |
35,998,637 (GRCm39) |
small deletion |
probably benign |
|
Z1177:Ablim2
|
UTSW |
5 |
35,981,387 (GRCm39) |
missense |
probably damaging |
0.98 |
Z1188:Ablim2
|
UTSW |
5 |
35,994,367 (GRCm39) |
missense |
probably damaging |
1.00 |
|