Other mutations in this stock |
Total: 91 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
5330417H12Rik |
T |
C |
7: 107,223,897 (GRCm39) |
|
probably benign |
Het |
Adgrf2 |
T |
C |
17: 43,022,084 (GRCm39) |
I247V |
probably benign |
Het |
Adgrv1 |
A |
G |
13: 81,418,857 (GRCm39) |
|
probably null |
Het |
Ankrd22 |
T |
A |
19: 34,126,752 (GRCm39) |
K26I |
possibly damaging |
Het |
Arhgap32 |
T |
A |
9: 32,156,552 (GRCm39) |
|
probably null |
Het |
Armc10 |
A |
G |
5: 21,866,522 (GRCm39) |
Y262C |
probably damaging |
Het |
Arrb2 |
A |
G |
11: 70,330,725 (GRCm39) |
D374G |
probably benign |
Het |
Ascc3 |
C |
T |
10: 50,625,227 (GRCm39) |
R1675C |
probably damaging |
Het |
Atg5 |
T |
C |
10: 44,239,046 (GRCm39) |
*276R |
probably null |
Het |
Bcl11b |
G |
A |
12: 107,882,968 (GRCm39) |
T377M |
probably damaging |
Het |
C1s2 |
C |
A |
6: 124,612,073 (GRCm39) |
E104* |
probably null |
Het |
Carf |
A |
T |
1: 60,180,526 (GRCm39) |
H316L |
probably damaging |
Het |
Ccdc77 |
A |
T |
6: 120,311,796 (GRCm39) |
I234N |
probably damaging |
Het |
Cd300c2 |
A |
T |
11: 114,887,826 (GRCm39) |
V192E |
possibly damaging |
Het |
Cep72 |
G |
A |
13: 74,207,584 (GRCm39) |
R62C |
probably damaging |
Het |
Clasp1 |
T |
A |
1: 118,436,640 (GRCm39) |
L308* |
probably null |
Het |
Clec2g |
A |
G |
6: 128,956,411 (GRCm39) |
S25G |
probably benign |
Het |
Cngb1 |
T |
C |
8: 95,978,601 (GRCm39) |
M1046V |
probably damaging |
Het |
Cobll1 |
A |
T |
2: 64,928,037 (GRCm39) |
D1095E |
probably benign |
Het |
Cpeb2 |
A |
G |
5: 43,402,005 (GRCm39) |
H662R |
possibly damaging |
Het |
Cps1 |
A |
T |
1: 67,178,922 (GRCm39) |
T45S |
probably benign |
Het |
Cspp1 |
A |
G |
1: 10,152,553 (GRCm39) |
Q368R |
possibly damaging |
Het |
Dcaf6 |
C |
A |
1: 165,239,032 (GRCm39) |
|
probably null |
Het |
Dcst1 |
T |
C |
3: 89,257,814 (GRCm39) |
Y652C |
possibly damaging |
Het |
Elf5 |
T |
G |
2: 103,279,918 (GRCm39) |
Y225* |
probably null |
Het |
Ermap |
A |
C |
4: 119,046,015 (GRCm39) |
|
probably benign |
Het |
Fam186b |
A |
T |
15: 99,169,202 (GRCm39) |
V915D |
probably damaging |
Het |
Fbxo34 |
C |
A |
14: 47,766,911 (GRCm39) |
N90K |
probably benign |
Het |
Flnc |
A |
G |
6: 29,447,524 (GRCm39) |
E1109G |
probably damaging |
Het |
Flt1 |
C |
A |
5: 147,620,749 (GRCm39) |
A132S |
probably benign |
Het |
Gabpb2 |
A |
G |
3: 95,097,947 (GRCm39) |
V242A |
probably benign |
Het |
Gas2l3 |
CACTCGTCATACT |
CACT |
10: 89,266,820 (GRCm39) |
|
probably benign |
Het |
Gm21798 |
A |
T |
15: 64,689,732 (GRCm39) |
|
probably benign |
Het |
Gpr179 |
A |
T |
11: 97,237,487 (GRCm39) |
S345T |
possibly damaging |
Het |
Gusb |
A |
T |
5: 130,026,959 (GRCm39) |
F377L |
probably damaging |
Het |
Hnrnpu |
T |
C |
1: 178,156,938 (GRCm39) |
|
probably benign |
Het |
Htr3b |
C |
T |
9: 48,848,348 (GRCm39) |
|
probably null |
Het |
Iqub |
A |
T |
6: 24,501,368 (GRCm39) |
V194D |
probably damaging |
Het |
Itga2b |
A |
G |
11: 102,351,985 (GRCm39) |
V504A |
probably benign |
Het |
Itga4 |
T |
A |
2: 79,118,592 (GRCm39) |
F430L |
probably damaging |
Het |
Jcad |
C |
A |
18: 4,673,762 (GRCm39) |
P508H |
probably damaging |
Het |
Jph1 |
T |
C |
1: 17,161,835 (GRCm39) |
T276A |
probably damaging |
Het |
Kansl2 |
A |
G |
15: 98,429,771 (GRCm39) |
F87S |
possibly damaging |
Het |
Kdm1b |
T |
C |
13: 47,216,620 (GRCm39) |
|
probably null |
Het |
Kif5b |
C |
T |
18: 6,220,930 (GRCm39) |
D393N |
probably benign |
Het |
Kmt2d |
A |
T |
15: 98,747,420 (GRCm39) |
|
probably benign |
Het |
Krt75 |
A |
G |
15: 101,478,674 (GRCm39) |
I320T |
probably damaging |
Het |
Lhfpl7 |
T |
A |
5: 113,386,036 (GRCm39) |
M161K |
probably benign |
Het |
Lipo5 |
T |
C |
19: 33,443,348 (GRCm39) |
N156S |
unknown |
Het |
Mblac2 |
A |
C |
13: 81,859,706 (GRCm39) |
Q19P |
probably null |
Het |
Mdfic2 |
A |
T |
6: 98,215,080 (GRCm39) |
M181K |
probably damaging |
Het |
Mfsd4b3-ps |
T |
C |
10: 39,824,056 (GRCm39) |
H68R |
probably damaging |
Het |
Mzb1 |
A |
T |
18: 35,781,006 (GRCm39) |
|
probably null |
Het |
Nup210l |
T |
A |
3: 90,077,337 (GRCm39) |
I891N |
probably benign |
Het |
Nwd1 |
G |
A |
8: 73,398,841 (GRCm39) |
R667Q |
probably damaging |
Het |
Oas1h |
C |
T |
5: 121,005,172 (GRCm39) |
Q207* |
probably null |
Het |
Or13c7d |
A |
T |
4: 43,770,476 (GRCm39) |
F178L |
possibly damaging |
Het |
Pcdh15 |
C |
T |
10: 74,340,625 (GRCm39) |
R1120* |
probably null |
Het |
Pfkl |
A |
G |
10: 77,824,144 (GRCm39) |
L748P |
probably damaging |
Het |
Phldb2 |
T |
A |
16: 45,571,758 (GRCm39) |
K473N |
probably damaging |
Het |
Rapgef6 |
G |
A |
11: 54,443,662 (GRCm39) |
V82I |
probably damaging |
Het |
Rfc3 |
A |
T |
5: 151,570,960 (GRCm39) |
L112Q |
probably damaging |
Het |
Rsph6a |
T |
A |
7: 18,801,997 (GRCm39) |
C349S |
possibly damaging |
Het |
Sec16a |
A |
T |
2: 26,331,979 (GRCm39) |
|
probably benign |
Het |
Septin14 |
T |
A |
5: 129,770,030 (GRCm39) |
Y222F |
probably benign |
Het |
Skor2 |
T |
C |
18: 76,947,990 (GRCm39) |
S571P |
possibly damaging |
Het |
Slc13a5 |
T |
A |
11: 72,148,244 (GRCm39) |
M264L |
probably damaging |
Het |
Slc45a3 |
T |
A |
1: 131,909,315 (GRCm39) |
V504E |
probably damaging |
Het |
Smg1 |
C |
T |
7: 117,751,631 (GRCm39) |
|
probably benign |
Het |
Smim20 |
A |
G |
5: 53,434,503 (GRCm39) |
N45S |
probably null |
Het |
Spp2 |
A |
T |
1: 88,339,991 (GRCm39) |
S111C |
probably damaging |
Het |
Sspo |
A |
G |
6: 48,442,664 (GRCm39) |
|
probably null |
Het |
Sycp2 |
C |
T |
2: 178,045,450 (GRCm39) |
|
probably null |
Het |
Tas2r113 |
A |
G |
6: 132,870,521 (GRCm39) |
N183S |
possibly damaging |
Het |
Tcaf2 |
A |
T |
6: 42,606,679 (GRCm39) |
M425K |
probably benign |
Het |
Tdrp |
A |
G |
8: 14,003,845 (GRCm39) |
V164A |
possibly damaging |
Het |
Tmbim1 |
A |
G |
1: 74,328,568 (GRCm39) |
F298S |
probably damaging |
Het |
Tmem89 |
A |
G |
9: 108,743,829 (GRCm39) |
|
probably benign |
Het |
Trpm2 |
G |
T |
10: 77,768,023 (GRCm39) |
C825* |
probably null |
Het |
Tsc1 |
A |
G |
2: 28,565,201 (GRCm39) |
E421G |
possibly damaging |
Het |
Usp24 |
T |
C |
4: 106,245,834 (GRCm39) |
I1364T |
probably benign |
Het |
Vmn1r52 |
G |
A |
6: 90,155,930 (GRCm39) |
G78E |
possibly damaging |
Het |
Vmn2r73 |
T |
G |
7: 85,506,829 (GRCm39) |
I828L |
probably damaging |
Het |
Vwa5b1 |
A |
T |
4: 138,338,058 (GRCm39) |
D87E |
probably benign |
Het |
Zfp1010 |
T |
C |
2: 176,957,223 (GRCm39) |
T92A |
possibly damaging |
Het |
Zfp451 |
A |
T |
1: 33,844,465 (GRCm39) |
D47E |
probably damaging |
Het |
Zfp821 |
A |
G |
8: 110,450,841 (GRCm39) |
E278G |
probably damaging |
Het |
Zfp930 |
A |
T |
8: 69,681,597 (GRCm39) |
T430S |
probably benign |
Het |
Zfp994 |
G |
T |
17: 22,419,448 (GRCm39) |
Y500* |
probably null |
Het |
Zmat3 |
A |
T |
3: 32,397,836 (GRCm39) |
I142N |
probably damaging |
Het |
Zzef1 |
T |
A |
11: 72,792,214 (GRCm39) |
I2266N |
probably 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 |
R0128:Ablim2
|
UTSW |
5 |
35,966,520 (GRCm39) |
splice site |
probably benign |
|
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 |
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 |
|